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Mesenchymal stem cell therapy for liver disease: full of chances and challenges

Cell & Bioscience volume 10, Article number: 123 (2020) Cite this article

Abstract

Liver disease is a major health problem that endangers human health worldwide. Currently, whole organ allograft transplantation is the gold standard for the treatment of end-stage liver disease. A shortage of suitable organs, high costs and surgical complications limit the application of liver transplantation. Mesenchymal stem cell therapy has been considered as a promising alternative approach for end-stage liver disease. Some clinical trials have confirmed the effectiveness of MSC therapy for liver disease, but its application has not been promoted and approved. There are still many issues that should be solved prior to using MSC therapy in clinical applications. The types of liver disease that are most suitable for MSC application should be determined, and the preparation and engraftment of MSCs should be standardized. These may be bottlenecks that limit the use of MSCs. We investigated 22 completed and several ongoing clinical trials to discuss these questions from a clinical perspective. We also discussed the important mechanisms by which MSCs play a therapeutic role in liver disease. Finally, we also proposed novel prospective approaches that can improve the therapeutic effect of MSCs.

Background

With high morbidity and mortality, liver disease presents a major threat to human health. Many stimuli, such as viral hepatitis, alcohol abuse, drugs, metabolic diseases, and autoimmune attack, can trigger chronic/acute liver injury and inflammation, which result in liver failure, cirrhosis and associated hepatocellular carcinoma. Orthotopic liver transplantation is the only effective treatment for liver cirrhosis and liver failure. However, the number of suitable donor organs is very limited. Adults on the waiting list for liver transplantation suffer from a mortality rate of almost 11% [1]. Patients are too weak to wait for suitable donor organs, so the best opportunity for treatment is missed. In addition, liver transplantation is expensive and not available for all patients. There is an urgent need to search for a more effective and feasible treatment for patients with liver cirrhosis and liver failure.

At present, cell therapy with hepatocytes, hemopoietic cells, immune cells, endothelial progenitor cells and mesenchymal stem cells has been suggested to be a promising candidate therapy for liver diseases [2]. A large body of studies investigated their advantages and disadvantages (Table 1). Among the cell types, MSCs have been the most promising cells because of their many advantages. (1) MSCs can be isolated easily from a wide variety of tissues and can be expanded in vitro without changing their properties. (2) MSCs can be injected into patients by allogeneic transplantation because of their low immunogenicity. Therefore, we can generate reserves of MSCs that we can give to patients at any time. (3) MSCs have the properties of self-renewal and can differentiate into multiple cell types. (4) Researchers have also shown the robust immunomodulation of MSCs. (5) MSCs can also produce secretomes, including soluble factors and exosomes, which can favor regeneration and injury repair. (6) Most importantly, MSCs can migrate to injury sites where they can exert protective effects. Therefore, MSCs have been used to treat various tissue injuries and immune-related diseases in clinical trials. To date, 321 completed clinical trials using MSCs were summarized in Fig. 1 according to the website https://clinicaltrials.gov/. Among them, bone/cartilage, brain/Nero and immune-related diseases account for almost 50% of all MSC-based clinical trials. In addition, we have noticed that 16 clinical trials are related to liver-related diseases. For liver diseases, however, both tissue damage and overactivation of inflammation always go hand in hand. Therefore, from every perspective, MSCs would be the best candidate for cell therapy of liver diseases. However, there are still many issues, and any confusion should be resolved before MSC application in the clinic.

Table1 Advantages and disadvantages among different cell types for the treatment of liver diseases
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Fig. 1
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Completed clinical trials based on MSC therapy by disease classification (n = 321)

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In this review, several issues that must be addressed during clinical treatment of MSCs are discussed from clinical perspectives. (1) Which kind of liver disease is most suitable for MSC application? (2) How should we choose the best source of MSCs, best doses of MSCs and best engraftment route of MSCs? (3) What are the mechanisms by which MSCs play a therapeutic role in liver disease? (4) Finally, we propose potential approaches to enhance the therapeutic effect of MSCs, including the use of modified MSCs, pretreated MSCs and cell-free therapy with MSCs. To address these issues, we examined both ongoing and published clinical trials of MSC applications in liver diseases. Some preclinical tests were also used to assist in drawing a conclusion. We would like to clear up any confusion about MSC applications in liver diseases and help patients receive more appropriate treatment. This review is intended to be beneficial for creating a new strategy for MSC application and enhancing the therapeutic effect of MSCs. It will also help to develop a more specific standard for MSC application.

Which kind of liver disease is most suitable for MSC application in the clinic?

MSCs have been shown to exert beneficial effects in a range of clinical settings, including the treatment of degenerative and immune-mediated diseases while also being reported to ameliorate liver injury in the setting of both acute and chronic liver damage. However, whether MSC-based therapy is more effective than conventional treatment and which type of liver disease is best suitable for MSCs application in clinic remained unclear.

To find out the indications of MSCs in the treatment of liver disease. In this review, we collected a total of 22 clinical trial articles on MSCs treatment for liver disease published from 2007 to 2018 (Table 2). As shown in the pie chart in Fig. 2a, 14 of them are about MSCs therapy for liver cirrhosis. The other five articles are related to liver failure, and three of them are related to complications after liver transplantation. We found that most of these diseases have a common feature, that is, they are all end-stage liver diseases. And for them, the only effective approach is organ transplantation, but its practical application is constrained by some well-known reasons such as the limited availability of donor organs, surgical complications, immunological side effects, and high medical cost [3]. The development of alternative methods for treatment of liver disease is highly requested. Therefore, stem cell therapy, and regenerative medicine are being investigated to improve the prognosis of patients with those end-stage liver diseases. Evaluation of the end points in these studies revealed the safety and efficacy of human MSC transplantation. While there are some differences in the therapeutic effects of different types of liver diseases.

Table 2 Clinical trials using MSCs to treat liver disease
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MSC therapy for liver cirrhosis

Liver cirrhosis (LC) is a complication of liver disease that involves the loss of liver cells and irreversible scarring of the liver. In the 14 articles, patients with cirrhosis caused by many forms of liver disease, such as chronic viral hepatitis (n = 5), chronic alcohol abuse (n = 2), primary biliary cirrhosis (n = 1), autoimmune hepatitis (n = 1) and other conditions (n = 5 heterogeneous cirrhosis), were included. We believe that the experimental results related to LC caused by viral hepatitis are the most convincing because 4 articles contained large samples of data and control groups. In two of the clinical studies mentioned above that were published in 2012, 30 patients with chronic hepatitis B-related LC and 15 patients with chronic hepatitis C-related LC received MSC transfusion. In both studies, compared to the control group, the patients transplanted with MSCs showed significantly improved liver function, as indicated by the elevation of serum albumin levels, a decrease in total serum bilirubin levels, and a decrease in the sodium model for end-stage liver disease score (MELD score) [4, 5]. Consistent with the above study, two other clinical trials related to LC caused by hepatitis B were carried out by different research institutes and clarified that MSC transplantation further improved the liver function, MELD scores and Child–Pugh classification of patients [6, 7]. In the trials conducted by Fang, as many as 103 patients were recruited to participate in the studies; 50 were in the transplant group, and the other patients were in the control group. Controlled trials with larger cohorts of patients have further confirmed the feasibility of MSC transplantation therapy for virus-related cirrhosis.

However, not all studies have revealed MSCs to have the desired treatment effect on liver cirrhosis. Mohamadnejad et al. [8] enrolled a total of 27 patients with decompensated cirrhosis and ruled out viral-associated cirrhosis. The patients in this pilot study were heterogeneous regarding the etiology of liver cirrhosis. The results showed that at the 12 months follow-up, the absolute changes in the Child scores, MELD scores, serum albumin, international normalized ratio (INR), serum transaminases and liver volumes did not differ significantly between the MSC and placebo groups. This indicates that based on this randomized controlled trial, autologous bone marrow MSC transplantation through the peripheral vein probably has no beneficial effect in cirrhotic patients. However, based on the above discussion, MSC therapy has a positive effect on patients with viral-associated cirrhosis. Thus, we speculated that there may be a certain correlation between the therapeutic effect of MSCs and the cause of cirrhosis. Interestingly, previous work reported in 2009 by the same author showed that 2 months after MSC injection, all patients had an improved general condition, quality of life and liver function [9]. Why are the results of these two studies completely contradictory? We note that the beneficial effects of MSC transplantation shown in the report published in 2009 are based on the absence of control experiments. Even if we observed improvement, we could not claim that such improvement is definitely related to MSC transplantation. It proved that the controlled trial is critical to the reliability of clinical trial results. Thus, clinical trials associated with heterogeneous LC that lack a control group have not been explored in depth here.

Furthermore, another phase 2 trial with a control group was related to alcoholic cirrhosis. Fifty-five patients (18 in the control group, 18 in the one-time MSC group, and 19 in the two-time MSC group) completed the study. In the fibrosis quantification (before versus after), the one-time and two-time BM-MSC groups were associated with 25% and 37% reductions in the proportion of the collagen area following BM-MSC therapy, respectively. While no significant change in fibrosis quantification was observed in the control group. These results were further confirmed by the Laennec fibrosis score and Child–Pugh score [10]. In summary, judging from existing clinical trial articles, MSC treatment may serve as a potential supplementary therapeutic tool to improve liver function in patients with viral-related cirrhosis and alcoholic cirrhosis.

To date, only a few large controlled trials have been conducted to treat liver cirrhosis patients with MSC transplantation. Several articles related to LC with a small amount of data or a lack of a control trial also showed positive treatment effects for MSCs, which indicated that MSC therapy is also promising for the treatment of cirrhosis induced by other factors, such as autoimmune hepatitis and primary biliary cirrhosis; however, larger samples and double-blind controlled trials are needed for further verification [11, 12].

