CXCL9型
CD8型
肿瘤微环境
CXCR3型
免疫系统
趋化因子
免疫学
免疫
癌症研究
T细胞
细胞毒性T细胞
生物
医学
趋化因子受体
体外
生物化学
作者
Paola Marcovecchio,Graham D. Thomas,Shahram Salek‐Ardakani
标识
DOI:10.1136/jitc-2020-002045
摘要
Tumor-associated macrophages (TAMs) are among the main contributors to immune suppression in the tumor microenvironment, however, TAM depletion strategies have yielded little clinical benefit. Here, we discuss the concept that TAMs are also key regulators of anti-PD(L)-1-mediated CD8 T cell-dependent immunity. Emerging data suggest that expression of the chemokine CXCL9 by TAMs regulates the recruitment and positioning of CXCR3-expressing stem-like CD8 T (T stem ) cells that underlie clinical responses to anti-PD(L)-1 treatment. We evaluate clinical and mechanistic studies that establish relationships between CXCL9-expressing TAMs, T stem and antitumor immunity. Therapies that enhance anti-PD(L)-1 response rates must consider TAM CXCL9 expression. In this perspective, we discuss opportunities to enhance the frequency and function of CXCL9 expressing TAMs and draw on comparative analyzes from infectious disease models to highlight potential functions of these cells beyond T stem recruitment.
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