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肿瘤驻留 CD8+T 细胞:IL-12 介导逆转肿瘤免疫抑制的关键催化剂。

Tumor-resident CD8+ T-cell: the critical catalyst in IL-12-mediated reversal of tumor immune suppression.

机构信息

Department of Microbiology and Immunology, School of Medicine and Biomedical Sciences, University at Buffalo, 138 Farber Hall, 3435 Main Street, Buffalo, NY 14214, USA.

出版信息

Arch Immunol Ther Exp (Warsz). 2010 Dec;58(6):399-405. doi: 10.1007/s00005-010-0097-7. Epub 2010 Sep 26.

Abstract

Tumor-resident T cells display a functionally impaired effector/memory (Tem) phenotype. Sustained intratumoral administration of IL-12, on the other hand, can restore cytolytic function to pre-existing CD8+ Tem, resulting in effective tumor kill. Whereas cytotoxic T lymphocytes (CTL) are generally assumed to mediate tumor regression via direct tumor cytotoxicity, recent work revealed that activated CD8+ Tem mobilize a systemic, multi-component effector cascade that includes both innate and adaptive immune mechanisms. Here we summarize these mechanisms, review how tumor-resident CD8+ Tem orchestrate this cascade and discuss the potential clinical implications of these findings.

摘要

肿瘤驻留 T 细胞表现出功能受损的效应/记忆 (Tem) 表型。另一方面,持续的肿瘤内给予白细胞介素-12 可以恢复预先存在的 CD8+ Tem 的细胞溶解功能,从而有效地杀死肿瘤。虽然细胞毒性 T 淋巴细胞 (CTL) 通常被认为通过直接肿瘤细胞毒性介导肿瘤消退,但最近的工作表明,激活的 CD8+ Tem 动员全身性多成分效应级联,包括先天和适应性免疫机制。在这里,我们总结了这些机制,回顾了肿瘤驻留的 CD8+ Tem 如何协调这一级联反应,并讨论了这些发现的潜在临床意义。

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