| Literature DB >> 24362036 |
Zachary S Scheiner1, Sohel Talib, Ellen G Feigal.
Abstract
Induced pluripotent stem cell (iPSC) technology offers the promise of immune-matched cell therapies for a wide range of diseases and injuries. It is generally assumed that cells derived from autologous iPSCs will be immune-privileged. However, there are reasons to question this assumption, including recent studies that have tested iPSC immunogenicity in various ways with conflicting results. Understanding the risk of an immune response and developing strategies to minimize it will be important steps before clinical testing. Here, we review the evidence for autologous iPSC immunogenicity, its potential causes, and approaches for assessment and mitigation.Entities:
Keywords: Cell Therapy; Cellular Immune Response; Humoral Response; Induced Pluripotent Stem Cells; Innate Immunity; iPSC
Mesh:
Year: 2013 PMID: 24362036 PMCID: PMC3931018 DOI: 10.1074/jbc.R113.509588
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157