Immunogenicity and tumorigenicity of pluripotent stem cells and their derivatives: genetic and epigenetic perspectives.

One aim of stem cell-based therapy is to utilize pluripotent stem cells (PSCs) as a supplementary source of cells to repair or replace tissues or organs that have ceased to function due to severe tissue damage. However, PSC-based therapy requires extensive research to ascertain if PSC derivatives are functional without the risk of tumorigenicity, and also do not engender severe immune rejection that threatens graft survival and function. Recently, the suitability of induced pluripotent stem cells applied for patient-tailored cell therapy has been questioned since the discovery of several genetic and epigenetic aberrations during the reprogramming process. Hence, it is crucial to understand the effect of these abnormalities on the immunogenicity and survival of PSC grafts. As induced PSC-based therapy represents a hallmark for the potential solution to prevent and arrest immune rejection, this review also summarizes several up-to-date key findings in the field.

INTRODUCTION

PSCs are capable of differentiating into almost all types of cells and hold great promise as an alternative source for cell-based therapy. Before large scale expansion of clinical compatible PSCs, direct differentiation into a given cell type, and structural and functional integration into transplanted organs can be clinically applied, concerns over immune rejection and potential tumorigenesis will need to be addressed.

IMMUNOGENICITY AND VARIABILITY OF PLURIPOTENT STEM CELLS

The assumption that patient-derived or syngeneic induced PSCs (iPSCs) will be immune-tolerated has since been disputed by studies completed by Zhao et al. [1]. This study demonstrated that both retroviral and episomal-derived iPSCs showed immune rejection after transplantation into C57BL/6 mice, compared to embryonic stem cells (ESCs). Expression analysis revealed that regressing teratomas commonly overexpressed two genes that contribute to an increase in immunogenicity, Hormad1 and Zg16. Evidently, more recent studies have been conducted that contradict these initial findings. Concerns over the method of immunogenicity assessment, number of clones tested, and reprogramming efficacy have led to corrective measures and a more critical evaluation of the immunogenicity of iPSC-derived tissues. A subsequent study assessed immunogenicities of ESCs and iPSCs using three assays - teratoma formation, skin transplantation and bone marrow transplantation - on five ESC and seven iPSC lines to obtain more conclusive results [2]. Reports revealed that differentiated cells developed from iPSCs elicit limited immune responses, with no physiologic correlation between basal, endogenous expression of Hormad1 and Zg16 and syngeneic graft survival [2, 3].

Nevertheless, further investigation into the immunogenicity of iPSC-derived tissue will be needed before use in a clinical setting. For example, variation among iPSC clones due to partial reprogramming or differential developmental stages can trigger an immune response during transplantation [2]. One study revealed that the human immune system possesses a natural ability to detect pluripotency antigen Oct4 through memory T cells [4]. It seems that residual undifferentiated cells would need to be eliminated before transplantation to avoid an immune response to Oct4 as well as teratoma formation. In addition, there are still concerns over the influence of genetic background on the reprogramming process, as well as the introduction of genetic instability during this process. Reports have demonstrated that iPSC lines generated from the same individual show expression signatures more similar to one another than to those from different individuals [5], and that certain mouse strains were more efficient at generating iPSCs than others [6]. Furthermore, reprogramming methods that do not involve genomic integration have been shown to be less prone to immune attacks and have a lower teratoma-forming propensity after transplantation [1, 7]. Nonetheless, single nucleotide polymorphism and whole genome copy number variation analyses have revealed a higher frequency of genomic variations that arise after reprogramming, during the prolonged iPSC maintenance, and as a result of differentiation [8, 9].Therefore, establishing standardized methods of reprogramming that elicit a minimal immune response would be beneficial before applications in a clinical setting.

