Tumor Microenvironment Center, University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Department of Immunology, University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
Clin Cancer Res. 2018 Jun 1;24(11):2473-2481. doi: 10.1158/1078-0432.CCR-17-0894. Epub 2018 Jan 31.
With the rapid rise of immunotherapy for cancer treatment, attention has focused on gaining a better understanding of T-cell biology in the tumor microenvironment. Elucidating the factors underlying changes in their function will allow for the development of new therapeutic strategies that could expand the patient population benefiting from immunotherapy, as well as circumvent therapy resistance. Cancers go beyond avoiding immune recognition and inducing T-cell dysfunction through coinhibitory molecules. Recent work has demonstrated that the tumor microenvironment elicits metabolic changes in T cells that dampen their ability to respond and that manipulating these metabolic changes can strengthen an antitumor immune response. Here we review the metabolic status of various types of T cells, the energetic state of the tumor microenvironment, and proposed modalities for improvement of immunotherapy through metabolic remodeling. .
随着癌症治疗中免疫疗法的迅速兴起,人们越来越关注在肿瘤微环境中更好地了解 T 细胞生物学。阐明其功能变化的原因将有助于开发新的治疗策略,从而扩大受益于免疫疗法的患者群体,并避免治疗耐药性。癌症不仅通过共抑制分子来避免免疫识别和诱导 T 细胞功能障碍。最近的工作表明,肿瘤微环境会引起 T 细胞的代谢变化,从而削弱其反应能力,而操纵这些代谢变化可以增强抗肿瘤免疫反应。在这里,我们综述了各种类型的 T 细胞的代谢状态、肿瘤微环境的能量状态,以及通过代谢重塑来改善免疫疗法的可能方式。