Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Trends Mol Med. 2022 Nov;28(11):951-963. doi: 10.1016/j.molmed.2022.08.006. Epub 2022 Sep 5.
The highly immunosuppressive and heterogeneous milieu of brain malignancies contributes to their dismal prognosis. Regardless of their cellular origin, brain tumors grow in an environment with various specialized organ-resident cells. Although homeostatic microglia contribute to a healthy brain, conversations between disease-associated microglia and T cells compromise their individual and collective capacity to curb malignant growth. We review the mechanisms of T cell-microglia interactions and discuss how their collaboration fosters heterogeneity and immunosuppression in brain cancers. Because of the importance of microglia and T cells in the brain tumor microenvironment, it is crucial to understand their interactions to derive innovative therapeutics.
脑恶性肿瘤具有高度免疫抑制和异质性的微环境,这导致了其预后不良。无论其细胞起源如何,脑肿瘤都在具有各种特化器官驻留细胞的环境中生长。尽管稳态小胶质细胞有助于大脑健康,但与疾病相关的小胶质细胞和 T 细胞之间的对话损害了它们单独和集体抑制恶性生长的能力。我们综述了 T 细胞与小胶质细胞相互作用的机制,并讨论了它们的协作如何促进脑癌的异质性和免疫抑制。由于小胶质细胞和 T 细胞在脑肿瘤微环境中的重要性,了解它们的相互作用对于获得创新性治疗至关重要。