As cell replacement therapy would involve transplantation of differentiated iPSCs into patients, another concern is increased immunogenicity involved with the differentiation process. Work with ESCs has shown variability in MHC expression and increased immunogenicity after differentiation [10, 11]. As a precaution, immunosuppressive drug regimens can be used to manipulate the recipients’ immune system to accommodate transplantation of iPSC-derived tissue. However, there are several pitfalls to this, such as an increased risk for opportunistic infections, drug toxicities, and potential inhibition of graft maturation and function [12-14]. If in vitro modifications to iPSCs can be avoided, chance of host rejection will be reduced. Therefore, quality controls to avoid changes in antigen presentation and in genetic alterations during differentiation of iPSCs in combination with immunosuppressive measures will be instrumental in promoting graft acceptance.

UNDIFFERENTIATED PSCS EXPRESS LOW LEVELS OF MAJOR HISTOCOMPATIBILITY COMPLEX ANTIGENS AND CO-STIMULATORY MOLECULES

Major histocompatibility complex (MHC) molecules in mouse or human leukocyte antigens (HLAs) in human have been identified as one of the major impediments in the development of transplantation. High polymorphism of MHC molecules attributes pertinently to the immunological barrier between organ donors and recipients, and incompatibility of MHCs leads to acute graft rejection [15, 16].

Although the immunogenicity of PSCs and their derivatives remains elusive, it has been shown that undifferentiated but not differentiated PSCs possess immune privilege properties. Early studies have demonstrated that human ESCs (hESCs) have low expression of MHC class I, and complete absence of MHC class II antigens and co-stimulatory molecules (CD80 and CD86) [17-19]. Yet, when MHC molecules are up-regulated during ESC differentiation and/or during in vitro interferon-gamma (IFNγ) stimulation, immune rejection is accelerated [17, 18]. Mouse ESC-derived insulin producing cell clusters were shown to have higher MHC expression, compared to undifferentiated ESCs of origin. In addition to differentiation, increased immunogenicity of undifferentiated ESCs after IFNγ treatment was reported by several studies, all of which concurred to similar results that no teratomas or only quickly regressing teratomas were formed [19-21] (Fig. ). These findings suggest the possibility of PSC-derived graft failure, if transplanted into an unfavorable environment that promotes the upregulation of MHC molecules [22].

Successful generation of iPSCs seems to herald the possibility for development of “customized” patient-specific cells and tissues to circumvent both ethic concerns and MHC barriers. Ideally, autologous iPSCs will be a perfect immunological match due to their lack of alloantigens to trigger graft rejection. Similar to ESCs, Suárez-Álvarez and colleagues have confirmed the low expression of MHC class I and β2m, as well as the lack of MHC class II in iPSCs. During the process of differentiation, an upsurge of MHC expression was observed, particularly with a drastic boost in MHC class I and β2m, after formation of embryoid body (EB) structures (a common procedure used in PSC differentiation) [23]. Overall, these studies suggest that MHC expression on PSCs is inducible and dynamically regulated, consequently implicating the immunogenic potential of PSCs and their progeny after tissue specification and cytokine treatment.

EPIGENETIC REGULATION CONTRIBUTES TO INCREASED IMMUNE RECOGNITION OF DIFFERENTIATED PSCS

Extending the notion of increased MHC expression during differentiation of iPSCs and ESCs demands for an in-depth investigation of its regulation mechanisms. Suárez-Álvarez et al. proposed an epigenetic mechanism to regulate MHC expression during differentiation. In undifferentiated hESCs and iPSCs, as a major epigenetic repression mechanism in gene expression, MHC class II and CIITA genes (the essential transcriptional factor for MHC class II expression) were found to be hypermethylated. Bisulfide sequencing and analysis of CpG methylation profiles all concluded that the absence of MHC class II expression in hESCs and iPSCs was controlled via heavy DNA methylation of these genes. Importantly, this hypermethylation status of MHC class II and its associated genes was barely changed after differentiation. This finding is in agreement with the previous observation that MHC class II was neither expressed nor up-regulated during differentiation or after IFNγ stimulation [23]. Considering the restricted expression pattern of MHC class II in nature, if PSC differentiation does not enhance MHC class II expression, then PSC-derived grafts are unlikely to carry professional antigen presenting cells (APCs) that could directly comprise engraftment via acute rejection.