MSC therapy for liver failure

Liver failure is a major health problem worldwide due to the variety of acute or chronic injuries that are induced by alcohol consumption, hepatotoxic drugs, autoimmune attack of hepatocytes, or infection with viruses, such as hepatitis B virus (HBV) and hepatitis C virus (HCV) [13]. In China, HBV infection accounts for the highest proportion of liver failure cases. Therefore, Peng et al. [14] enrolled 53 patients with liver failure caused by hepatitis B, who underwent MSC transplantation (105 patients served as the control group). The results showed that MSC transplantation is safe for patients with liver failure caused by chronic hepatitis B. The short-term efficacy was favorable, but long-term outcomes were not markedly improved. This is in agreement with the results of Shi et al. and Lin et al. who reported trials of MSC transfusion for acute-on-chronic liver failure (ACLF) patients in 2012 and 2017, respectively. In both trials, all the patients tolerated the transplantation well until the end of the follow-up period. MSC infusion is convenient for patients with HBV-related ACLF and significantly increases the survival rate by improving liver function and decreasing the incidence of severe infections [15, 16].

In addition to hepatitis B, hepatitis C is also a major form of viral hepatitis that has a very high incidence in Egypt. Therefore, a research institute in Egypt reported a trial that used autologous MSC-derived hepatocyte-like cells for end-stage liver failure therapy. The transplantation group showed improved liver function, including increases in serum albumin, Child–Pugh scores, MELD scores, and performance status, versus the controls [17]. Additionally, for patients with HCV-related end-stage liver disease, another study in Egypt provided evidence that administration of MSCs followed by granulocyte colony stimulating factor (GCSF) mobilization is excellent for liver stem cell therapy to retain liver mass and restore liver functions [18]. In summary, the above large controlled trials demonstrated that MSCs play a supportive role in the treatment of liver failure and show satisfactory tolerability and beneficial effects on liver synthetic functions and hepatic fibrosis resolution.

MSC therapy for complications of liver transplantation

Orthotopic liver transplantation is the only curative measure for patients with end-stage liver failure. However, the risk of complications after liver transplantation is still high, even with increases in surgical expertise. Two of the most common complications following liver transplant are rejection and infection. MSCs offer new therapeutic opportunities to prevent and treat solid organ transplant rejection. A recent pilot study demonstrated that UC-MSC therapy can alleviate liver damage and improve allograft histology in liver transplant patients with acute graft rejection who did not respond to immunosuppressive agent dose adjustments. However, the study was not carried out long enough to determine whether decreased infection resulted from MSC infusion [19].

However, in the same year, Detry et al. [20] enrolled 10 liver transplant patients to receive MSCs infusion and another 10 patients acted as controls. It was shown that no difference in the overall rates of rejection or graft survival was observed between the MSC infusion group and the control group. And Month-6 biopsies did not demonstrate a difference between groups. The study indicated that the immunosuppression weaning in MSC recipients was not successful. The results are completely different and contradictory compared to those of the above pilot study. We analyze that the possible reason might be that the aim and experimental design of the two studies were different. The pilot study aimed to examine the clinical feasibility of MSC infusion as a therapeutic option for liver allograft rejection, and all patients were treated with conventional immunosuppressive agents in both the experimental and control groups, showing the supportive effect of MSC infusion. The study reported by Detry et al. aimed to evaluate the feasibility and tolerability of a single infusion of MSCs in liver transplant recipients, and progressive immunosuppressive withdrawal was attempted in stable patients who received MSCs, which ultimately failed to promote tolerance. Therefore, we speculate that perhaps in the presence of immunosuppressive agents, MSCs can enhance the overall immunosuppressive effect; when the immunosuppressive agents are withdrawn, MSCs cannot serve alone as an alternative treatment. Another reason for this may be that the enrolled patients in the two studies were not truly similar. In the pilot study, the patients were considered suitable if their liver function did not respond to adjustment of immunosuppressive agents. These patients may be more sensitive to MSC application. Therefore, in the clinical application of MSCs, not only the use of an appropriate disease type but also the use of appropriate enrolled patients and a reasonable experimental protocol design should be considered.

Besides, 56 establishment of practical applications of MSCs involve clinical trials to investigate their therapeutic potential for treatment of liver disease, which also almost including decompensated liver cirrhosis, liver failure and complications after liver transplantation, according to ClinicalTrials.gov (Fig. 2b). And Based on the data from the published clinical trials we discussed above, combined with the relevant basic research we have carried out and some of the currently approved MSC-based products for clinical applications, we believe that MSCs are likely to be more effective in the treatment of inflammation-related liver diseases and liver transplant rejection complications.

Fig. 2
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The number and percentage of MSC based completed (a) and ongoing (b) clinical trials classified by liver disease type

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Preparation and engraftment of MSCs

Sources of MSCs

Mesenchymal stem cells were first obtained from bone marrow (BM) in 1970 [21], and they are now found to reside in various tissues apart from BM, including adipose tissue [22], umbilical cord (UC) [23], umbilical cord blood [24], placenta [25], amniotic fluid [26], amniotic membrane [27], dental pulp [28], synovium [29], peripheral blood, liver, lung [30], skeletal muscle [31, 32], hair follicles [33] and many others. Currently, MSCs applied for liver disease treatment in the clinic are isolated mostly from the umbilical cord and bone marrow, and in only a few cases adipose and menstrual blood-derived MSCs have been used (Fig. 3a). This is probably because BM-MSCs and UC-MSCs are most thoroughly studied types of cells, and BM and UC are relatively easy to obtain. However, there is still no definite standard for which source of MSCs should be used for clinical application. Many factors should be considered.

Fig. 3
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The number and percentage of MSC based clinical trials classified by sources (a) and transplantation routes (b) of MSCs

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BM-MSCs are most suitable for autologous transplantation. However, BM-MSCs have several limitations that should be considered. First, the invasive isolation method is a risk to patients, even to healthy donors, because invasion causes an injury that could lead to inflammation. The proportion of MSCs in bone marrow is not always very high, and they are difficult to proliferate in vitro [34]. In addition, fresh bone marrow from young donors is very limited. Most BM-MSC injections involve autologous transplantation in the clinic. Thus, the condition of patients also limits the number and potential of MSCs. For instance, age-related declines in proliferation and differentiation may weaken the therapeutic effect of MSCs [35].

However, UC-MSCs have many advantages. The isolation process used to obtain MSCs from UC does not cause damage, and it allows for utilization of tissue that might otherwise have been thrown away. It has been reported that the proliferation ability of UC-MSCs is much higher than that of BM-MSCs, [36] which fulfills the need for the large quantities required in the clinic. UC is at an early phase of organic development, so UC-MSCs show higher self-renewal and differentiation capacity [37]. Thus, there is no need to be concerned about age-related issues. On the other hand, UC-MSCs are better for liver failure treatment because of higher differentiation capacity. In addition, it has been demonstrated that the immunogenicity of UC-MSCs is lower than that of BM-MSCs [38, 39]. Thus, for patients with liver transplantation, autologous BM-MSCs and allogenic UC-MSCs are more appropriate. Adipose tissue is also easy to obtain, and the isolation method is very simple. However, AD-MSCs have been shown to have poor proliferation and self-renewal ability. Their anti-inflammatory ability is lower than that of BM-MSCs [40]. In conclusion, UC-MSCs are a prominent and preferred candidate for clinical application.

During clinical treatment, the choice between autologous or allogeneic transplantation is a source of confusion for doctors. For autologous transplantation, the type and amounts of MSC-derived tissues are very limited. Therefore, it will take a long time to obtain a sufficient number of MSCs for transplantation. The wait for cells might cause doctors to miss the window for treatment for liver diseases such as liver failure and acute liver failure. Obviously, the process of obtaining tissue also causes injury to patients. On the other hand, due to their lower immunogenicity, allogeneic MSCs can be injected without rejection risk, and an enough MSCs can be obtained very quickly. We can also choose the MSCs with the best properties. Therefore, allogeneic MSCs may be much better than autologous MSCs.

Routes of MSC transplantation

In clinical trials, MSCs have been transplanted into patients via various available routes; most are transplanted by intravenous injection, followed by intrahepatic injection (including via the portal vein and hepatic artery), and the least used method is intrasplenic injection (Fig. 3b). Which route is the best and most beneficial for therapy? How can the best route be chosen from all routes? It is indeed necessary to explore this question.

There are only a few completed clinical trials that have used multiple infusion routes simultaneously. In one clinical trial that used BM-MSCs to treat end-stage liver failure that was performed in Egypt, MSCs were injected into patients by the portal vein and intrasplenic injection, and the effects of these two injection routes for 6 months after transplantation were compared [17]. As a result, it was found that portal vein injection was more effective than intrasplenic injection, as indicated by the fatigue impact scale and MELD score. However, this effect was observed only in the first month, and the difference disappeared in the following days. This suggests that portal injection favors faster engraftment of injected cells but does not affect the total number of engrafted cells. Splenic injection is much easier than intrahepatic injection technically. However, we need to consider the complications induced by intrasplenic injection. Seventy percent of patients with intrasplenic injection had fever after cell transplantation, and 30% of patients had fever after intrahepatic injection. Thus, we prefer portal vein injection between these two injection routes.

Apart from portal vein injection, the hepatic artery can be used for intrahepatic injection. Hepatic artery injection is used more often than portal vein injection during MSC transplantation in clinical trials. However, is hepatic artery injection better than portal vein injection? Sang et al. concluded that intraportal injection was better for repairing liver injury in swine with ALF than hepatic intra-arterial injection, peripheral intravenous injection and in situ intrahepatic injection, as indicated by the increase in survival time and the decrease in liver injury [41]. Another study showed that transplantation via the hepatic artery was not beneficial for the transdifferentiation of MSCs.

