| Literature DB >> 29531164 |
Peter T Sage1,2, Frank A Schildberg1,2, Raymond A Sobel3, Vijay K Kuchroo2,4,5, Gordon J Freeman6, Arlene H Sharpe7,2,8.
Abstract
The programmed death (PD)-1 coinhibitory receptor regulates the balance between T cell activation and tolerance. Although the PD-1 ligands, PD-L1 and PD-L2, are expressed on a variety of cell types, the cell type-specific functions of PD-1 ligands in inducing signals through PD-1 are unknown. In this study, we use PD-L1 conditional knockout mice to investigate the cell type-specific functions of PD-L1. We demonstrate that PD-L1 expressed on dendritic cells (DCs), and to a lesser extent on B cells, attenuates the progression of experimental autoimmune encephalomyelitis and inhibits naive and effector T cells. PD-1 is highly expressed on effector populations, including T follicular helper (Tfh) cells and T follicular regulatory (Tfr) cells, which reside in germinal centers. We also show that DC PD-L1 is essential for limiting Tfh and Tfr cell differentiation. In addition, we find that PD-1 suppresses Tfh cell differentiation and help for Ig class switching, even in the presence of wild-type Tfr cells. Our work points to critical roles for PD-L1 expressed on DCs in mediating PD-1 functions.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29531164 PMCID: PMC6054131 DOI: 10.4049/jimmunol.1701231
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422