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CD4 T 细胞有助于髓系细胞介导杀伤免疫逃逸肿瘤。

CD4 T cells help myeloid-mediated killing of immune-evasive tumors.

机构信息

Division of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.

Division of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.

出版信息

Trends Cancer. 2023 Oct;9(10):777-779. doi: 10.1016/j.trecan.2023.07.013. Epub 2023 Aug 5.

DOI:10.1016/j.trecan.2023.07.013
PMID:37544796
Abstract

In a recent study published in Nature, Kruse et al. demonstrated an indirect tumor-killing mechanism orchestrated by a small number of CD4 effector T cells. These CD4 T cells can reprogram myeloid cells not just into IFNγ-induced antigen-presenting cells but also into iNOS-expressing tumoricidal effectors that can eradicate immune-evasive tumors.

摘要

在最近发表在《自然》杂志上的一项研究中,克吕泽等人展示了一种由少数 CD4 效应 T 细胞协调的间接肿瘤杀伤机制。这些 CD4 T 细胞不仅可以将髓样细胞重新编程为 IFNγ 诱导的抗原呈递细胞,还可以编程为表达 iNOS 的肿瘤杀伤效应器,从而根除免疫逃避肿瘤。

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CD4 T cells help myeloid-mediated killing of immune-evasive tumors.CD4 T 细胞有助于髓系细胞介导杀伤免疫逃逸肿瘤。
Trends Cancer. 2023 Oct;9(10):777-779. doi: 10.1016/j.trecan.2023.07.013. Epub 2023 Aug 5.
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CD4+ T cells in adoptive immunotherapy and the indirect mechanism of tumor rejection.过继性免疫治疗中的CD4+ T细胞与肿瘤排斥的间接机制。
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The role of CD4 T cells in rejection of solid tumors.CD4 T细胞在实体瘤排斥反应中的作用。
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Myeloid-derived suppressor cells attenuate TH1 development through IL-6 production to promote tumor progression.髓源性抑制细胞通过产生白细胞介素-6来抑制 TH1 细胞的发育,从而促进肿瘤的进展。
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Tumour-specific CD4 T cells eradicate melanoma via indirect recognition of tumour-derived antigen.肿瘤特异性CD4 T细胞通过间接识别肿瘤衍生抗原来根除黑色素瘤。
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Immunosuppressive myeloid cells induced by chemotherapy attenuate antitumor CD4+ T-cell responses through the PD-1-PD-L1 axis.化疗诱导的免疫抑制性髓系细胞通过 PD-1-PD-L1 轴减弱抗肿瘤 CD4+ T 细胞反应。
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Murine CD4+ T cell responses are inhibited by cytotoxic T cell-mediated killing of dendritic cells and are restored by antigen transfer.细胞毒性 T 细胞介导的树突状细胞杀伤抑制了小鼠 CD4+ T 细胞反应,并通过抗原转移得到恢复。
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Adoptive transfer of tumor-primed, in vitro-activated, CD4+ T effector cells (TEs) combined with CD8+ TEs provides intratumoral TE proliferation and synergistic antitumor response.过继转移经肿瘤致敏、体外激活的CD4⁺ 效应T细胞(TEs)与CD8⁺ TEs联合使用,可实现肿瘤内TE增殖和协同抗肿瘤反应。
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Mutations in glioblastoma proteins do not disrupt epitope presentation and recognition, maintaining a specific CD8 T cell immune response potential.胶质母细胞瘤蛋白的突变不会破坏抗原表位的呈递和识别,从而保持了特定的 CD8 T 细胞免疫反应潜能。
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