The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives

Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into all cell types in human body, and therefore hold great potential for cell therapy of currently incurable diseases including neural degenerative diseases, heart failure, and macular degeneration. This potenti...

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Main Authors: Xin Liu, Wenjuan Li, Xuemei Fu, Yang Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.00645/full
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author Xin Liu
Xin Liu
Wenjuan Li
Xuemei Fu
Yang Xu
Yang Xu
author_facet Xin Liu
Xin Liu
Wenjuan Li
Xuemei Fu
Yang Xu
Yang Xu
author_sort Xin Liu
collection DOAJ
description Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into all cell types in human body, and therefore hold great potential for cell therapy of currently incurable diseases including neural degenerative diseases, heart failure, and macular degeneration. This potential is further underscored by the promising safety and efficacy data from the ongoing clinical trials of hESC-based therapy of macular degeneration. However, one main challenge for the clinical application of hESC-based therapy is the allogeneic immune rejection of hESC-derived cells by the recipient. The breakthrough of the technology to generate autologous-induced pluripotent stem cells (iPSCs) by nuclear reprogramming of patient’s somatic cells raised the possibility that autologous iPSC-derived cells can be transplanted into the patients without the concern of immune rejection. However, accumulating data indicate that certain iPSC-derived cells can be immunogenic. In addition, the genomic instability associated with iPSCs raises additional safety concern to use iPSC-derived cells in human cell therapy. In this review, we will discuss the mechanism underlying the immunogenicity of the pluripotent stem cells and recent progress in developing immune tolerance strategies of human pluripotent stem cell (hPSC)-derived allografts. The successful development of safe and effective immune tolerance strategy will greatly facilitate the clinical development of hPSC-based cell therapy.
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spelling doaj.art-b55c730f12504d4580a588928d5981d52022-12-21T22:06:58ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-06-01810.3389/fimmu.2017.00645270365The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell DerivativesXin Liu0Xin Liu1Wenjuan Li2Xuemei Fu3Yang Xu4Yang Xu5Center for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaDivision of Biological Sciences, University of California, San Diego, La Jolla, CA, United StatesCenter for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe Eighth Affiliated Hospital of Sun Yat-sen University, Shenzhen, ChinaCenter for Regenerative and Translational Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaDivision of Biological Sciences, University of California, San Diego, La Jolla, CA, United StatesHuman embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into all cell types in human body, and therefore hold great potential for cell therapy of currently incurable diseases including neural degenerative diseases, heart failure, and macular degeneration. This potential is further underscored by the promising safety and efficacy data from the ongoing clinical trials of hESC-based therapy of macular degeneration. However, one main challenge for the clinical application of hESC-based therapy is the allogeneic immune rejection of hESC-derived cells by the recipient. The breakthrough of the technology to generate autologous-induced pluripotent stem cells (iPSCs) by nuclear reprogramming of patient’s somatic cells raised the possibility that autologous iPSC-derived cells can be transplanted into the patients without the concern of immune rejection. However, accumulating data indicate that certain iPSC-derived cells can be immunogenic. In addition, the genomic instability associated with iPSCs raises additional safety concern to use iPSC-derived cells in human cell therapy. In this review, we will discuss the mechanism underlying the immunogenicity of the pluripotent stem cells and recent progress in developing immune tolerance strategies of human pluripotent stem cell (hPSC)-derived allografts. The successful development of safe and effective immune tolerance strategy will greatly facilitate the clinical development of hPSC-based cell therapy.http://journal.frontiersin.org/article/10.3389/fimmu.2017.00645/fullembryonic stem cellsinduced pluripotent stem cellscell therapyallogeneic immune rejectionimmunogenicityimmune tolerance
spellingShingle Xin Liu
Xin Liu
Wenjuan Li
Xuemei Fu
Yang Xu
Yang Xu
The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
Frontiers in Immunology
embryonic stem cells
induced pluripotent stem cells
cell therapy
allogeneic immune rejection
immunogenicity
immune tolerance
title The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
title_full The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
title_fullStr The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
title_full_unstemmed The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
title_short The Immunogenicity and Immune Tolerance of Pluripotent Stem Cell Derivatives
title_sort immunogenicity and immune tolerance of pluripotent stem cell derivatives
topic embryonic stem cells
induced pluripotent stem cells
cell therapy
allogeneic immune rejection
immunogenicity
immune tolerance
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.00645/full
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