Restriction of PD-1 function by cis -PD-L1/CD80 interactions is required for optimal T cell responses

Author:

Sugiura Daisuke1ORCID,Maruhashi Takumi1ORCID,Okazaki Il-mi1ORCID,Shimizu Kenji1ORCID,Maeda Takeo K.1ORCID,Takemoto Tatsuya2,Okazaki Taku1ORCID

Affiliation:

1. Division of Immune Regulation, Institute of Advanced Medical Sciences, Tokushima University, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.

2. Laboratory for Embryology, Institute of Advanced Medical Sciences, Tokushima University, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.

Abstract

Sparing T cells from inhibition Programmed cell death 1 (PD-1) is an inhibitory receptor that normally keeps T cell immune responses in check. Immunotherapy targeting PD-1 has proven successful for certain types of cancer, but it remains unclear how PD-1 is regulated. Sugiura et al. found that a costimulatory molecule, CD80, can restrict PD-1 function during the activation of T lymphocytes. Binding of CD80 to the PD-1 ligand PD-L1 in cis on primary activated dendritic cells interfered with the ability of PD-L1 to access PD-1 on T cells, which would otherwise have inhibited T cell activation. Functional insights into PD-L1–CD80 interactions may explain the outcomes of anti–PD-1 and anti–PD-L1 cancer therapy. Science , this issue p. 558

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology, Japan Science and Technology Agency

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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