| Literature DB >> 30926234 |
Spencer C Wei1, Roshan Sharma2, Nana-Ama A S Anang1, Jacob H Levine3, Yang Zhao4, James J Mancuso1, Manu Setty3, Padmanee Sharma5, Jing Wang4, Dana Pe'er6, James P Allison7.
Abstract
Co-stimulation regulates T cell activation, but it remains unclear whether co-stimulatory pathways also control T cell differentiation. We used mass cytometry to profile T cells generated in the genetic absence of the negative co-stimulatory molecules CTLA-4 and PD-1. Our data indicate that negative co-stimulation constrains the possible cell states that peripheral T cells can acquire. CTLA-4 imposes major boundaries on CD4+ T cell phenotypes, whereas PD-1 subtly limits CD8+ T cell phenotypes. By computationally reconstructing T cell differentiation paths, we identified protein expression changes that underlied the abnormal phenotypic expansion and pinpointed when lineage choice events occurred during differentiation. Similar alterations in T cell phenotypes were observed after anti-CTLA-4 and anti-PD-1 antibody blockade. These findings implicate negative co-stimulation as a key regulator and determinant of T cell differentiation and suggest that checkpoint blockade might work in part by altering the limits of T cell phenotypes.Entities:
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Year: 2019 PMID: 30926234 PMCID: PMC6664799 DOI: 10.1016/j.immuni.2019.03.004
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745