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实体瘤的联合化学免疫疗法:改进疫苗?

Combined chemoimmunotherapy of solid tumours: improving vaccines?

作者信息

Nowak Anna K, Lake Richard A, Robinson Bruce W S

机构信息

Department of Medicine and Pharmacology, University of Western Australia, Sir Charles Gairdner Hospital, 4th Floor, G block, Sir Charles Gairdner Hospital, Hospital Avenue, Nedlands, WA 6009 Australia.

出版信息

Adv Drug Deliv Rev. 2006 Oct 1;58(8):975-90. doi: 10.1016/j.addr.2006.04.002. Epub 2006 Aug 15.

Abstract

Cytotoxic chemotherapy not only affects the tumour but also targets dividing lymphocytes, the very cells required to develop an immune response. Hence, chemo- and immunotherapy have been seen as antagonistic. It is now clear that the way a chemotherapeutic drug kills a tumour cell determines how that dying cell interacts with the immune system and whether the interaction leads to an immune response. Chemotherapy also depletes regulatory T cells, potentially enhancing immune responses. Furthermore, lymphodepletion triggers homeostatic T cell reconstitution, creating new populations of pre-T cells that need education in the thymic environment. Post-chemotherapy immune system reconstitution may provide a unique opportunity for therapeutic intervention by shaping the repertoire towards reactivity to tumour antigens. An understanding of the underlying cellular and immunological events in both animal models and patients undergoing chemotherapy will guide decisions about which immunomodulatory approaches may be effective with different cytostatic drugs and hence to develop appropriate scheduling for integration of the treatment modalities.

摘要

细胞毒性化疗不仅会影响肿瘤,还会靶向分裂中的淋巴细胞,而这些细胞正是产生免疫反应所必需的。因此,化疗和免疫疗法一直被视为相互拮抗的。现在很清楚,化疗药物杀死肿瘤细胞的方式决定了垂死细胞与免疫系统的相互作用方式,以及这种相互作用是否会引发免疫反应。化疗还会消耗调节性T细胞,从而有可能增强免疫反应。此外,淋巴细胞清除会触发稳态T细胞重建,产生需要在胸腺环境中接受“教育”的新的前体T细胞群体。化疗后免疫系统的重建可能为治疗干预提供独特的机会,通过塑造针对肿瘤抗原反应性的库。了解动物模型和接受化疗的患者体内潜在的细胞和免疫事件,将指导我们决定哪些免疫调节方法可能对不同的细胞抑制药物有效,从而制定合适的治疗方案整合时间表。

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