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实体瘤的过继性T细胞疗法:是时候与免疫原性化疗/放疗联合应用了。

Adoptive T cell therapy of solid tumors: time to team up with immunogenic chemo/radiotherapy.

作者信息

Pocaterra Arianna, Catucci Marco, Mondino Anna

机构信息

Lymphocyte Activation Unit, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Via Olgettina, 58, 20132, Milan, Italy.

Lymphocyte Activation Unit, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Via Olgettina, 58, 20132, Milan, Italy.

出版信息

Curr Opin Immunol. 2022 Feb;74:53-59. doi: 10.1016/j.coi.2021.10.004. Epub 2021 Nov 4.

DOI:10.1016/j.coi.2021.10.004
PMID:34743069
Abstract

Adoptive T cell therapy (ACT) with tumor-reactive lymphocytes can overcome the immune desert of poorly immunogenic tumors and instruct tumor eradication. Several hurdles limit the efficacy of this strategy against solid tumor including, but not limited to, sub optimal T cell engraftment, tumor infiltration, poor tumor antigenicity/immunogenicity, and immunosuppressive or resistance mechanisms. Recent advances indicate that concomitant treatments can be set in place to offset such barriers. In this review, we highlight the beneficial effects of combining ACT with conventional chemo and/or radiotherapy. While originally classified as immunosuppressive, these methodologies can also promote the engraftment of ACT products, immunogenic cell death, and the reprogramming of more favorable microenvironments. Data indicates that systemic and local chemo/radiotherapy regimens promote intratumoral cytokine and chemokine upregulation, tumor antigen presentation and cross presentation, infiltration and in situ T cells reactivation. Here we review the most recent contributions supporting these notions and discuss further developments.

摘要

采用肿瘤反应性淋巴细胞进行过继性T细胞疗法(ACT)可克服免疫原性较差肿瘤的免疫逃逸并实现肿瘤清除。该策略针对实体瘤的疗效受到多个障碍的限制,包括但不限于次优的T细胞植入、肿瘤浸润、较差的肿瘤抗原性/免疫原性以及免疫抑制或抵抗机制。最新进展表明,可以采用联合治疗来克服这些障碍。在本综述中,我们重点介绍了ACT与传统化疗和/或放疗联合使用的有益效果。虽然这些方法最初被归类为免疫抑制,但它们也可以促进ACT产品的植入、免疫原性细胞死亡以及更有利微环境的重编程。数据表明,全身和局部化疗/放疗方案可促进肿瘤内细胞因子和趋化因子上调、肿瘤抗原呈递和交叉呈递、浸润以及原位T细胞再激活。在此,我们综述支持这些观点的最新研究成果并讨论进一步的发展。

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