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癌症免疫治疗中的共抑制途径。

Coinhibitory Pathways in Immunotherapy for Cancer.

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02215.

Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02215.

出版信息

Annu Rev Immunol. 2016 May 20;34:539-73. doi: 10.1146/annurev-immunol-032414-112049. Epub 2016 Feb 25.

Abstract

The immune system is capable of recognizing tumors and eliminates many early malignant cells. However, tumors evolve to evade immune attack, and the tumor microenvironment is immunosuppressive. Immune responses are regulated by a number of immunological checkpoints that promote protective immunity and maintain tolerance. T cell coinhibitory pathways restrict the strength and duration of immune responses, thereby limiting immune-mediated tissue damage, controlling resolution of inflammation, and maintaining tolerance to prevent autoimmunity. Tumors exploit these coinhibitory pathways to evade immune eradication. Blockade of the PD-1 and CTLA-4 checkpoints is proving to be an effective and durable cancer immunotherapy in a subset of patients with a variety of tumor types, and additional combinations are further improving response rates. In this review we discuss the immunoregulatory functions of coinhibitory pathways and their translation to effective immunotherapies for cancer.

摘要

免疫系统能够识别肿瘤并清除许多早期恶性细胞。然而,肿瘤会进化以逃避免疫攻击,肿瘤微环境具有免疫抑制性。免疫反应受许多免疫检查点的调节,这些检查点促进保护性免疫并维持耐受。T 细胞共抑制途径限制免疫反应的强度和持续时间,从而限制免疫介导的组织损伤,控制炎症的消退,并维持耐受以防止自身免疫。肿瘤利用这些共抑制途径来逃避免疫清除。阻断 PD-1 和 CTLA-4 检查点已被证明在多种肿瘤类型的一部分患者中是一种有效且持久的癌症免疫疗法,并且其他组合进一步提高了反应率。在这篇综述中,我们讨论了共抑制途径的免疫调节功能及其转化为有效的癌症免疫疗法。

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