Peripheral-derived regulatory T cells contribute to tumor-mediated immune suppression in a nonredundant manner.
KLF2
melanoma
pTregs
prostate cancer
regulatory T cells
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
03 Sep 2024
03 Sep 2024
Historique:
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
29
8
2024
Statut:
ppublish
Résumé
Identifying tumor-mediated mechanisms that impair immunity is instrumental for the design of new cancer therapies. Regulatory T cells (Tregs) are a key component of cancer-derived immune suppression; however, these lymphocytes are necessary to prevent systemic autoimmunity in mice and humans, and thus, direct targeting of Tregs is not a clinical option for cancer patients. We have previously demonstrated that excising transcription factor Kruppel-like factor 2 (
Identifiants
pubmed: 39207730
doi: 10.1073/pnas.2404916121
doi:
Substances chimiques
Kruppel-Like Transcription Factors
0
Klf2 protein, mouse
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2404916121Subventions
Organisme : NCI NIH HHS
ID : T32 CA009531
Pays : United States
Organisme : Elsa U. Pardee Foundation (EUPF)
ID : N/A
Organisme : NCI NIH HHS
ID : U01 CA196406
Pays : United States
Organisme : DOD | USA | MEDCOM | CDMRP | DOD Prostate Cancer Research Program (PCRP)
ID : PC140122
Organisme : NCI NIH HHS
ID : P30 CA022453
Pays : United States
Organisme : American Cancer Society (ACS)
ID : DBG-23-103670-01-IBCD
Déclaration de conflit d'intérêts
Competing interests statement:The authors declare no competing interest.