The tumor immune microenvironment and T-cell-related immunotherapies in colorectal cancer

被引:2
|
作者
Liu, Chuang [1 ]
Ju, Qifeng [2 ]
Yu, Shaolei [1 ]
机构
[1] Heilongjiang Univ Chinese Med, Affiliated Hosp 2, Hanan Branch, Guogoli St, Harbin, Peoples R China
[2] Heilongjiang Univ Chinese Med, Affiliated Hosp 1, Harbin, Peoples R China
关键词
Colorectal cancer; Tumor immune microenvironment; T cell; Monoclonal antibody; CAR-T; DNA MISMATCH REPAIR; MHC CLASS-I; COLON-CANCER; PD-1; BLOCKADE; SOLID TUMORS; OPEN-LABEL; COMPLEMENT; RECEPTOR; DIFFERENTIATION; ACTIVATION;
D O I
10.1007/s12672-024-01117-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumor microenvironment includes a complex network of immune T-cell subsets that play important roles in colorectal cancer (CRC) progression and are key elements of CRC immunotherapy. T cells develop and migrate within tumors, recognizing tumor-specific antigens to regulate immune surveillance. Current immunotherapies are divided into the following main categories based on the regulatory role of T-cell subsets in the tumor immune microenvironment (TIME): cytokines, monoclonal antibodies, peptide vaccines, CAR-T cells and more. This review describes the composition of the tumor immune microenvironment in colorectal cancer and the involvement of T cells in the pathogenesis and progression of CRC as well as current T-cell-related immunotherapies. Further studies on CRC-specific tumor antigens, the gene regulation of T cells, and the regulation of immune activity are needed.
引用
收藏
页数:13
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