Intravenous injection is the most popular route for clinical therapy because of its convenience. Is it the optimal method for cell transplantation? We must look for evidence from preclinical trials because there are no clinical trials comparing the effectiveness of intravenous injection and other routes. Animal studies have shown that cells transplanted via intravenous injection will accumulate in the lung. E. Eggenhofer demonstrated that in the first few hours, 60% of MSCs injected intravenously accumulated in the lungs and did not move to the liver afterward. These cells were probably cleared by immune cells [42]. Higashimoto et al. [43] showed that, after intravenous injection in mice with ConA induced hepatitis, GFP-labeled MSCs were found only in the lung but not in the liver. Cao et al. [44] determined that intraportal injection of MSCs restored hepatic function in ALF pigs, while transplantation of MSCs via the jugular vein did not. Li et al. [45] also administered MSCs via the peripheral vein and intraportal route into ALF pigs. They reported that the injection of MSCs via a peripheral vein did not rescue ALF pigs, while most of the ALF pigs survived for over 6 months after transplantation of MSCs via intraportal injection.

Intraportal injection is obviously the optimal route for MSC transplantation to treat liver diseases because of faster engraftment and the avoidance of off-target accumulation. In fact, we must evaluate the condition of patients and the potential risk of using a specific route before choosing the injection route. For instance, we need to know if there is thrombosis in the portal vein or technical issues. If there are difficulties involved in intraportal injection, intrasplenic injection or intravenous injection is probably a widely accepted alternative approach, and more MSCs are suggested to be prepared.

Doses used for MSC transplantation

The doses of MSCs applied in clinical therapy were not exact. It is very difficult to assess an optimal dosing strategy for MSC transplantation because most of the recent clinical trials were aimed at observing the efficiency of MSC therapy but did not determine the optimal dose. Even so, we can still provide some guidance based on these clinical trials. Most clinical trials apply MSCs according to the body weight of patients (n = 9, 0.5–3 × 106/kg as a single dose), while others apply MSCs according to the total quantity of cells (n = 7, 1–20 × 107). According to other medicine dosing strategies, injection according to body weight may be more reasonable. An Egypt study in 2013 involving transplanting MSCs into patients with liver cirrhosis showed that as few as 1 × 107 MSCs were effective for 6 months without any side effects [46]. In the same year, another study used MSCs in patients with liver cirrhosis and found that 2 × 108 MSCs showed no significant effect after 12 months compared with placebo [8]. However, there are other effective clinical trials that used more than 2 × 108 MSCs. It is important to bear in mind that we cannot draw a conclusion from different trials. There are other parameters involved in this process, such as the condition of patients, progression of diseases and treatment regimens. Among the recent clinical trials involving applying MSCs to treat liver diseases, the total number of MSCs used was from ~ 107−  ~ 109, regardless of which method was chosen to deliver the dose. The large range of doses used is hard to explain because there are few studies involving comparisons of different doses in the same clinical trial. However, we know that as few as 1 × 107 cells can be helpful.

Most completed clinical trials injected MSCs only once, and others injected MSCs multiple times, with up to 9 injections in one experiment [ClinicalTrials.gov NCT02223897]. How long would one dose of MSCs be effective? Is it necessary to inject MSCs several times? One study that used MSCs for liver cirrhosis treatment showed that MSCs could improve liver function over two years. No difference was observed between the control group and MSC group after two years [17]. As a result, the effect of one injection will not last that long. However, another clinical trial involving treatment for liver cirrhosis showed that there was no significant difference between the effect of one or two injections during a year [10]. This is probably because the second injection was performed only one month after the first injection. From these two studies, we can conclude that a longer interval for the second injection is probably beneficial for improving the therapeutic efficiency of MSCs.

Mechanism of MSC therapy for liver disease

In order to elucidate how MSCs play a positive role in the treatment of the above-mentioned liver diseases, we present the current findings regarding the molecular mechanism involved in the MSC-dependent modulation of liver diseases via a brief overview. A large number of studies have reported that MSC transplantation could promote partial recovery of liver function and alleviate liver inflammation in several animal models of liver fibrosis or cirrhosis. The mechanisms of the effects of MSCs on treating liver diseases have been evaluated from various perspectives in basic studies.

Immunomodulation capacity of MSCs

Most previous studies have shown that MSCs could improve or repair injured tissue by modulating tissue immune responses through direct cell-to-cell interaction or paracrine secretion. MSCs could modulate innate and adaptive immune responses.

The induction of CD4+CD25+FoxP3+ regulatory T cells (Tregs) is critical for MSC-mediated immunomodulation. Previous studies indicated that an imbalance in Treg/Th17 cells may be associated with liver diseases, such as autoimmune hepatitis, chronic hepatitis B, and alcoholic liver disease. A random trial reported that compared with those in the control group, the serum levels of interleukin-17 (IL-17), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) were significantly lower in the transplantation group. Furthermore, a significant increase in Tregs and a marked decrease in Th17 cells were observed in the transplantation group, indicating that BM-MSCs exhibit potent immunosuppressive and anti-inflammatory effects through the regulation of serum levels of inflammatory cytokines [6]. In line with the above study, Shi et al. [19] reported a pilot study using MSCs for treating liver transplant recipients. The data showed that after MSC infusion, Tregs in the liver were upregulated, whereas Th17 cells were downregulated. They also found that the percentage of HLA-DR+ CD4+ T cells was significantly decreased after UC-MSC infusions, which may facilitate the suppression of alloreactive responses. To date, only a few clinical protocols have included ex vivo immunologic studies to gain insight into the mechanistic effects of MSC therapy in liver disease. There is an increasingly large body of work that supports the immunoregulatory capacity of transferred MSCs in rodent models of liver disease. In nonclinical experiments, several different molecules secreted by MSCs have been reported to have an immunomodulatory effect on T cell activities, including inducible nitric oxide synthase (iNOS), hepatocyte growth factor (HGF), prostaglandin E2 (PGE2) and transforming growth factor (TGF)-β [47, 48]. Another study demonstrated that MSCs can secrete matrix metalloproteinases (MMPs), such as MMP-2 and MMP-9, that suppress T cell activation by cleaving surface CD25 molecules on T cells [49]. Furthermore, MSCs have also been shown to promote the generation and development of Tregs by secreting TGF-β. Of note, TGF-β is a two-edged sword in that it has immunosuppressive effects that alleviate liver inflammation [50] but can also promote the progression of liver fibrosis [51, 52].

In addition, MSCs are reported to exhibit immunomodulatory effects in macrophages, which play a central role in both fibrosis and fibrotic resolution in the liver. Watanabe et al. found that MSCs could change the polarity of macrophages toward an M2 anti-inflammatory phenotype, which involves the secretion of various anti-inflammatory factors, including chemokine ligand 1 (CCL-1) and IL-10, increases the production of matrix metalloproteinases to decrease ECM, and increases the phagocytosis of hepatocyte debris (during this process, macrophages increase the levels of pro-regenerative factors) [53]. Similar to the above study, murine adipose-derived MSCs were found to significantly increase the proportion of M2-like cells by increasing the production of IL-10 and arginase 1 activity [54]. In a mouse model of ischemia/reperfusion (IR)-induced sterile inflammatory injury of the liver, we found that adoptive transfer of MSCs reduced hepatocellular damage and shifted macrophage polarization from the M1 to M2 phenotype by increasing YAP and β-catenin nuclear translation in macrophages. Further research found that MSCs enhance the activity of the macrophage Hippo pathway, which in turn controls NLRP3 activation through a direct interaction between YAP and β-catenin and regulates XBP1-mediated NLRP3 activation, leading to reprogramming of macrophage polarization toward an anti-inflammatory M2 phenotype [55].

Direct and indirect effects of MSCs on the fate of activated HSCs

Inflammation and fibrosis have a very close relationship in liver disease. When the liver is damaged, quiescent hepatic stellate cells (HSCs) transdifferentiate into proliferative myofibroblastic/activated HSCs, which are the main contributors to liver fibrosis. Investigators have tried to determine the methods by which MSCs may influence the fate of myofibroblasts/activated HSCs. Reported hypotheses include a direct effect by cell–cell contact and MSC-secreted cytokines/growth factors or an indirect effect by cellular mediators, such as macrophages or even hepatocytes. Regarding the indirect effects, MSCs can regulate the activities of HSCs by modulating immune cell activity. For example, MSCs can induce changes in the cytokine profile of activated macrophages by increasing the production of IL-10, PGE2 and matrix metalloproteinases and thereby promote the resolution of fibrosis [56]. On the other hand, MSCs can degrade ECM directly by secreting matrix metalloproteinases, such as MMP-13 and MMP-9 [57]. In vitro experiments have also demonstrated that after coculture with MSCs, the proliferation and activation of HSCs was inhibited by ADSCs, and the apoptosis of HSCs was promoted [58, 59]. Furthermore, a recent study reported that tumor necrosis factor-inducible gene 6 protein (TSG-6), a cytokine released from MSCs, could suppress HSC activation and induce the expression of stem cell markers in these cells. Then, the stem cell-like cells derived from HSCs treated with TSG-6 can form organoids that contribute to liver regeneration [60]. The milk fat globule-EGF factor 8 (MFGE8) was identified by Su et al. [61] as a novel key antifibrotic factor based on its role in the modulation of TGF-β signaling. In an in vivo analysis of mice, hUC-MSC secretomes were injected into mice with fibrosis, which led to a significant inhibition of liver fibrosis. MFGE8 is an antifibrotic protein in MSC secretomes that strongly inhibits TGF-β signaling and reduces extracellular matrix deposition and liver fibrosis in mice [62].

