Impact of Immune Response on the Use of iPSCs in Disease Modeling

ISSN: 2212-3946 (Online)
ISSN: 1574-888X (Print)

Volume 10, 6 Issues, 2015

Download PDF Flyer

Current Stem Cell Research & Therapy

Aims & ScopeAbstracted/Indexed in

Submit Abstracts Online Submit Manuscripts Online

Anthony Atala
Wake Forest University School of Medicine,
Medical Center Boulevard
Winston Salem, NC 27157

View Full Editorial Board

Subscribe Purchase Articles Order Reprints

Current: 2.212
5 - Year: 2.428

Impact of Immune Response on the Use of iPSCs in Disease Modeling

Current Stem Cell Research & Therapy , 10(3): 236-244.

Author(s): Zimu Zhang, Biao Huang, Fei Gao and Rongxin Zhang.

Affiliation: Laboratory of Immunology and Inflammation, Research Center of Basic Medical Science, Tianjin Medical University, No.22 Qi Xiang Tai Road, Tianjin 300070, China.


It has been demonstrated that mouse and human somatic cells can be reprogrammed into an embryonic stem cell-like state by introducing combinations of the transcription factors. The generation of such induced pluripotent stem cells (iPSCs) has enabled the derivation of disease-specific pluripotent cells which opens up new avenues of disease modeling and provides valuable experimental platforms. Moreover, technologies for creating humanized animal models by human iPSCs will be available as well, which will increase the utility of humanized mice for research. Emerging evidences suggest, however, that immunogenicity of iPSCs seems to be a vital and controversial issue surrounding potential of iPSCs. Recent studies on induced multipotent progenitor cells (iMPCs) extend the applications of iPSC technology and provide promising candidates for disease modeling. In this review, we introduce a wide range of applications of iPSCs in disease modeling and discuss the immune response on the use of iPSCs as well as a promising alternative for future directions of disease modeling.


Disease modeling, immune response, immunogenicity, induced multipotent progenitor cells, induced pluripotent stem cells, reprogramming.

Purchase Online Order Reprints Order Eprints Rights and Permissions

Article Details

Volume: 10
Issue Number: 3
First Page: 236
Last Page: 244
Page Count: 9
DOI: 10.2174/1574888X09666140711120449

Related Journals

Webmaster Contact: Copyright © 2015 Bentham Science