Major histocompatibility complex class II in the tumor microenvironment: functions of nonprofessional antigen-presenting cells

被引:5
|
作者
Macy, Anne M. [1 ,2 ]
Herrmann, Lauren M. [1 ,2 ]
Adams, Anngela C. [1 ,2 ]
Hastings, K. Taraszka [1 ,2 ,3 ]
机构
[1] Univ Arizona, Coll Med Phoenix, 425 N 5th St, Phoenix, AZ 85004 USA
[2] Phoenix Vet Affairs Hlth Care Syst, 650 E Indian Sch Rd, Phoenix, AZ 85023 USA
[3] Univ Arizona, Univ Arizona Canc Ctr, 1515 N Campbell Ave, Tucson, AZ 85724 USA
基金
美国国家卫生研究院;
关键词
LYSOSOMAL THIOL REDUCTASE; HLA-DR EXPRESSION; LYMPHOCYTE INFILTRATION; MOLECULAR MARKERS; MELANOMA-CELLS; TRANSACTIVATOR; CARCINOMA; SURVIVAL; CANCER; EPITHELIUM;
D O I
10.1016/j.coi.2023.102330
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Major histocompatibility complex class-II-restricted presentation by nonprofessional antigen-presenting cells in the tumor microenvironment can regulate antitumor T-cell responses. In murine models, tumor cell-specific MHC class II expression decreases in vivo tumor growth, dependent on T cells. Tumor cell-specific MHC class II expression is associated with improved survival and response to immune checkpoint inhibitors in human cancers. Antigen-presenting cancer-associated fibroblasts (apCAF) present MHC class-II-restricted antigens and activate CD4 T cells. The role of MHC class II on apCAFs depends on the cell of origin. MHC class II on tumoral lymphatic endothelial cells leads to expansion of regulatory T cells and increased in vivo tumor growth.
引用
收藏
页数:9
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