Role of inflammasome activation in tumor immunity triggered by immune checkpoint blockers.
Animals
Antineoplastic Agents, Immunological
/ therapeutic use
Apyrase
/ antagonists & inhibitors
CD8-Positive T-Lymphocytes
/ immunology
Humans
Inflammasomes
/ immunology
Membrane Proteins
/ antagonists & inhibitors
Neoplasm Proteins
/ antagonists & inhibitors
Neoplasms
/ drug therapy
Th17 Cells
/ immunology
Cancer
checkpoint blockade
immunotherapy
inflammasome
Journal
Clinical and experimental immunology
ISSN: 1365-2249
Titre abrégé: Clin Exp Immunol
Pays: England
ID NLM: 0057202
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
08
10
2019
revised:
17
03
2020
accepted:
19
03
2020
entrez:
17
4
2020
pubmed:
17
4
2020
medline:
21
10
2020
Statut:
ppublish
Résumé
Immune checkpoint blockers improve the overall survival of a limited number of patients among different cancers. Identifying pathways that influence the immunological and clinical response to treatment is critical to improve the therapeutic efficacy and predict clinical responses. Recently, a key role has been assigned to innate immune mechanisms in checkpoint blockade-driven anti-tumor responses. However, inflammatory pathways can both improve and impair anti-tumor immunity. In this review, we discuss how different inflammatory pathways, particularly inflammasome activation, can influence the clinical outcome of immune checkpoint blockers. Inflammasome activation may reinforce anti-tumor immunity by boosting CD8
Identifiants
pubmed: 32297328
doi: 10.1111/cei.13433
pmc: PMC7160664
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Inflammasomes
0
Membrane Proteins
0
Neoplasm Proteins
0
TMEM176B protein, human
0
Apyrase
EC 3.6.1.5
ENTPD1 protein, human
EC 3.6.1.5
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
155-162Informations de copyright
© 2020 British Society for Immunology.
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