STING-dependent cytosolic DNA sensing mediates innate immune recognition of immunogenic tumors

Spontaneous T cell responses against tumors occur frequently and have prognostic value in patients. The mechanism of innate immune sensing of immunogenic tumors leading to adaptive T cell responses remains undefined, although type I interferons (IFNs) are implicated in this process. We found that sp...

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Vydáno v:Immunity (Cambridge, Mass.) Ročník 41; číslo 5; s. 830
Hlavní autoři: Woo, Seng-Ryong, Fuertes, Mercedes B, Corrales, Leticia, Spranger, Stefani, Furdyna, Michael J, Leung, Michael Y K, Duggan, Ryan, Wang, Ying, Barber, Glen N, Fitzgerald, Katherine A, Alegre, Maria-Luisa, Gajewski, Thomas F
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 20.11.2014
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ISSN:1097-4180, 1097-4180
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Shrnutí:Spontaneous T cell responses against tumors occur frequently and have prognostic value in patients. The mechanism of innate immune sensing of immunogenic tumors leading to adaptive T cell responses remains undefined, although type I interferons (IFNs) are implicated in this process. We found that spontaneous CD8(+) T cell priming against tumors was defective in mice lacking stimulator of interferon genes complex (STING), but not other innate signaling pathways, suggesting involvement of a cytosolic DNA sensing pathway. In vitro, IFN-? production and dendritic cell activation were triggered by tumor-cell-derived DNA, via cyclic-GMP-AMP synthase (cGAS), STING, and interferon regulatory factor 3 (IRF3). In the tumor microenvironment in vivo, tumor cell DNA was detected within host antigen-presenting cells, which correlated with STING pathway activation and IFN-? production. Our results demonstrate that a major mechanism for innate immune sensing of cancer occurs via the host STING pathway, with major implications for cancer immunotherapy.
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ISSN:1097-4180
1097-4180
DOI:10.1016/j.immuni.2014.10.017