In contrast to MHC class II genes, components of MHC class I antigen processing machinery genes showed demethylation, which corresponds to enhanced expression in differentiated iPSCs; indicative of an increased susceptibility to rejection. Although MHC molecules act critically in antigen presentation, the complexity of this process requires signals other than MHC antigens. Early efforts have examined the expression of costimulatory molecules (CD40, CD80 and CD86) on PSCs. Similar to MHC class II expression, both differentiation and IFNγ treatment did not increase the expression of costimulatory molecules in human ESCs, and therefore regulation is possibly through a DNA methylation mechanism [17, 23, 24]. Presumably, the lack of costimulatory molecule expression on PSCs further impairs their ability to function as APCs.

In addition to DNA methylation, histone modification provides alternative strategies leading to the MHC expression profile unique in ESCs and iPSCs. Posttranslational modification of the amino-terminal tails of core histones acts in the regulation of gene expression and other diverse biological processes. Depending on the type and number of histone modifications, epigenetic modified histone could either activate or repress gene expression. By performing ChiP assays, Suárez-Álvarez and colleagues showed that H3K9me3 (repressive histone marker) maintained a high degree at MHC class II loci during ESC differentiation. In contrast, 60-fold greater H3K4me3 (active promoter marker) at MHC class I and β2m regions was observed in differentiated iPSCs and hESCs, coincident with the increased β2m mRNA level. It is known that lack of β2m in cells will limit the expression of MHC class I trimeric molecule on the cell surface. Histone modification of H3K4me3 in MHC class I genes post differentiation facilitated chromatin relaxation and allowed gene expression [23]. Expression of Tapasin (TPN), an antigen processing machinery family member, is also repressed by H3K9me3 in undifferentiated PSCs while upregulated by H3K4me3 in differentiated PSCs. TPN is a TAP (transporter associated with antigen processing)-associated glycoprotein and an ER chaperone. It is uniquely dedicated to MHC class I biosynthesis [23]. TPN binds MHC class I molecules and integrates into peptide-loading complexes. Formation of an "optimal peptide" bond allows MHC class I to be released and exported to the cell surface for presentation to T cells [24-26] (Fig. ). The repression on TPN in undifferentiated PSCs could contribute to low MHC class I expression. It is undeniable that epigenetic regulation is fundamentally associated with controlling MHC expression in ESCs and iPSCs, and provides tantalizing strategies for inducing tolerance for stem cells grafts. However, this study has yet to directly assess the time points for the series of events that lead to enhanced MHC expression in comparison with other embryonic antigen expression. The risk posed by presenting embryonic antigens to a host immune system could result in the destruction of even syngeneic iPSCs by NK cells and T cell-mediated rejection due to an inherent ability to recognize embryonic antigens, as described above.

EPIGENETIC MEMORY

Gene profiling studies have revealed some aberrant epigenetic patterns and even residual epigenetic memories from the cell type of origin in iPSCs [27]. With emerging evidence, it raises the concerns of whether disrupted epigenetic patterns in iPSCs will compromise their suitability for clinical application in regenerative medicine.

Differentiated somatic cells have distinctive epigenetic patterns to maintain their cell identity, whereas cellular reprogramming works to break the epigenetic barrier of differentiated cells back to an undifferentiated state [27]. Somatic cell nucleus transfer (SCNT) techniques facilitate a transfer of somatic cell nuclei into enucleated unfertilized or recently fertilized oocytes [27]. Of the current reprogramming methods, SCNT is believed to generate iPSCs closest to the ESC pluripotent state. Kim and colleagues compared iPSCs generated from SCNT and the typical Yamanaka transcription factor-based reprogramming method for alternations in DNA methylation [28]. Strikingly, there were remarkable epigenetic signatures left over from the somatic cell of origin, even though iPSCs from both methods established the defined ESC phenotype. The epigenetic landscape of SCNT-generated iPSCs revealed relatively much less deviation from those of authentic ESCs. They further investigated the differentiation potential of iPSCs derived from the two methods, which alternatively confirmed residual epigenetic memory in iPSCs. There was high propensity for iPSCs to differentiate into their cell type of origin; osteogenic and hematopoietic cells. Nonetheless, epigenetic abnormalities caused by forced expression of the four Yamanaka factors in early reprogramming process could be ameliorated by repetitive subculture and subsequent passaging [28]. However, certain epigenetic defects would not be completely corrected, and consequently, this reduces the flexibility of iPSCs and limits their future application in regenerative medicine.

