Restriction of PD-1 function by cis -PD-L1/CD80 interactions is required for optimal T cell responses
Autor: | Kenji Shimizu, Takeo K. Maeda, Takumi Maruhashi, Il-mi Okazaki, Tatsuya Takemoto, Taku Okazaki, Daisuke Sugiura |
---|---|
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Multidisciplinary biology Effector Chemistry medicine.medical_treatment T cell Immunotherapy Plasma protein binding medicine.disease_cause Autoimmunity Cell biology 03 medical and health sciences 030104 developmental biology 0302 clinical medicine medicine.anatomical_structure Immune system 030220 oncology & carcinogenesis PD-L1 medicine biology.protein CD80 |
Zdroj: | Science. 364:558-566 |
ISSN: | 1095-9203 0036-8075 |
DOI: | 10.1126/science.aav7062 |
Popis: | 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 |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |