Institute of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.
Cell Immunol. 2012 Sep;279(1):21-4. doi: 10.1016/j.cellimm.2012.08.004. Epub 2012 Sep 14.
Tumor-specific T cells must overcome a multitude of suppressive mechanisms to destroy cancerous cells effectively. Furthermore, it appears that the tumor microenvironment facilitates the development of highly immunosuppressive T cells, which may also allow subsequent tumor progression. In colorectal cancer, the relationship between regulatory T cells (e.g. FoxP3(+) Tregs) and tumor prognosis and progression is less clear, despite their well-documented ability to impinge on anti-tumor immune responses. Here we explore our current knowledge of colorectal TIL heterogeneity, deciphering subsets which may be of benefit or detriment.
肿瘤特异性 T 细胞必须克服多种抑制机制才能有效地破坏癌细胞。此外,肿瘤微环境似乎有利于高度免疫抑制性 T 细胞的发展,这也可能允许随后的肿瘤进展。在结直肠癌中,尽管调节性 T 细胞(如 FoxP3(+)Tregs)具有抑制抗肿瘤免疫反应的能力,但它们与肿瘤预后和进展之间的关系并不明确。在这里,我们探讨了结直肠肿瘤浸润淋巴细胞(TIL)异质性的现有知识,解析了可能有益或有害的亚群。