Differentiation of MSCs into Hepatocyte-like Cells

A majority of in vitro studies demonstrated that MSCs had the capacity to differentiate into hepatocyte-like cells with liver-specific morphology and function with the help of specific growth factors, such as HGF, EGF, FGF, and OSM [63,64,65,66]. Furthermore, Yan et al. [67] showed that by mimicking the microenvironment of liver fibrosis using 50 g/L rat fibrotic liver tissue extracts, hUC-MSCs were stimulated to differentiate into hepatocyte-like cells in a shorter period of time. Similar results have been confirmed by in vivo experiments. Interestingly, Park et al. [68] previously transplanted human MSCs into rats with a fibrotic liver. Then, 21 days after transplantation, human albumin-positive cells were detected in the MSC infusion group, which suggested that the transplanted MSCs could differentiate into albumin-secreting hepatocyte-like cells in the damaged livers of the rats. In line with these findings, Zhang et al. [69] reported that the expression of human ALB, AFP, CK18 and CK19 were detected in the liver tissue of fibrotic and cirrhotic rats after hUC-MSC transplantation, suggesting that transplanted hUC-MSCs could migrate into the injured liver, where they could differentiate into hepatocyte-like cells. Furthermore, they also demonstrated that hUC-MSCs did not directly differentiate into functional hepatocytes; they first differentiated into epithelial cell-like cells and subsequently differentiated into hepatocyte-like cells. All the above findings indicated that MSCs could differentiate into hepatocyte-like cells through exposure to the liver fibrosis microenvironment both in vitro and in vivo. However, there are also many research reports that indicate that the trans-differentiation of MSCs into hepatocytes has rarely been observed (less than 1% of the total liver mass) in animal models after MSC infusion [70]. Similarly, menstrual blood-derived stem cells were demonstrated to improve liver function by eliminating collagen deposition and inhibiting proliferative HSCs via paracrine mediators, but few of the transplanted cells were found to differentiate into functional hepatocyte-like cells [71]. Based on the above studies, MSCs are believed to exhibit a positive treatment effect in two ways: directly by cell differentiation and indirectly by paracrine effects. Many studies have attempted to use exosomes or culture supernatants of MSCs to achieve therapeutic effects [72,73,74], indicating that the success of MSC therapy does not completely correlate with the efficiency of cell engraftment and replacement. For treatment, it is likely that the paracrine effects of MSCs play a more vital role. Furthermore, we believe that in some cases, alternative treatments, such as MSC exosomes or MSC culture supernatant therapy, may be more effective than treatment with MSCs themselves, as MSCs have robust plasticity, differentiation characteristics and immunomodulatory properties. Infusion of MSCs in different microenvironmental conditions may change their immunoregulatory characteristics, thereby affecting the stability of their therapeutic effects.

In conclusion, the treatment mechanisms mentioned above do not necessarily appear in the process of treating the same disease at the same time. According to the basic characteristics of different liver diseases, the role of MSCs in the treatment process may be focusing effect. For example, in applying for treatment inflammation related liver disease, such as hepatitis induced cirrhosis or complications of liver transplantation, the immunomodulatory function of MSCs may play a more vital role. However, for liver cirrhosis, the effects of MSCs on the fate of activated HSCs may also take part in the treatment process. In another hand, the efficacy of MSCs treatment in liver failure may mainly depend on its property of differentiation into hepatocyte-like cells.

Modification of MSCs for therapy

Conventional unmanipulated MSCs have been the mainstay of therapeutic studies, and more efforts need to be made to enhance their efficacy. In fact, priming of MSCs before use is intended to enhance their biological properties and function in some animal models. This may involve the combination of MSCs with other factors, pretreatment and genetic modification of MSCs, and the use of secretomes of MSCs.

Pretreatment of MSCs

Pretreatment of MSCs may improve their potential to treat liver diseases by increasing their homing, differentiation and immunoregulation capacity. Pretreatment of MSCs with zeaxanthin dipalmitate (ZD) could increase the cell survival rate and enhance the capacity of MSCs to differentiate into hepatocytes. In addition, ZD-pretreated MSCs ameliorated liver injury to a great extent [75]. The anti-inflammatory property of MSCs could be modulated by the inflammatory microenvironment. Thus, pretreatment with inflammatory factors such as TNF-α combined with IFN-γ may promote the anti-inflammatory ability of MSCs and shorten the functioning time in vivo [76]. However, the anti-inflammatory effect of MSCs is probably repressed after differentiation. Should we enhance the differentiation ability or immune regulation ability of MSCs by priming? This may depend on the specific disease type. In addition to MSC priming, the pretreatment of MSC recipients also exerted a similar effect in vivo. Pretreatment of recipients with both anti-PMN [77] and IL-1β siRNA [78] could promote the therapeutic efficacy of MSCs. Dexamethasone has been demonstrated to repress the repair capacity of MSCs [79]. Thus, dexamethasone should be withdrawn before MSC administration.

Genetic modification of MSCs

In addition to MSC pretreatment, genetic modification of MSCs may be another powerful approach for disease therapy. To date, there have been many genetic modifications targeting MSC therapy in animal models. Both c-Met [80] and CXCR4 [81] overexpression could enhance the migration and engraftment of MSCs into injured sites and thus promote liver injury repair. In addition to showing the enhancement of homing, IGF-1-modified MSCs were found to have an enhanced anti-fibrotic ability compared to normal MSCs [82]. In fact, a large proportion of gene modifications of MSCs have been applied in liver cancer treatment. MSCs can deliver cytokines, such as IFN-β [83, 84], IFN-α2b [85], tumor necrosis factor-related apoptosis inducing ligand (TRAIL) [86, 87] and IL-12 [88], to inhibit hepatocarcinogenesis. MSCs also deliver the immune effector molecule CD3scfv to stimulate antitumor immunity [89]. In addition, MSCs can deliver the suicide gene HSV-Tk to induce cytotoxicity in hepatoma cells [90]. Overall, MSC-delivered cytokines could be more stable and longer lasting than pure cytokines and produce reduced side effects. Moreover, the use of genetically modified MSCs would be more safe than transfecting viruses directly into the body. However, considering the potential of MSCs to promote tumor growth, a safety evaluation should be carried out strictly before clinical application.

Cell-free therapy with MSCs

The status of transplanted cells in vivo and the potential tumorigenic risks of MSCs have raised concerns about their effectiveness and safety. MSCs have been shown to exert their anti-inflammatory and tissue repair functions through the paracrine effects of cytokines and other secretomes. As a result, increasing evidence has confirmed the efficacy of conditioned medium (CM) and exosomes of MSCs in animal models of liver disease. MSC-CM exerts anti-inflammatory functions via production of anti-inflammatory cytokines, such as IL-10, IL-13, and IL-27 [91], and contributes to the expansion of immune-suppressive T cells (Tregs) [92]. MSC-CM also restored liver function by promoting hepatocyte proliferation and inhibiting hepatocyte apoptosis through HGF and VEGF secretion [93]. Moreover, Li et al. [72] found that UC-MSC-derived exosomes inhibited liver fibrosis by repressing EMT of hepatocytes and collagen production in a mouse model. Exosomes also inactivate the TGF-β1/Smad signaling pathway, which is involved in fibrogenesis. On the other hand, miRNAs in exosomes contribute to inhibiting fibrosis formation [94]. Thus, the use of the MSC secretome as an acellular therapeutic agent could provide several advantages over the use of cell-based therapies for liver diseases.

Prospective of clinical application of MSCs

MSC therapy has been generally regarded as a safe and promising therapeutic strategy in clinical trials for patients with liver disease, including complications due to liver transplantation, liver failure, cirrhosis due to alcohol, HBV, or HCV, and primary biliary cholangitis. However, the application of MSCs for the treatment of related diseases has not been approved by official agencies such as the FDA, and this therapeutic strategy has not been as popular as expected. We speculate that this is probably because there are still some vital problems that have not been solved in the application of MSC therapy (Fig. 4). In addition, the inconsistency and ambiguity of MSCs as a type of stem cells may be one of the main reasons for the limited application of MSCs. The creator of the term "MSC", Arnold Caplan, recommended using "Medicinal Signaling Cells" instead of "Mesenchymal stem cells" to best describe these cells [95]. MSCs have been found as stem cells at first because of their self-renewal and multi-differentiation. However, their application will be greatly limited if we treat MSCs only as stem cells. MSCs also have some properties beyond stemness, such as migrating to injury sites and immunoregulation. These properties are important for liver disease therapy. Balancing different views of using MSCs as stem cells or other cell type will improve application of MSCs in liver disease therapy.

Fig. 4
figure 4

Concerns of MSC therapy for liver disease from bench to bedside

Full size image

First, it is important to maintain the quality and stability of MSCs used for disease therapy. Based on the clinical trials mentioned above, there is no uniform standard for evaluating the quality of MSCs in each trial. The characteristics of MSCs from autologous bone marrow from different patients are likely to be quite different due to the diversity of factors such as patient age, gender, disease status, and other factors. For instance, a researcher in Brazil reported that MSCs isolated from multiple sclerosis patients have distinct gene expression profiles and functional defects implicated in MSC immunomodulatory and immunosuppressive activity compared with those from their healthy counterparts [96]. Another group also demonstrated that MSCs derived from hepatitis B patients proliferated slowly and tended to undergo senescence [97]. Therefore, we believe that the establishment of a complete MSC quality standard evaluation system is needed. Based on such a standard, we can know which MSCs from autologous patients are qualified or meet the standards and which should be eliminated and replaced with allogenic MSCs for treatment.

For the treatment of disease, the optimal dose of MSCs and the number of infusions is not well defined. To date, a very few articles have examined how many doses of MSCs could produce the best effect and whether transplanting more MSCs results in a better treatment effect. Therefore, we also have no idea what the optimal number of injections and interval times would be. By integrating data from the different clinical trials mentioned above, we believe that MSCs should be effective when the number of administered MSCs is within a certain range. Freshly isolated MSCs showed better homing than cultured cells [98]. Thus, the most suitable dose should be determined based on balancing the corresponding therapeutic effect and the time and economic costs required to obtain the corresponding dose of MSCs. Furthermore, as we mentioned in the third part of the review, it is not effective to perform multiple repeated MSC injections in a short period of time, such as within 6 months. In conclusion, low doses and multiple injections with longer intervals are probably the most effective and economical strategy for MSC application.

