Putative Immunogenicity Expression Profiling Using Human Pluripotent Stem Cells and Derivatives

Author:

Awe Jason P.1,Gschweng Eric H.23,Vega-Crespo Agustin1,Voutila Jon1,Williamson Mary H.1,Truong Brian1,Kohn Donald B.2345,Kasahara Noriyuki16,Byrne James A.13

Affiliation:

1. Department of Molecular and Medical Pharmacology, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

2. Department of Microbiology, Immunology, and Molecular Genetics, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

3. Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

4. Department of Pediatrics, Mattel Children's Hospital, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

5. Jonsson Comprehensive Cancer Center, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

6. Department of Medicine, UCLA School of Medicine, University of California, Los Angeles, Los Angeles California, USA

Abstract

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.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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