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γδ T 细胞在癌症中的治疗途径

英文原题:Therapeutic avenues for γδ T cells in cancer.

PubMed 2023/11/24(内容时间) J Immunother Cancer Q1 · IF 11.7(JCR 2025)

研究概要

γδ T细胞被视为下一代癌症免疫疗法的有前景的效应淋巴细胞。

中文摘要

γδ T 细胞被视为下一代癌症免疫治疗中有前景的效应淋巴细胞。尽管在人外周血中相对罕见,γδ T 细胞在上皮组织中更为丰富,而许多肿瘤正是在这些组织中发生,并已被证明作为细胞毒性细胞或“1 型”免疫协调者积极参与抗癌免疫。γδ T 细胞用于应对晚期癌症的一个主要优势是其不依赖于通过主要组织相容性复合体进行的抗原呈递,这使它们明显区别于传统的 αβ T 细胞。在此,我们讨论基于人 γδ T 细胞的主要治疗策略。这些策略包括基于抗体的双特异性衔接分子和过继性细胞疗法,分别聚焦于 Vδ1 + 或 Vδ2 + γδ T 细胞亚群,这些亚群可以被选择性扩增并分化或工程化改造,以最大化其抗肿瘤功能。我们综述支持每种正在开发的治疗策略的临床前数据;并总结为建立基于 γδ T 细胞的实体瘤和血液系统恶性肿瘤治疗而正在推进的临床试验。

展开英文摘要原文

γδ T cells are regarded as promising effector lymphocytes for next-generation cancer immunotherapies. In spite of being relatively rare in human peripheral blood, γδ T cells are more abundant in epithelial tissues where many tumors develop, and have been shown to actively participate in anticancer immunity as cytotoxic cells or as "type 1" immune orchestrators. A major asset of γδ T cells for tackling advanced cancers is their independence from antigen presentation via the major histocompatibility complex, which clearly sets them apart from conventional αβ T cells. Here we discuss the main therapeutic strategies based on human γδ T cells. These include antibody-based bispecific engagers and adoptive cell therapies, either focused on the Vδ1 + or Vδ2 + γδ T-cell subsets, which can be expanded selectively and differentiated or engineered to maximize their antitumor functions. We review the preclinical data that supports each of the therapeutic strategies under development; and summarize the clinical trials being pursued towards establishing γδ T cell-based treatments for solid and hematological malignancies.

论文信息

作者
Costa GP、Mensurado S、Silva-Santos B
第一作者单位
Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.Portugal
通讯作者单位
Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal sofiamensurado@medicina.ulisboa.pt bssantos@medicina.ulisboa.pt.Portugal
文献类型
综述 · 非美国政府资助研究
期刊
Journal for immunotherapy of cancer2023 Nov 24
原文标识
PubMed 38007241 · DOI 10.1136/jitc-2023-007955