Ultimately, it is relevant to ask whether it is really possible to coerce iPSCs to a pluripotency “ground-zero” state, similar to ESCs. The goal for using iPSCs is to utilize their capacity of self-renewal and differentiation to generate patient-specific cells and tissues. Rather than focusing on how close iPSCs are to matching authentic ESCs, one could take advantage of epigenetic memory. If the target treatment demands for a specific cell type, iPSC lines based from close lineage would eliminate difficulties associated with targeted differentiation. For example, Bar-Nur et al. demonstrated that beta cell-derived iPSCs have a greater propensity to differentiate into insulin-producing cells [29]. Moreover, it seems that low immunogenic lineages could be generated from iPSCs derived from cells with inherent low immunogenicity. Recently, Liu et al. have successfully generated a population of neural progenitor cells with relatively low immunogenicity from iPSCs derived from umbilical cord mesenchymal cells (UMCs). As the cell of origin, UMCs have long been proven to be less immunogenic than other somatic fibroblasts used commonly in reprogramming. Authors showed that UMC-derived iPSCs and their differentiated lineages retain low immunogenicity of UMCs [30]. This observation reflects the presence of epigenetic memory in iPSCs and may hold new promises to develop stem cell-based therapy with low immunogenicity by utilizing epigenetic memories.

PLURIPOTENT STEM CELLS MEET THE IMMUNE SYSTEM: INNATE IMMUNE RESPONSES TO PSCS

Innate immunity is the first line of defense and is comprised of fast responding immune cells, including all granulocytes and natural killer (NK) cells. It carries the responsibility of generating an immediate wave of inflammatory reaction towards a graft after transplantation [22, 31, 32]. Even though innate immune cells do not require antigen specificity, they function as a bridge for full activation of the adaptive immune system through the process of antigen presentation.

MHC molecules create a sense of “self” in host immune systems. Both ESCs and iPSCs are characterized to be immune privileged by their low expression of MHC molecules to evade T cell mediated immune responses [15, 19]. However, loss of “self” entity on cell surfaces, similar to tumor cells, is the specialized forte of NK cell killing. Absence or mismatch of MHC class I on ESC-derived tissue would therefore lead to the premise of increased graft susceptibility to NK cell recognition and damage. Hanna et al. first studied the immunologic barrier of NK cells in iPSC-derived hematopoietic progenitor cells (HPCs) and found a rejection of engraftment [33]. In support of this finding, others later reported that undifferentiated ESCs and ESC-derived progenitor cells were more prone to NK cell attack due to expression of NK cell activating ligands. One study compared the susceptibility of undifferentiated ESCs and ESC-derived HPCs in the matter of NK mediated lysis. High levels of H60, an activating ligand to Natural Killer group 2 D (NKG2D), contributed to NK cell mediated destruction of ESC-derived HPCs in a perforin-granzyme dependent manner [34]. Admittedly, balance of MHC expression on PSCs and their derivatives is critical for the involvement of NK cells in graft rejection. Tabayoyong et al. showed that the enhancement of MHC class I expression via IFNγ stimulation would be protective for HPCs against NK cell cytotoxicity [34]. One study further concluded that IFNγ mediated up-regulation of MHC class I is critical in syngeneic transplant survival of ESC-derived vascular progenitor cells by evading NK cell-mediated lysis [26] (Fig. ).