Judging from the large number of in vivo studies of MSCs, regardless of whether MSCs were obtained from autologous or allogenic sources or from bone marrow, umbilical cord or fat, MSC therapy did not cause serious adverse reactions, tumor formation or transplant-related deaths in clinical trials. Thus, the source of MSCs that should be used depends on the specific situation. For instance, allogeneic MSCs, compared with autologous MSCs, have more potential advantages for the treatment of ACLF. Because a characteristic of ACLF is its rapid progression, the use of allogeneic MSCs may be preferred because of their immediate availability, while it always needs to take longer time for culturing autologous MSCs to obtain a sufficient quantity.

Of note, another central issue for the future success of cell transplantation is the ability to noninvasively assess the fate, migration patterns, and survival of transplanted cells. If we can track the fate of the transplanted MSCs, we could know the proportion of cells that home in and engraft in the liver and the way that cells exert their therapeutic effects. The classic method of MSCs labelling uses retroviral vectors to express fluorescent protein or gene-modified animal models to track MSCs in vivo [99, 100]. However, the visualization of cells that home in in different organs requires sacrificing of the animal, as the tissue penetrability of fluorescence is limited. Therefore, these technologies are not suitable for clinical applications. More noninvasive techniques have been employed constantly. Endomicroscopy was reported as a clinically available noninvasive cellular tracking method used to track cell fate in vivo [101]. Furthermore, cellular magnetic resonance imaging (MRI) using fluorine- or iron-based nanoemulsions is also regarded as a great means to detect transplanted cells in vivo because of its high specificity and precise quantification [102, 103]. However, the potential limitations of these tracking tools are the possibility of transferring the label to local bystander cells and the effect of the label on MSC basic feature. More advanced and improved technology for transplanted cell tracking needs to be employed.

Conclusions

According to clinical trials, MSC therapy has been regarded as a safe and promising therapeutic strategy for patients with end-stage liver disease, including liver cirrhosis, liver failure, and complications after liver transplantation. However, for MSCs to become a routine treatment for these liver diseases and to be widely used, further studies with larger samples and double-blind controlled trials are needed to increase the safety and efficacy of MSCs in the clinic. Furthermore, studies on the optimal MSC transplantation route, minimum effective number of MSCs, and tracking of MSCs are needed to provide more references and guidance for specific future clinical treatment programs. In addition to the use of conventional unmanipulated MSCs, derived MSC therapies, such as the use of primed MSCs or gene-modified MSCs or cell-free therapy, may be promising and practical treatments in the future.

Availability of data and materials

Not applicable.

Abbreviations

MSCs:

Mesenchymal stem cells

LC:

Liver cirrhosis

MELD score:

Model for end-stage liver disease scores

ACLF:

Acute-on-chronic liver failure

GCSF:

Granulocyte colony stimulating factor

BM:

Bone marrow

ALF:

Acute liver failure

UC:

Umbilical cord

AD:

Adipose tissue

IL-17:

Interleukin-17

TNF-α:

Tumor necrosis factor-α

IL-6:

Interleukin-6

iNOS:

Inducible nitric oxide synthase

HGF:

Hepatocyte growth factor

PGE2:

Prostaglandin E2

TGF:

Transforming growth factor

MMPs:

Matrix metalloproteinases

CCL-1:

Chemokine ligand 1

IR:

Ischemia/reperfusion

HSCs:

Hepatic stellate cells

TSG-6:

Tumor necrosis factor-inducible gene 6 protein

MFGE8:

Milk fat globule-EGF factor 8

ZD:

Zeaxanthin dipalmitate

TRAIL:

Tumor necrosis factor-related apoptosis inducing ligand

CM:

Conditioned medium

References

  1. Neuberger J. Liver transplantation in the United Kingdom. Liver Transpl. 2016;22(8):1129–35.

    Article  Google Scholar 

  2. Zhang Z, Wang FS. Stem cell therapies for liver failure and cirrhosis. J Hepatol. 2013;59(1):183–5.

    Article  Google Scholar 

  3. Zhu W, Shi XL, Xiao JQ, Gu GX, Ding YT, Ma ZL. Effects of xenogeneic adipose-derived stem cell transplantation on acute-on-chronic liver failure. HBPD Int. 2013;12(1):60–7.

    CAS  Google Scholar 

  4. Zhang Z, Lin H, Shi M, Xu R, Fu J, Lv J, et al. Human umbilical cord mesenchymal stem cells improve liver function and ascites in decompensated liver cirrhosis patients. J Gastroenterol Hepatol. 2012;27(Suppl 2):112–20.

    CAS  Article  Google Scholar 

  5. El-Ansary M, Abdel-Aziz I, Mogawer S, Abdel-Hamid S, Hammam O, Teaema S, et al. Phase II trial: undifferentiated versus differentiated autologous mesenchymal stem cells transplantation in Egyptian patients with HCV induced liver cirrhosis. Stem Cell Rev Reports. 2012;8(3):972–81.

    CAS  Article  Google Scholar 

  6. Xu L, Gong Y, Wang B, Shi K, Hou Y, Wang L, et al. Randomized trial of autologous bone marrow mesenchymal stem cells transplantation for hepatitis B virus cirrhosis: regulation of Treg/Th17 cells. J Gastroenterol Hepatol. 2014;29(8):1620–8.

    CAS  Article  Google Scholar 

  7. Fang X, Liu L, Dong J, Zhang J, Song H, Song Y, et al. A study about immunomodulatory effect and efficacy and prognosis of human umbilical cord mesenchymal stem cells in patients with chronic hepatitis B-induced decompensated liver cirrhosis. J Gastroenterol Hepatol. 2018;33(4):774–80.

    CAS  Article  Google Scholar 

  8. Mohamadnejad M, Alimoghaddam K, Bagheri M, Ashrafi M, Abdollahzadeh L, Akhlaghpoor S, et al. Randomized placebo-controlled trial of mesenchymal stem cell transplantation in decompensated cirrhosis. Liver Int. 2013;33(10):1490–6.

    CAS  Article  Google Scholar 

  9. Kharaziha P, Hellstrom PM, Noorinayer B, Farzaneh F, Aghajani K, Jafari F, et al. Improvement of liver function in liver cirrhosis patients after autologous mesenchymal stem cell injection: a phase I–II clinical trial. Eur J Gastroenterol Hepatol. 2009;21(10):1199–205.

    CAS  Article  Google Scholar 

  10. Suk KT, Yoon JH, Kim MY, Kim CW, Kim JK, Park H, et al. Transplantation with autologous bone marrow-derived mesenchymal stem cells for alcoholic cirrhosis: phase 2 trial. Hepatology. 2016;64(6):2185–97.

    CAS  Article  Google Scholar 

  11. Liang J, Zhang H, Zhao C, Wang D, Ma X, Zhao S, et al. Effects of allogeneic mesenchymal stem cell transplantation in the treatment of liver cirrhosis caused by autoimmune diseases. Int J Rheumatic Dis. 2017;20(9):1219–26.

    CAS  Article  Google Scholar 

  12. Wang L, Li J, Liu H, Li Y, Fu J, Sun Y, et al. Pilot study of umbilical cord-derived mesenchymal stem cell transfusion in patients with primary biliary cirrhosis. J Gastroenterol Hepatol. 2013;28(Suppl 1):85–92.

    CAS  Article  Google Scholar 

  13. Gaude GS, Chaudhury A, Hattiholi J. Drug-induced hepatitis and the risk factors for liver injury in pulmonary tuberculosis patients. J Family Med Primary Care. 2015;4(2):238–43.

    Article  Google Scholar 

  14. Peng L, Xie DY, Lin BL, Liu J, Zhu HP, Xie C, et al. Autologous bone marrow mesenchymal stem cell transplantation in liver failure patients caused by hepatitis B: short-term and long-term outcomes. Hepatology. 2011;54(3):820–8.

    Article  Google Scholar 

  15. Shi M, Zhang Z, Xu R, Lin H, Fu J, Zou Z, et al. Human mesenchymal stem cell transfusion is safe and improves liver function in acute-on-chronic liver failure patients. Stem Cells Transl Med. 2012;1(10):725–31.

    CAS  Article  Google Scholar 

  16. Lin BL, Chen JF, Qiu WH, Wang KW, Xie DY, Chen XY, et al. Allogeneic bone marrow-derived mesenchymal stromal cells for hepatitis B virus-related acute-on-chronic liver failure: a randomized controlled trial. Hepatology. 2017;66(1):209–19.

    CAS  Article  Google Scholar 

  17. Amer ME, El-Sayed SZ, El-Kheir WA, Gabr H, Gomaa AA, El-Noomani N, et al. Clinical and laboratory evaluation of patients with end-stage liver cell failure injected with bone marrow-derived hepatocyte-like cells. Eur J Gastroenterol Hepatol. 2011;23(10):936–41.

    Article  Google Scholar 

  18. Salama H, Zekri AR, Medhat E, Al Alim SA, Ahmed OS, Bahnassy AA, et al. Peripheral vein infusion of autologous mesenchymal stem cells in Egyptian HCV-positive patients with end-stage liver disease. Stem Cell Res Therapy. 2014;5(3):70.

    Article  Google Scholar 

  19. Shi M, Liu Z, Wang Y, Xu R, Sun Y, Zhang M, et al. A pilot study of mesenchymal stem cell therapy for acute liver allograft rejection. Stem Cells Transl Med. 2017;6(12):2053–61.

    CAS  Article  Google Scholar 

  20. Detry O, Vandermeulen M, Delbouille MH, Somja J, Bletard N, Briquet A, et al. Infusion of mesenchymal stromal cells after deceased liver transplantation: a phase I–II, open-label, clinical study. J Hepatol. 2017;67(1):47–55.

    Article  Google Scholar 

  21. Friedenstein AJ, Chailakhjan RK, Lalykina KS. The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells. Cell Tissue Kinetics. 1970;3(4):393–403.

    CAS  Google Scholar 

  22. Seki A, Sakai Y, Komura T, Nasti A, Yoshida K, Higashimoto M, et al. Adipose tissue-derived stem cells as a regenerative therapy for a mouse steatohepatitis-induced cirrhosis model. Hepatology. 2013;58(3):1133–42.

