Subsets of exhausted CD8
Animals
Antibodies, Blocking
/ immunology
CD8-Positive T-Lymphocytes
/ drug effects
Cell Line, Tumor
Female
Humans
Lymphocyte Subsets
/ drug effects
Lymphocytes, Tumor-Infiltrating
/ drug effects
Lymphocytic Choriomeningitis
/ immunology
Lymphocytic choriomeningitis virus
/ drug effects
Melanoma, Experimental
/ immunology
Mice, Congenic
Mice, Inbred C57BL
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Journal
Nature immunology
ISSN: 1529-2916
Titre abrégé: Nat Immunol
Pays: United States
ID NLM: 100941354
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
12
06
2018
accepted:
03
01
2019
entrez:
20
2
2019
pubmed:
20
2
2019
medline:
2
5
2019
Statut:
ppublish
Résumé
T cell dysfunction is a hallmark of many cancers, but the basis for T cell dysfunction and the mechanisms by which antibody blockade of the inhibitory receptor PD-1 (anti-PD-1) reinvigorates T cells are not fully understood. Here we show that such therapy acts on a specific subpopulation of exhausted CD8
Identifiants
pubmed: 30778252
doi: 10.1038/s41590-019-0312-6
pii: 10.1038/s41590-019-0312-6
pmc: PMC6673650
mid: NIHMS1026478
doi:
Substances chimiques
Antibodies, Blocking
0
Programmed Cell Death 1 Receptor
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
326-336Subventions
Organisme : NCATS NIH HHS
ID : KL2 TR002542
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI056299
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007627
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007753
Pays : United States
Organisme : NIAID NIH HHS
ID : K23 AI130408
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009172
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI133524
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI115712
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA207021
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : ErratumIn
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