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可溶性 SLAMF6 受体诱导强烈的 CD8 T 细胞效应功能,并提高抗黑色素瘤活性。

Soluble SLAMF6 Receptor Induces Strong CD8 T-cell Effector Function and Improves Anti-Melanoma Activity .

机构信息

Sharett Institute of Oncology, Hadassah Hebrew University Hospital, Jerusalem, Israel.

出版信息

Cancer Immunol Res. 2018 Feb;6(2):127-138. doi: 10.1158/2326-6066.CIR-17-0383. Epub 2018 Jan 5.

Abstract

SLAMF6, a member of the SLAM (signaling lymphocyte activation molecules) family, is a homotypic-binding immune receptor expressed on NK, T, and B lymphocytes. Phosphorylation variance between T-cell subclones prompted us to explore its role in anti melanoma immunity. Using a 203-amino acid sequence of the human SLAMF6 (seSLAMF6) ectodomain, we found that seSLAMF6 reduced activation-induced cell death and had an antiapoptotic effect on tumor-infiltrating lymphocytes. CD8 T cells costimulated with seSLAMF6 secreted more IFNγ and displayed augmented cytolytic activity. The systemic administration of seSLAMF6 to mice sustained adoptively transferred transgenic CD8 T cells in comparable numbers to high doses of IL2. In a therapeutic model, lymphocytes activated by seSLAMF6 delayed tumor growth, and when further supported with seSLAMF6, induced complete tumor clearance. The ectodomain expedites the loss of phosphorylation on SLAMF6 that occurs in response to T-cell receptor triggering. Our findings suggest that seSLAMF6 is a costimulator that could be used in melanoma immunotherapy. .

摘要

SLAMF6 是 SLAM(信号淋巴细胞激活分子)家族的成员,是一种在 NK、T 和 B 淋巴细胞上表达的同型结合免疫受体。T 细胞亚克隆之间的磷酸化差异促使我们探索其在抗黑色素瘤免疫中的作用。使用人 SLAMF6(seSLAMF6)胞外域的 203 个氨基酸序列,我们发现 seSLAMF6 减少了激活诱导的细胞死亡,并对肿瘤浸润淋巴细胞具有抗凋亡作用。与 seSLAMF6 共刺激的 CD8 T 细胞分泌更多的 IFNγ 并显示出增强的细胞毒性活性。将 seSLAMF6 系统给药给小鼠,可维持数量相当的过继转移转基因 CD8 T 细胞,与高剂量 IL2 一样有效。在治疗模型中,经 seSLAMF6 激活的淋巴细胞延迟肿瘤生长,并且当进一步用 seSLAMF6 支持时,诱导完全清除肿瘤。胞外域促进了 SLAMF6 上磷酸化的丧失,这种磷酸化是对 T 细胞受体触发的反应。我们的研究结果表明,seSLAMF6 是一种共刺激因子,可用于黑色素瘤免疫治疗。

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