    CAS  Article  Google Scholar 

  23. Tsai PC, Fu TW, Chen YM, Ko TL, Chen TH, Shih YH, et al. The therapeutic potential of human umbilical mesenchymal stem cells from Wharton’s jelly in the treatment of rat liver fibrosis. Liver Transpl. 2009;15(5):484–95.

    Article  Google Scholar 

  24. Erices A, Conget P, Minguell JJ. Mesenchymal progenitor cells in human umbilical cord blood. Br J Haematol. 2000;109(1):235–42.

    CAS  Article  Google Scholar 

  25. Anker PS, Scherjon SA, Kleijburg-van C, de Groot-Swings GM, Claas FH, Fibbe WE, et al. Isolation of mesenchymal stem cells of fetal or maternal origin from human placenta. Stem Cells. 2004;22(7):1338–45.

    Article  Google Scholar 

  26. Anker PS, Scherjon SA, Kleijburg-van C, Noort WA, Claas FH, Willemze R, et al. Amniotic fluid as a novel source of mesenchymal stem cells for therapeutic transplantation. Blood. 2003;102(4):1548–9.

    Article  Google Scholar 

  27. Yan K, Zhang R, Chen L, Chen F, Liu Y, Peng L, et al. Nitric oxide-mediated immunosuppressive effect of human amniotic membrane-derived mesenchymal stem cells on the viability and migration of microglia. Brain Res. 2014;1590:1–9.

    CAS  Article  Google Scholar 

  28. Lei M, Li K, Li B, Gao LN, Chen FM, Jin Y. Mesenchymal stem cell characteristics of dental pulp and periodontal ligament stem cells after in vivo transplantation. Biomaterials. 2014;35(24):6332–43.

    CAS  Article  Google Scholar 

  29. Ogata Y, Mabuchi Y, Yoshida M, Suto EG, Suzuki N, Muneta T, et al. Purified human synovium mesenchymal stem cells as a good resource for cartilage regeneration. PLoS ONE. 2015;10(6):e0129096.

    Article  CAS  Google Scholar 

  30. Anker PS, Noort WA, Scherjon SA, Kleijburg-van C, Kruisselbrink AB, van Bezooijen RL, et al. Mesenchymal stem cells in human second-trimester bone marrow, liver, lung, and spleen exhibit a similar immunophenotype but a heterogeneous multilineage differentiation potential. Haematologica. 2003;88(8):845–52.

    Google Scholar 

  31. Gressner AM, Weiskirchen R, Breitkopf K, Dooley S. Roles of TGF-beta in hepatic fibrosis. Front Biosci. 2002;7:d793-807.

    CAS  Article  Google Scholar 

  32. Williams JT, Southerland SS, Souza J, Calcutt AF, Cartledge RG. Cells isolated from adult human skeletal muscle capable of differentiating into multiple mesodermal phenotypes. Am Surg. 1999;65(1):22–6.

    CAS  Google Scholar 

  33. Ohyama M, Zheng Y, Paus R, Stenn KS. The mesenchymal component of hair follicle neogenesis: background, methods and molecular characterization. Exp Dermatol. 2010;19(2):89–99.

    Article  Google Scholar 

  34. Batsali AK, Kastrinaki MC, Papadaki HA, Pontikoglou C. Mesenchymal stem cells derived from Wharton’s Jelly of the umbilical cord: biological properties and emerging clinical applications. Curr Stem Cell Res Ther. 2013;8(2):144–55.

    CAS  Article  Google Scholar 

  35. Mueller SM, Glowacki J. Age-related decline in the osteogenic potential of human bone marrow cells cultured in three-dimensional collagen sponges. J Cell Biochem. 2001;82(4):583–90.

    CAS  Article  Google Scholar 

  36. Lu LL, Liu YJ, Yang SG, Zhao QJ, Wang X, Gong W, et al. Isolation and characterization of human umbilical cord mesenchymal stem cells with hematopoiesis-supportive function and other potentials. Haematologica. 2006;91(8):1017–26.

    CAS  Google Scholar 

  37. Hsieh JY, Fu YS, Chang SJ, Tsuang YH, Wang HW. Functional module analysis reveals differential osteogenic and stemness potentials in human mesenchymal stem cells from bone marrow and Wharton’s jelly of umbilical cord. Stem Cells Dev. 2010;19(12):1895–910.

    CAS  Article  Google Scholar 

  38. Cho PS, Messina DJ, Hirsh EL, Chi N, Goldman SN, Lo DP, et al. Immunogenicity of umbilical cord tissue derived cells. Blood. 2008;111(1):430–8.

    CAS  Article  Google Scholar 

  39. Deuse T, Stubbendorff M, Tang-Quan K, Phillips N, Kay MA, Eiermann T, et al. Immunogenicity and immunomodulatory properties of umbilical cord lining mesenchymal stem cells. Cell Transplant. 2011;20(5):655–67.

    Article  Google Scholar 

  40. Strioga M, Viswanathan S, Darinskas A, Slaby O, Michalek J. Same or not the same? Comparison of adipose tissue-derived versus bone marrow-derived mesenchymal stem and stromal cells. Stem Cells Dev. 2012;21(14):2724–52.

    CAS  Article  Google Scholar 

  41. Sang JF, Shi XL, Han B, Huang T, Huang X, Ren HZ, et al. Intraportal mesenchymal stem cell transplantation prevents acute liver failure through promoting cell proliferation and inhibiting apoptosis. HBPD Int. 2016;15(6):602–11.

    Google Scholar 

  42. Eggenhofer E, Benseler V, Kroemer A, Popp FC, Geissler EK, Schlitt HJ, et al. Mesenchymal stem cells are short-lived and do not migrate beyond the lungs after intravenous infusion. Front Immunol. 2012;3:297.

    CAS  Article  Google Scholar 

  43. Higashimoto M, Sakai Y, Takamura M, Usui S, Nasti A, Yoshida K, et al. Adipose tissue derived stromal stem cell therapy in murine ConA-derived hepatitis is dependent on myeloid-lineage and CD4+ T-cell suppression. Eur J Immunol. 2013;43(11):2956–68.

    CAS  Article  Google Scholar 

  44. Cao H, Yang J, Yu J, Pan Q, Li J, Zhou P, et al. Therapeutic potential of transplanted placental mesenchymal stem cells in treating Chinese miniature pigs with acute liver failure. BMC Med. 2012;10:56.

    CAS  Article  Google Scholar 

  45. Wei T, Lv Y. Immediate intraportal transplantation of human bone marrow mesenchymal stem cells prevents death from fulminant hepatic failure in pigs. Hepatology. 2013;58(1):451–2.

    Article  Google Scholar 

  46. Amin MA, Sabry D, Rashed LA, Aref WM, el-Ghobary MA, Farhan MS, et al. Short-term evaluation of autologous transplantation of bone marrow-derived mesenchymal stem cells in patients with cirrhosis: Egyptian study. Clin Transplant. 2013;27(4):607–12.

    Article  Google Scholar 

  47. Meisel R, Zibert A, Laryea M, Gobel U, Daubener W, Dilloo D. Human bone marrow stromal cells inhibit allogeneic T-cell responses by indoleamine 2,3-dioxygenase-mediated tryptophan degradation. Blood. 2004;103(12):4619–21.

    CAS  Article  Google Scholar 

  48. Zafranskaya M, Nizheharodava D, Yurkevich M, Ivanchik G, Demidchik Y, Kozhukh H, et al. PGE2 contributes to in vitro MSC-mediated inhibition of non-specific and antigen-specific T cell proliferation in MS patients. Scand J Immunol. 2013;78(5):455–62.

    CAS  Article  Google Scholar 

  49. Ding Y, Xu D, Feng G, Bushell A, Muschel RJ, Wood KJ. Mesenchymal stem cells prevent the rejection of fully allogenic islet grafts by the immunosuppressive activity of matrix metalloproteinase-2 and -9. Diabetes. 2009;58(8):1797–806.

    CAS  Article  Google Scholar 

  50. Zhang Y, Cai W, Huang Q, Gu Y, Shi Y, Huang J, et al. Mesenchymal stem cells alleviate bacteria-induced liver injury in mice by inducing regulatory dendritic cells. Hepatology. 2014;59(2):671–82.

    CAS  Article  Google Scholar 

  51. Li J, Wang Y, Ma M, Jiang S, Zhang X, Zhang Y, et al. Autocrine CTHRC1 activates hepatic stellate cells and promotes liver fibrosis by activating TGF-beta signaling. EBioMedicine. 2019;40:43–55.

    Article  Google Scholar 

  52. Wu N, Meng F, Invernizzi P, Bernuzzi F, Venter J, Standeford H, et al. The secretin/secretin receptor axis modulates liver fibrosis through changes in transforming growth factor-beta1 biliary secretion in mice. Hepatology. 2016;64(3):865–79.

    CAS  Article  Google Scholar 

  53. Watanabe Y, Tsuchiya A, Seino S, Kawata Y, Kojima Y, Ikarashi S, et al. Mesenchymal stem cells and induced bone marrow-derived macrophages synergistically improve liver fibrosis in mice. Stem Cells Translat Med. 2019;8(3):271–84.

    CAS  Article  Google Scholar 

  54. Anderson P, Souza-Moreira L, Morell M, Caro M, O’Valle F, Gonzalez-Rey E, et al. Adipose-derived mesenchymal stromal cells induce immunomodulatory macrophages which protect from experimental colitis and sepsis. Gut. 2013;62(8):1131–41.

    CAS  Article  Google Scholar 

  55. Li C, Jin Y, Wei S, Sun Y, Jiang L, Zhu Q, et al. Hippo signaling controls NLR family pyrin domain containing 3 activation and governs immunoregulation of mesenchymal stem cells in mouse liver injury. Hepatology. 2019;70(5):1714–31.