Contrary to the aforementioned findings, in the scenario of fetal development, absence of MHC class II and low levels of MHC class I at the maternal-fetal interface promotes maternal immunosuppression [35, 36]. Additional signals, besides MHC class I, are also utilized to establish fetomaternal tolerance. For instance, HLA-G and HLA-E are non-classical MHC class Ib molecules that are essential in the acceptance of an embryo. To investigate whether PSCs also take advantage of these molecules, a study conducted by Yen et al. revealed that hESC-derived mesenchymal progenitor cells (MPCs) were resistant to NK cell lysis, coinciding with high HLA-G expression on the surface [37]. Furthermore, several reports claimed that this resistance to NK cell cytotoxicity exists, by showing contradicting results in NKG2D ligand expression. Frenzel et al. revealed that NKG2D ligands were expressed on murine ESCs but not on ESC-derived cardiomyocytes (ESCM), protecting ESC-derived progeny from NK cell recognition and lysis [38].

To analyze these disparities, it is important to consider the differential responses posed by different NK cell subtypes, and account for the level of activation in the setting of in vitro assays. Given the challenges in grasping the balance of inhibitory and stimulatory signals in NK cells and the dynamic regulation of MHC expression, it is likely that discrepancies on whether PSCs promote/evade NK cell-mediated cytotoxicity will continue.

Granulocytes, macrophages and neutrophils, contribute to early inflammation attacks as an immediate immune response after transplantation. Neutrophils and macrophages are instantly recruited and infiltrated into the site of ESC-derived insulin producing cell cluster implants with robust inflammatory cytokine and chemokine excretion [20, 21]. Although innate responses are likely to eventually subside, it is unclear as to what extent adaptive immunity has been evoked and graft function has been damaged after this inflammatory assault. It is clear that the immune system cannot simply be dichotomized into two isolated compartments. Given that early innate inflammatory responses lay the basis for later adaptive immune activation, effective control of innate inflammatory responses should improve long-term engraftment.

PLURIPOTENT STEM CELLS MEET THE IMMUNE SYSTEM: ADAPTIVE IMMUNE RESPONSES TO UNDIFFERENTIATED PSCS AND THEIR DIFFERENTIATED PROGENIES

Adaptive immunity generates antigen specific immune responses. Without immunosuppression, the outcome of allogeneic transplantation is graft rejection mediated by CD4 and/or CD8 T cells [39]. Activation of the adaptive immune system facilitates a subsequent expansion of specific recipient T helper cells via either donor or recipient APC. As aforementioned, PSCs are unlikely to function as APCs owing to the absence of MHC class II and costimulatory molecules. However, the immunogenic outcomes of engraftment remain uncertain, especially for PSC-derived epithelial cells. Under certain conditions, epithelial cells, the unconventional APCs, could acquire antigen presentation capacity leading to graft failure by directly activating allogeneic T cells [40]. Nevertheless, in stem cell-based transplantation, graft damage and subsequent functional failure are most likely due to indirect antigen presentation-mediated T cell response. CD4+ T helper cells do not directly lyse target cells expressing allogeneic MHC molecules. Rather, they orchestrate the entire immune rejection response by aiding activation of donor specific immune cells; B cell and cytotoxic T lymphocytes (CTL). The majority of graft damage and succeeding functional failure is caused by CTL-induced lysis through binding to MHC class I on donor cells [15-17, 39]. In general, ESCs and iPSCs exhibit low immunogenicity with low expression levels of MHC class I molecules and undetectable levels of MHC class II and costimulatory molecules. Early studies have suggested that undifferentiated hESCs are incapable of inducing allogeneic T cell proliferation in mixed leukocyte reactions in vitro. Similarly, undifferentiated murine ESCs and early EB cells expressing lymphocytic choriomeningitis virus (LCMV) peptides showed resistance to LCMV-specific CTL lysis [41]. In contrast, Dressel et al. argued that murine ESCs loaded with OVA peptide were subjected to OVA-specific TCR transgenic T cell recognition and subsequent antigen-specific lysis [42]. In this experimental setting, they used a pure OVA specific T effector cell population instead of a T cell mixture with diverse specificity, which might undermine inhibitory effects observed by other groups [43]. It is possible that indirect allorecognition of iPSCs and ESCs in prolonged engraftment may take place when recipient APCs pick up ESC- or iPSC-derived antigens to CD4+ T cells (Fig. ).

