Your browser doesn't support javascript.
loading
VSIG4-expressing tumor-associated macrophages impair anti-tumor immunity.
Jung, Keunok; Jeon, You-Kyoung; Jeong, Dae Hoon; Byun, Jung Mi; Bogen, Bjarne; Choi, Inhak.
Afiliação
  • Jung K; Department of Microbiology and Immunology, Innovative Therapeutics Research Institute, Inje University College of Medicine, Republic of Korea.
  • Jeon YK; Department of Microbiology and Immunology, Innovative Therapeutics Research Institute, Inje University College of Medicine, Republic of Korea.
  • Jeong DH; Department of Obstetrics and Gynecology, Republic of Korea; Paik Institute for Clinical Research, Busan, Republic of Korea.
  • Byun JM; Department of Obstetrics and Gynecology, Republic of Korea; Paik Institute for Clinical Research, Busan, Republic of Korea.
  • Bogen B; Department of Immunology, Oslo University Hospital, Oslo, Norway.
  • Choi I; Department of Microbiology and Immunology, Innovative Therapeutics Research Institute, Inje University College of Medicine, Republic of Korea. Electronic address: miccih@inje.ac.kr.
Biochem Biophys Res Commun ; 628: 18-24, 2022 11 05.
Article em En | MEDLINE | ID: mdl-36063598
ABSTRACT
VSIG4, a newly identified co-inhibitory molecule belonging to the B7-related family, is exclusively expressed on tissue-resident macrophages and is involved in the suppression of T cell proliferation and cytokine production. We sought to characterize the role of VSIG4 in anti-tumor immunity in the tumor microenvironment, focusing on VSIG4-expressing tumor-associated macrophages (TAMs). We found that VSIG4-expressing TAMs negatively regulated antigen-specific T cell proliferation and cytokine production through direct inhibition via cell cycle arrest, but not apoptosis, as well as through their arginase 1 activity. Furthermore, VSIG4-expressing TAMs suppress tumor-specific CD8+ T cell cytotoxicity. Therefore, our results suggest that VSIG4-expressing TAMs could be a negative cellular regulator of anti-tumor immunity in the tumor microenvironment.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Complemento / Microambiente Tumoral / Macrófagos Associados a Tumor Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Complemento / Microambiente Tumoral / Macrófagos Associados a Tumor Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article