    CAS  Article  Google Scholar 

  56. Maggini J, Mirkin G, Bognanni I, Holmberg J, Piazzon IM, Nepomnaschy I, et al. Mouse bone marrow-derived mesenchymal stromal cells turn activated macrophages into a regulatory-like profile. PLoS ONE. 2010;5(2):e9252.

    Article  CAS  Google Scholar 

  57. Higashiyama R, Inagaki Y, Hong YY, Kushida M, Nakao S, Niioka M, et al. Bone marrow-derived cells express matrix metalloproteinases and contribute to regression of liver fibrosis in mice. Hepatology. 2007;45(1):213–22.

    CAS  Article  Google Scholar 

  58. Chen S, Xu L, Lin N, Pan W, Hu K, Xu R. Activation of Notch1 signaling by marrow-derived mesenchymal stem cells through cell-cell contact inhibits proliferation of hepatic stellate cells. Life Sci. 2011;89(25–26):975–81.

    CAS  Article  Google Scholar 

  59. Yu F, Ji S, Su L, Wan L, Zhang S, Dai C, et al. Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo. J Formosan Med Assoc Taiwan yi zhi. 2015;114(2):130–8.

    CAS  Article  Google Scholar 

  60. Wang S, Kim J, Lee C, Oh D, Han J, Kim TJ, et al. Tumor necrosis factor-inducible gene 6 reprograms hepatic stellate cells into stem-like cells, which ameliorates liver damage in mouse. Biomaterials. 2019;219:119375.

    CAS  Article  Google Scholar 

  61. Raymond A, Ensslin MA, Shur BD. SED1/MFG-E8: a bi-motif protein that orchestrates diverse cellular interactions. J Cell Biochem. 2009;106(6):957–66.

    CAS  Article  Google Scholar 

  62. An SY, Jang YJ, Lim HJ, Han J, Lee J, Lee G, et al. Milk fat globule-EGF factor 8, secreted by mesenchymal stem cells, protects against liver fibrosis in mice. Gastroenterology. 2017;152(5):1174–86.

    CAS  Article  Google Scholar 

  63. Alizadeh E, Eslaminejad MB, Akbarzadeh A, Sadeghi Z, Abasi M, Herizchi R, et al. Upregulation of MiR-122 via Trichostatin A treatments in hepatocyte-like cells derived from mesenchymal stem cells. Chem Biol Drug Des. 2016;87(2):296–305.

    CAS  Article  Google Scholar 

  64. Xu F, Liu J, Deng J, Chen X, Wang Y, Xu P, et al. Rapid and high-efficiency generation of mature functional hepatocyte-like cells from adipose-derived stem cells by a three-step protocol. Stem cell Res Therapy. 2015;6:193.

    Article  CAS  Google Scholar 

  65. Zhao Q, Ren H, Li X, Chen Z, Zhang X, Gong W, et al. Differentiation of human umbilical cord mesenchymal stromal cells into low immunogenic hepatocyte-like cells. Cytotherapy. 2009;11(4):414–26.

    CAS  Article  Google Scholar 

  66. An SY, Han J, Lim HJ, Park SY, Kim JH, Do BR, et al. Valproic acid promotes differentiation of hepatocyte-like cells from whole human umbilical cord-derived mesenchymal stem cells. Tissue Cell. 2014;46(2):127–35.

    CAS  Article  Google Scholar 

  67. Yan C, Xue G, Wu L, Liu J, Hou Y. Differentiation of human umbilical cord mesenchymal stem cells into hepatocytes induced by rat fibrotic liver tissue extracts. Zhongguo xiu fu chong jian wai ke za zhi. 2015;29(7):878–83.

    Google Scholar 

  68. Lin SZ, Chang YJ, Liu JW, Chang LF, Sun LY, Li YS, et al. Transplantation of human Wharton’s Jelly-derived stem cells alleviates chemically induced liver fibrosis in rats. Cell Transplant. 2010;19(11):1451–63.

    Article  Google Scholar 

  69. Zhang GZ, Sun HC, Zheng LB, Guo JB, Zhang XL. In vivo hepatic differentiation potential of human umbilical cord-derived mesenchymal stem cells: therapeutic effect on liver fibrosis/cirrhosis. World J Gastroenterol. 2017;23(46):8152–68.

    CAS  Article  Google Scholar 

  70. Dai LJ, Li HY, Guan LX, Ritchie G, Zhou JX. The therapeutic potential of bone marrow-derived mesenchymal stem cells on hepatic cirrhosis. Stem cell research. 2009;2(1):16–25.

    Article  Google Scholar 

  71. Chen L, Zhang C, Chen L, Wang X, Xiang B, Wu X, et al. Human menstrual blood-derived stem cells ameliorate liver fibrosis in mice by targeting hepatic stellate cells via paracrine mediators. Stem cells translational medicine. 2017;6(1):272–84.

    CAS  Article  Google Scholar 

  72. Li T, Yan Y, Wang B, Qian H, Zhang X, Shen L, et al. Exosomes derived from human umbilical cord mesenchymal stem cells alleviate liver fibrosis. Stem Cells Devel. 2013;22(6):845–54.

    CAS  Article  Google Scholar 

  73. Shao M, Xu Q, Wu Z, Chen Y, Shu Y, Cao X, et al. Exosomes derived from human umbilical cord mesenchymal stem cells ameliorate IL-6-induced acute liver injury through miR-455-3p. Stem Cell Res Therapy. 2020;11(1):37.

    CAS  Article  Google Scholar 

  74. Tan CY, Lai RC, Wong W, Dan YY, Lim SK, Ho HK. Mesenchymal stem cell-derived exosomes promote hepatic regeneration in drug-induced liver injury models. Stem Cell Res Therapy. 2014;5(3):76.

    Article  CAS  Google Scholar 

  75. Liu Y, Xiong Y, Xing F, Gao H, Wang X, He L, et al. Precise regulation of miR-210 is critical for the cellular homeostasis maintenance and transplantation efficacy enhancement of mesenchymal stem cells in acute liver failure therapy. Cell. 2017;26(5):805–20.

    Article  Google Scholar 

  76. Linero I, Chaparro O. Paracrine effect of mesenchymal stem cells derived from human adipose tissue in bone regeneration. PLoS ONE. 2014;9(9):e107001.

    Article  CAS  Google Scholar 

  77. Zhao X, Shi X, Zhang Z, Ma H, Yuan X, Ding Y. Combined treatment with MSC transplantation and neutrophil depletion ameliorates D-GalN/LPS-induced acute liver failure in rats. Clin Res Hepatol Gastroenterol. 2016;40(6):730–8.

    CAS  Article  Google Scholar 

  78. Ma H, Shi X, Yuan X, Ding Y. IL-1beta siRNA adenovirus benefits liver regeneration by improving mesenchymal stem cells survival after acute liver failure. An Hepatol. 2016;15(2):260–70.

    CAS  Google Scholar 

  79. Chen X, Gan Y, Li W, Su J, Zhang Y, Huang Y, et al. The interaction between mesenchymal stem cells and steroids during inflammation. Cell Death Dis. 2014;5:e1009.

    CAS  Article  Google Scholar 

  80. Wang K, Li Y, Zhu T, Zhang Y, Li W, Lin W, et al. Overexpression of c-Met in bone marrow mesenchymal stem cells improves their effectiveness in homing and repair of acute liver failure. Stem Cell Res Ther. 2017;8(1):162.

    Article  CAS  Google Scholar 

  81. Ma HC, Shi XL, Ren HZ, Yuan XW, Ding YT. Targeted migration of mesenchymal stem cells modified with CXCR4 to acute failing liver improves liver regeneration. World J Gastroenterol. 2014;20(40):14884–94.

    CAS  Article  Google Scholar 

  82. Fiore EJ, Bayo JM, Garcia MG, Malvicini M, Lloyd R, Piccioni F, et al. Mesenchymal stromal cells engineered to produce IGF-I by recombinant adenovirus ameliorate liver fibrosis in mice. Stem Cells Devel. 2015;24(6):791–801.

    CAS  Article  Google Scholar 

  83. Xie C, Xie DY, Lin BL, Zhang GL, Wang PP, Peng L, et al. Interferon-beta gene-modified human bone marrow mesenchymal stem cells attenuate hepatocellular carcinoma through inhibiting AKT/FOXO3a pathway. Br J Cancer. 2013;109(5):1198–205.

    CAS  Article  Google Scholar 

  84. Studeny M, Marini FC, Champlin RE, Zompetta C, Fidler IJ, Andreeff M. Bone marrow-derived mesenchymal stem cells as vehicles for interferon-beta delivery into tumors. Res. 2002;62(13):3603–8.

    CAS  Google Scholar 

  85. Su Y, Cheng R, Zhang J, Qian J, Diao C, Ran J, et al. Interferon-alpha2b gene-modified human bone marrow mesenchymal stem cells inhibit hepatocellular carcinoma by reducing the Notch1 levels. Life Sci. 2015;143:18–26.

    CAS  Article  Google Scholar 

  86. Sun XY, Nong J, Qin K, Lu H, Moniri MR, Dai LJ, et al. MSC(TRAIL)-mediated HepG2 cell death in direct and indirect co-cultures. Anticancer Res. 2011;31(11):3705–12.

    CAS  Google Scholar 

  87. Zhang B, Shan H, Li D, Li ZR, Zhu KS, Jiang ZB. The inhibitory effect of MSCs expressing TRAIL as a cellular delivery vehicle in combination with cisplatin on hepatocellular carcinoma. Cancer Biol Ther. 2012;13(12):1175–84.

    CAS  Article  Google Scholar 

  88. Chen XC, Wang R, Zhao X, Wei YQ, Hu M, Wang YS, et al. Prophylaxis against carcinogenesis in three kinds of unestablished tumor models via IL12-gene-engineered MSCs. Carcinogenesis. 2006;27(12):2434–41.