Several potential mechanisms for suppressing host immune response mediated by PSCs have been proposed. Inhibition on T cell proliferation and activation is thought to occur via Arginase I expression on the surface of ESCs. Consumption of L-arginine in the localized environment impairs proper activation of T cells, which would theoretically be reversed by supplementing L-arginine back into culture media [44]. Our group found that addition of high levels of L-arginine did not ameliorate suppression on T cell proliferation, suggesting other coexisting mechanisms. We found that, similar to intact cells, the cellular protein extracts from both undifferentiated mouse and human ESCs retain immunomodulation properties. ESC-derived soluble factors were able to suppress T cell proliferation and to impede DC maturation. T cells exposed to soluble ESC cellular factors also showed a reduced Th1 cytokine production and transcriptional profile. The potential mechanism was likely through inhibition of PKC-θ phosphorylation[45, 46]. In addition, ESCs have been reported to regulate the local microenvironment to favor T regulatory (Treg) cell polarization to acquire immune privilege. Treg is a unique subset of T cells, which can suppress T effector cells with diverse antigen specificities. Induction or recruitment of Treg into the graft is an ideal outcome in transplantation. Once activated, Treg will reinforce an establishment of tolerance and acquirement of immune privilege [47-49]. In one study, a transplanted murine EB graft was accepted by an allogeneic recipient only in combination with non-depleting anti-CD8 antibody [49-51]. The greater proportion of infiltrating T cells in the tolerated graft was found to be FoxP3+. Even so, future studies should be conducted to clarify how ESCs interfere with T cell polarization, and what the underlying mechanisms are.

Taken together, the majority of reports and proposed mechanisms support a reduced immunogenicity of undifferentiated PSCs. One would ask whether their differentiated progeny is still capable of retaining these properties after an increase in MHC class I expression. In the context of stem cell-based therapy, the immunological properties of the cell type of interest after differentiation from either ESCs or iPSCs should be assessed to determine their suitability in clinical application. Currently, few studies have been reported regarding whether iPSCs possess the same immune inhibitory property as do ESCs. Kim and colleagues showed that iPSC-derived HPCs induce anergy in allogeneic CTL [52]. They speculated that induced T cell anergy was due to poor expression of MHC and co-stimulatory molecules. Though MHC class I expression was augmented with IFNγ stimulation, the co-stimulatory molecule was unaffected. It would be interesting to examine whether anergy can be generated in iPSC-derived tissues other than HPC/immune cells. In a number of clinical reports, co-transplantation of donor HPC/bone marrow together with other tissues has been shown to enhance engraftment [53-55]. To this context, co-transplantation of hESC-derived HPC or immune cells together with other hESC-derivatives has been considered as one strategy to reduce immune rejection. It is possible that long-term protection from CTL-mediated killing could be an optimistic outlook in the future development of ESC- or iPSC-based therapeutics.

TO BEHAVE AS A CANCER CELL OR NOT TO BEHAVE

One promising aspect of iPSC technology is the potential use in cell replacement therapy to treat numerous debilitating diseases. However, concerns over the immunogenicity and tumorigenicity of these cells has proven challenging when considering clinical applications. Immune evasion is a desired characteristic for iPSCs, but problematic when utilized by cancer cells, as it promotes tumor growth and development.

Whereas iPSC technology is struggling with complications involving immunogenicity, cancer cells are constantly evolving to escape or silence immune responses in order for a tumor to thrive in its microenvironment. Initially the immune system is able to protect the host against tumor development through immunosurveillance, which inadvertently leads to immune evasion by progression through three stages of immunoediting; elimination, equilibrium, escape [56-58]. There are several strategies that tumor cells employ during immune evasion, some of which include MHC class I structural alterations/downregulation [59, 60], mutations of Fas or TRAIL [61, 62], and inhibition of T cell receptors and/or development of Treg [63, 64]. Many of the same mechanisms are used by undifferentiated pluripotent stem cells, however, clinical transplantations would involve differentiated progenies that do not share these characteristics, and therefore additional steps need to be taken to ensure reduced immunogenicity after transplantation.

