IL-15 is a component of the inflammatory milieu in the tumor microenvironment promoting antitumor responses.


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:
08 01 2019
Historique:
pubmed: 28 12 2018
medline: 13 3 2019
entrez: 28 12 2018
Statut: ppublish

Résumé

Previous studies have provided evidence that IL-15 expression within human tumors is crucial for optimal antitumor responses; however, the regulation of IL-15 within the tumor microenvironment (TME) is unclear. We report herein, in analyses of mice implanted with various tumor cell lines, soluble IL-15/IL-15Rα complexes (sIL-15 complexes) are abundant in the interstitial fluid of tumors with expression preceding the infiltration of tumor-infiltrating lymphocytes. Moreover, IL-15 as well as type I IFN, which regulates IL-15, was required for establishing normal numbers of CD8 T cells and natural killer cells in tumors. Depending on tumor type, both the tumor and the stroma are sources of sIL-15 complexes. In analyses of IL-15 reporter mice, most myeloid cells in the TME express IL-15 with CD11b

Identifiants

pubmed: 30587590
pii: 1814642116
doi: 10.1073/pnas.1814642116
pmc: PMC6329954
doi:

Substances chimiques

Il15ra protein, mouse 0
Interleukin-15 0
Membrane Proteins 0
Neoplasm Proteins 0
Receptors, Interleukin-15 0
Sting1 protein, mouse 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

599-608

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009598
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Rosa M Santana Carrero (RM)

Immunology Graduate Program, University of Texas (UT) MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX 77584.
Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Figen Beceren-Braun (F)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Sarai C Rivas (SC)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Shweta M Hegde (SM)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Achintyan Gangadharan (A)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Devin Plote (D)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.
Cancer Biology Graduate Program, University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX 77584.

Gabriel Pham (G)

Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Scott M Anthony (SM)

Immunology Graduate Program, University of Texas (UT) MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX 77584.
Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

Kimberly S Schluns (KS)

Immunology Graduate Program, University of Texas (UT) MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX 77584; kschluns@mdanderson.org.
Department of Immunology, University of Texas MD Anderson Cancer Center, Houston, TX 77584.

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Classifications MeSH