| Literature DB >> 25575527 |
Jason P Awe1, Eric H Gschweng1, Agustin Vega-Crespo1, Jon Voutila1, Mary H Williamson1, Brian Truong1, Donald B Kohn1, Noriyuki Kasahara1, James A Byrne2.
Abstract
Autologous human induced pluripotent stem cells (hiPSCs) should allow cellular therapeutics without an associated immune response. This concept has been controversial since the original report that syngeneic mouse iPSCs elicited an immune response after transplantation. However, an investigative analysis of any potential acute immune responses in hiPSCs and their derivatives has yet to be conducted. In the present study, we used correlative gene expression analysis of two putative mouse "immunogenicity" genes, ZG16 and HORMAD1, to assay their human homologous expression levels in human pluripotent stem cells and their derivatives. We found that ZG16 expression is heterogeneous across multiple human embryonic stem cell and hiPSC-derived cell types. Additionally, ectopic expression of ZG16 in antigen-presenting cells is insufficient to trigger a detectable response in a peripheral blood mononuclear cell coculture assay. Neither of the previous immunogenicity-associated genes in the mouse currently appears to be relevant in a human context. ©AlphaMed Press.Entities:
Keywords: HORMAD1; Human embryonic stem cell; Human induced pluripotent stem cell; Immunogenicity; Peripheral blood mononuclear cells; ZG16
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Year: 2015 PMID: 25575527 PMCID: PMC4303355 DOI: 10.5966/sctm.2014-0117
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 6.940