Not only is there an immunogenicity concern for iPSC use in clinical therapy, but there is also an inherent tumorigenicity risk associated with iPSCs as well. Evidently, many of the genes responsible for pluripotency induction are aberrantly expressed in cancer [65, 66]. Gene expression microarray studies done by Riggs et al. found that both iPSCs and oncogenic foci upregulated the glycolysis pathway and had substantial overlap in gene expression changes, indicating that induced pluripotency and oncogenic transformation are related processes [67]. Supporting this notion, another study revealed that both iPSCs and cancer cells suppress Lefty expression, a tumor suppressor protein, whereas ESCs show normal expression levels [68]. iPSC-based therapies pose the risk of introducing chromosomal damage and genomic instability during iPSC derivation, selecting for tumorigenic clones, producing incompletely differentiated and aberrantly methylated cells during differentiation and culturing, as well as contaminating therapeutic cells and reactivating pluripotency transgenes during transplantation (reviewed by Lee et al.) [69].

Despite these clinical hurdles to iPSC-based therapies, progress has been made towards decreasing the risk of tumor formation after transplantation. One method involves removing the oncogene c-Myc, which contributes to tumorigenesis through overstimulating cell growth/metabolism and promoting genomic instability during reprogramming [70, 71]. Additionally, a shift towards insertion-free procedures for generating iPSCs has already been developed, given that viral methods are a risk for mutagenesis and subsequent tumorigenesis [72]. Together with other attempts to improve the quality of iPSCS, such as specific protein inhibitors [73], substitution [70, 71], use of microRNAs [74, 75] or even small molecules [76], advances in this area look promising. Lastly, precaution during selection of the somatic origin of iPSCs should be exercised, as Miura et al. found that cell lines derived from mouse tail-tip fibroblasts and hepatocytes had a higher teratoma-forming propensity than other tissue origins [7, 77]. This is likely due to an increased resistance to differentiation in these cell lines, which may be associated with epigenetic regulation machinery.

IPSCS FOR POTENTIAL TUMOR THERAPY, NOT INITIATION

Despite concern for tumorigenesis, iPSC technology has generated enthusiasm in the field of cancer therapy. In particular, iPSCs can be differentiated into immune cells, such as T cells and NK cells. By taking advantage of epigenetic memory, it may be possible to reprogram T cells with certain tumor antigens into iPSCs, then differentiate them back and expand the population before infusion back into a patient [78, 79]. Indeed, Themeli et al. have successfully combined iPSC and chimeric antigen receptor (CAR) technologies to generate T cells targeting CD19 that was expressed by malignant B cells, which potently inhibits tumor growth in a xenograft model [80]. Several studies have also focused on generating NK cells because of their anti-tumor effects without the need for antigen matching or previous exposure [81, 82]. iPSC-mediated immunotherapy can prevent relapse and immune rejection, and decrease tumor burden [83]. In addition, Li et al. investigated the possibility of using PSCs to develop a cancer vaccine [84]. In this paper, the premise that several oncofetal antigens are shared between cancer and stem cells led to the hypothesis that the immune response against these embryonic antigens would be cross reactive in targeting cancer antigens, and therefore generate protective immunity against tumors. Indeed, mice immunized with hESCs and iPSCs evoked stronger cellular and humoral immune responses against colon carcinoma through an expansion of tumor specific IFNγ producing cells and a coinciding reduction of myeloid suppressive cells. Although the vaccination with iPSCs to relieve tumor burden or establish tumor protection was not fully successful, this area is likely a promising modality that warrants further investigation. Using less heterogenic iPSCs and combining other immune approaches may help to achieve this goal. Lastly, another area where iPSCs will be useful is for replacement of damaged tissue caused by radiation, chemotherapy, or surgery [78]. Successful engraftment of liver has already been shown to be effective [85]. In summary, provided that the necessary steps are taken to circumvent tumorigenicity, iPSCs could prove to be an efficient and effective means for cancer treatment.