CD300f信号传导诱导抑制人单核/巨噬细胞

IF 3.7 4区 医学 Q2 CELL BIOLOGY Cellular immunology Pub Date : 2023-08-01 DOI:10.1016/j.cellimm.2023.104731
Sarah I.M. Sutherland , Xinsheng Ju , Pablo A. Silveira , Fiona Kupresanin , Lisa G. Horvath , Georgina J. Clark
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引用次数: 0

摘要

CD300糖蛋白是一个相关的白细胞表面分子家族,通过其成对的触发和抑制受体调节免疫反应。在这里,我们研究了CD300f,一种凋亡细胞受体,以及它如何调节人类单核细胞和巨噬细胞的功能。我们发现,通过与抗CD300f mAb(DCR-2)交联的CD300f信号传导抑制单核细胞,导致抑制分子CD274(PD-L1)的上调及其对T细胞增殖的抑制。此外,CD300f信号传导驱动巨噬细胞优先向M2型表达,CD274上调,IL-4进一步增强了CD274的表达。CD300f信号传导激活单核细胞中的PI3K/Akt通路。CD300f交联引起的PI3K/Akt信号传导的抑制导致单核细胞上CD274表达的下调。这些发现突出了CD300f阻断在癌症免疫治疗中的潜在用途,以靶向肿瘤微环境中的免疫抑制巨噬细胞,这是对PD-1/PD-L1检查点抑制剂的已知耐药性机制。
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CD300f signalling induces inhibitory human monocytes/macrophages

The CD300 glycoproteins are a family of related leucocyte surface molecules that regulate the immune response via their paired triggering and inhibitory receptors. Here we studied CD300f, an apoptotic cell receptor, and how it modulates the function of human monocytes and macrophages. We showed that CD300f signalling by crosslinking with anti-CD300f mAb (DCR-2) suppressed monocytes causing upregulation of the inhibitory molecule, CD274 (PD-L1) and their inhibition of T cell proliferation. Furthermore, CD300f signalling drove macrophages preferentially towards M2-type with upregulation of CD274, which was further enhanced by IL-4. CD300f signalling activates the PI3K/Akt pathway in monocytes. Inhibition of PI3K/Akt signalling resulting from CD300f crosslinking leads to downregulation of CD274 expression on monocytes. These findings highlight the potential use of CD300f blockade in cancer immune therapy to target immune suppressive macrophages in the tumour microenvironment, a known resistance mechanism to PD-1/PD-L1 checkpoint inhibitors.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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