CD4
CD4(+) T helper 1 cells
T cell trafficking
checkpoint blockade
head and neck squamous cell carcinoma
immunotherapy
mechanisms of response
peripheral blood mononuclear cells
single-cell omics
tumor microenvironment
tumor-draining lymph node
Journal
Immunity
ISSN: 1097-4180
Titre abrégé: Immunity
Pays: United States
ID NLM: 9432918
Informations de publication
Date de publication:
01 Mar 2024
01 Mar 2024
Historique:
received:
26
12
2022
revised:
30
11
2023
accepted:
08
02
2024
pubmed:
6
3
2024
medline:
6
3
2024
entrez:
5
3
2024
Statut:
aheadofprint
Résumé
Cancer patients often receive a combination of antibodies targeting programmed death-ligand 1 (PD-L1) and cytotoxic T lymphocyte antigen-4 (CTLA4). We conducted a window-of-opportunity study in head and neck squamous cell carcinoma (HNSCC) to examine the contribution of anti-CTLA4 to anti-PD-L1 therapy. Single-cell profiling of on- versus pre-treatment biopsies identified T cell expansion as an early response marker. In tumors, anti-PD-L1 triggered the expansion of mostly CD8
Identifiants
pubmed: 38442708
pii: S1074-7613(24)00083-9
doi: 10.1016/j.immuni.2024.02.007
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests P.M.C. reports the mentioned grant and non-financial support from AstraZeneca during the study; personal fees and non-financial support from AbbVie, Bayer, Bristol-Myers Squibb, Merck, LEO Pharma, and Vifor Pharma; personal fees from Daiichii Sankyo, and Rakuten; and non-financial support from Teva, Novartis, Amgen, and Roche outside the submitted work.