| Literature DB >> 29093272 |
Nathalie E Blachère1,2, Dana E Orange1,3,4, Emily C Gantman1,5, Bianca D Santomasso1,6, Graeme C Couture1, Teresa Ramirez-Montagut1,7, John Fak1, Kevin J O'Donovan1,8, Zhong Ru1, Salina Parveen1, Mayu O Frank1,4, Michael J Moore1,9, Robert B Darnell1,2,4.
Abstract
In the course of modeling the naturally occurring tumor immunity seen in patients with paraneoplastic cerebellar degeneration (PCD), we discovered an unexpectedly high threshold for breaking CD8+ cytotoxic T cell (CTL) tolerance to the PCD autoantigen, CDR2. While CDR2 expression was previously found to be strictly restricted to immune-privileged cells (cerebellum, testes, and tumors), unexpectedly we have found that T cells also express CDR2. This expression underlies inhibition of CTL activation; CTLs that respond to epithelial cells expressing CDR2 fail to respond to T cells expressing CDR2. This was a general phenomenon, as T cells presenting influenza (flu) antigen also fail to activate otherwise potent flu-specific CTLs either in vitro or in vivo. Moreover, transfer of flu peptide-pulsed T cells into flu-infected mice inhibits endogenous flu-specific CTLs. Our finding that T cells serve as a site of immune privilege, inhibiting effector CTL function, uncovers an autorepressive loop with general biologic and clinical relevance.Entities:
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Year: 2017 PMID: 29093272 PMCID: PMC5752293 DOI: 10.1172/jci.insight.96173
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708