Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
Front Immunol. 2020 Nov 27;11:593219. doi: 10.3389/fimmu.2020.593219. eCollection 2020.
Glioblastoma Multiforme (GBM) is the most common and aggressive form of intracranial tumors with poor prognosis. In recent years, tumor immunotherapy has been an attractive strategy for a variety of tumors. Currently, most immunotherapies take advantage of the adaptive anti-tumor immunity, such as cytotoxic T cells. However, the predominant accumulation of tumor-associated microglia/macrophages (TAMs) results in limited success of these strategies in the glioblastoma. To improve the immunotherapeutic efficacy for GBM, it is detrimental to understand the role of TAM in glioblastoma immunosuppressive microenvironment. In this review, we will discuss the roles of CD47-SIRPα axis in TAMs infiltration and activities and the promising effects of targeting this axis on the activation of both innate and adaptive antitumor immunity in glioblastoma.
多形性胶质母细胞瘤(GBM)是最常见和侵袭性的颅内肿瘤,预后不良。近年来,肿瘤免疫疗法已成为多种肿瘤的一种有吸引力的策略。目前,大多数免疫疗法利用适应性抗肿瘤免疫,如细胞毒性 T 细胞。然而,肿瘤相关的小胶质细胞/巨噬细胞(TAMs)的主要积累导致这些策略在胶质母细胞瘤中的效果有限。为了提高胶质母细胞瘤的免疫治疗效果,了解 TAM 在胶质母细胞瘤免疫抑制微环境中的作用是不利的。在这篇综述中,我们将讨论 CD47-SIRPα 轴在 TAMs 浸润和活性中的作用,以及靶向该轴对激活胶质母细胞瘤固有和适应性抗肿瘤免疫的有希望的影响。