    CAS  Article  Google Scholar 

  89. Zhang Q, Yuan XF, Lu Y, Li ZZ, Bao SQ, Zhang XL, et al. Surface expression of anti-CD3scfv stimulates locoregional immunotherapy against hepatocellular carcinoma depending on the E1A-engineered human umbilical cord mesenchymal stem cells. Int J Cancer. 2017;141(7):1445–57.

    CAS  Article  Google Scholar 

  90. Niess H, Bao Q, Conrad C, Zischek C, Notohamiprodjo M, Schwab F, et al. Selective targeting of genetically engineered mesenchymal stem cells to tumor stroma microenvironments using tissue-specific suicide gene expression suppresses growth of hepatocellular carcinoma. Ann Surg. 2011;254(5):767–74 (Discussion 74–5).

    Article  Google Scholar 

  91. Zagoura DS, Roubelakis MG, Bitsika V, Trohatou O, Pappa KI, Kapelouzou A, et al. Therapeutic potential of a distinct population of human amniotic fluid mesenchymal stem cells and their secreted molecules in mice with acute hepatic failure. Gut. 2012;61(6):894–906.

    CAS  Article  Google Scholar 

  92. Gazdic M, Markovic BS, Arsenijevic A, Jovicic N, Acovic A, Harrell CR, et al. Crosstalk between mesenchymal stem cells and T regulatory cells is crucially important for the attenuation of acute liver injury. Liver Transpl. 2018;24(5):687–702.

    Article  Google Scholar 

  93. Parekkadan B, van Poll D, Megeed Z, Kobayashi N, Tilles AW, Berthiaume F, et al. Immunomodulation of activated hepatic stellate cells by mesenchymal stem cells. Biochem Biophys Res Commun. 2007;363(2):247–52.

    CAS  Article  Google Scholar 

  94. Hyun J, Wang S, Kim J, Kim GJ, Jung Y. MicroRNA125b-mediated Hedgehog signaling influences liver regeneration by chorionic plate-derived mesenchymal stem cells. Sci Rep. 2015;5:14135.

    CAS  Article  Google Scholar 

  95. Caplan AI. Mesenchymal stem cells: time to change the name! Stem Cells Translat Med. 2017;6(6):1445–51.

    Article  Google Scholar 

  96. de Oliveira GL, de Lima KW, Colombini AM, Pinheiro DG, Panepucci RA, Palma PV, et al. Bone marrow mesenchymal stromal cells isolated from multiple sclerosis patients have distinct gene expression profile and decreased suppressive function compared with healthy counterparts. Cell Transplant. 2015;24(2):151–65.

    Article  Google Scholar 

  97. Peng L, Li H, Gu L, Peng XM, Huang YS, Gao ZL. Comparison of biological characteristics of marrow mesenchymal stem cells in hepatitis B patients and normal adults. World J Gastroenterol. 2007;13(11):1743–6.

    Article  Google Scholar 

  98. Rombouts WJ, Ploemacher RE. Primary murine MSC show highly efficient homing to the bone marrow but lose homing ability following culture. Leukemia. 2003;17(1):160–70.

    CAS  Article  Google Scholar 

  99. Oh EJ, Lee HW, Kalimuthu S, Kim TJ, Kim HM, Baek SH, et al. In vivo migration of mesenchymal stem cells to burn injury sites and their therapeutic effects in a living mouse model. J Controlled Release. 2018;279:79–88.

    CAS  Article  Google Scholar 

  100. Schneider RK, Mullally A, Dugourd A, Peisker F, Hoogenboezem R, Van Strien PMH, et al. Gli1(+) mesenchymal stromal cells are a key driver of bone marrow fibrosis and an important cellular therapeutic target. Cell Stem Cell. 2018;23(2):308–9.

    CAS  Article  Google Scholar 

  101. Li M, Zhang YX, Zhang Z, Zhou XY, Zuo XL, Cong Y, et al. Endomicroscopy will track injected mesenchymal stem cells in rat colitis models. Inflamm Bowel Dis. 2015;21(9):2068–77.

    Article  Google Scholar 

  102. Ribot EJ, Gaudet JM, Chen Y, Gilbert KM, Foster PJ. In vivo MR detection of fluorine-labeled human MSC using the bSSFP sequence. Int J Nanomed. 2014;9:1731–9.

    Article  Google Scholar 

  103. Gonzalez-Lara LE, Xu X, Hofstetrova K, Pniak A, Chen Y, McFadden CD, et al. The use of cellular magnetic resonance imaging to track the fate of iron-labeled multipotent stromal cells after direct transplantation in a mouse model of spinal cord injury. Mol Imag Biol. 2011;13(4):702–11.

    Article  Google Scholar 

  104. Forbes SJ, Gupta S, Dhawan A. Cell therapy for liver disease: from liver transplantation to cell factory. J Hepatol. 2015;62(1 Suppl):S157–69.

    CAS  Article  Google Scholar 

  105. Panteleev AV, Vorob’ev IA. Expression of early hematopoietic markers in cord blood and mobilized blood. Tsitologiia. 2012;54(10):774–82.

    CAS  Google Scholar 

  106. Martinez-Agosto JA, Mikkola HK, Hartenstein V, Banerjee U. The hematopoietic stem cell and its niche: a comparative view. Genes Dev. 2007;21(23):3044–60.

    CAS  Article  Google Scholar 

  107. Mizukoshi E, Kaneko S. Immune cell therapy for hepatocellular carcinoma. J Hematol Oncol. 2019;12(1):52.

    Article  Google Scholar 

  108. Asahara T, Murohara T, Sullivan A, Silver M, van der Zee R, Li T, et al. Isolation of putative progenitor endothelial cells for angiogenesis. Science. 1997;275(5302):964–7.

    CAS  Article  Google Scholar 

  109. Kaushal S, Amiel GE, Guleserian KJ, Shapira OM, Perry T, Sutherland FW, et al. Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo. Nat Med. 2001;7(9):1035–40.

    CAS  Article  Google Scholar 

  110. Satija NK, Singh VK, Verma YK, Gupta P, Sharma S, Afrin F, et al. Mesenchymal stem cell-based therapy: a new paradigm in regenerative medicine. J Cell Mol Med. 2009;13(11–12):4385–402.

    CAS  Article  Google Scholar 

  111. Dominici M, Le Blanc K, Mueller I, Slaper-Cortenbach I, Marini F, Krause D, et al. Minimal criteria for defining multipotent mesenchymal stromal cells The International Society for Cellular Therapy position statement. Cytotherapy. 2006;8(4):315–7.

    CAS  Article  Google Scholar 

  112. Huang L, Zhang C, Gu J, Wu W, Shen Z, Zhou X, et al. A randomized, placebo-controlled trial of human umbilical cord blood mesenchymal stem cell infusion for children with cerebral palsy. Cell Transplant. 2018;27(2):325–34.

    Article  Google Scholar 

  113. Mohamadnejad M, Alimoghaddam K, Mohyeddin-Bonab M, Bagheri M, Bashtar M, Ghanaati H, et al. Phase 1 trial of autologous bone marrow mesenchymal stem cell transplantation in patients with decompensated liver cirrhosis. Arch Iran Med. 2007;10(4):459–66.

    CAS  Google Scholar 

  114. Jang YO, Kim YJ, Baik SK, Kim MY, Eom YW, Cho MY, et al. Histological improvement following administration of autologous bone marrow-derived mesenchymal stem cells for alcoholic cirrhosis: a pilot study. Liver Int. 2014;34(1):33–41.

    CAS  Article  Google Scholar 

  115. Kantarcioglu M, Demirci H, Avcu F, Karslioglu Y, Babayigit MA, Karaman B, et al. Efficacy of autologous mesenchymal stem cell transplantation in patients with liver cirrhosis. Turk J Gastroenterol. 2015;26(3):244–50.

    Article  Google Scholar 

  116. Sakai Y, Takamura M, Seki A, Sunagozaka H, Terashima T, Komura T, et al. Phase I clinical study of liver regenerative therapy for cirrhosis by intrahepatic arterial infusion of freshly isolated autologous adipose tissue-derived stromal/stem (regenerative) cell. Regenerat Ther. 2017;6:52–64.

    Article  Google Scholar 

  117. Zhang Y-C, Liu W, Fu B-S, Wang G-Y, Li H-B, Yi H-M, et al. Therapeutic potentials of umbilical cord–derived mesenchymal stromal cells for ischemic-type biliary lesions following liver transplantation. Cytotherapy. 2017;19(2):194–99.

    CAS  Article  Google Scholar 

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Acknowledgements

This manuscript was edited by one or more of the highly qualified native English-speaking editors at American Journal Experts (certificate verification key: E53E-CABE-7BDF-5D05-B576).

Funding

This project was supported by National Key R&D Program of China (Grant No. 2018YFA0107500); and National Natural Science Foundation of China (Grant No. 31700788, 81973599, 81772940, 81630070, 81872243).

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  1. Tumor Immunology and Gene Therapy Center, Shanghai Eastern Hepatobiliary Surgery Hospital, 225 Changhai Road, Shanghai, 200438, China

    Xue Yang, Yan Meng, Zhipeng Han, Fei Ye, Lixin Wei & Chen Zong

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  1. Xue Yang
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  2. Yan Meng
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  3. Zhipeng Han
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LXW and CZ formulated the idea. XY and CZ wrote the manuscript. XY and YM made the figure and the table. ZPH and FY critically revised the manuscript. All authors read and approved the final manuscript.

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Correspondence to Chen Zong.

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Yang, X., Meng, Y., Han, Z. et al. Mesenchymal stem cell therapy for liver disease: full of chances and challenges. Cell Biosci 10, 123 (2020). https://doi.org/10.1186/s13578-020-00480-6

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  • DOI: https://doi.org/10.1186/s13578-020-00480-6

Keywords

  • Mesenchymal stem cells
  • Liver disease
  • Cell therapy

Cell & Bioscience

ISSN: 2045-3701

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