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程序性死亡配体 1

PD-L1.

机构信息

Departmentof Surgery and Cancer, Imperial College London, Hammersmith Hospital Campus, London, UK.

National Centre for HIV Malignancy, Chelsea and Westminster Hospital, London, UK.

出版信息

J Clin Pathol. 2018 Mar;71(3):189-194. doi: 10.1136/jclinpath-2017-204853. Epub 2017 Nov 2.

Abstract

Programmed death ligand 1 (PD-L1) is the principal ligand of programmed death 1 (PD-1), a coinhibitory receptor that can be constitutively expressed or induced in myeloid, lymphoid, normal epithelial cells and in cancer. Under physiological conditions, the PD-1/PD-L1 interaction is essential in the development of immune tolerance preventing excessive immune cell activity that can lead to tissue destruction and autoimmunity. PD-L1 expression is an immune evasion mechanism exploited by various malignancies and is generally associated with poorer prognosis. PD-L1 expression is also suggested as a predictive biomarker of response to anti-PD-1/PD-L1 therapies; however, contradictory evidence exists as to its role across histotypes. Over the years, anti-PD-1/PD-L1 agents have gained momentum as novel anticancer therapeutics, by inducing durable tumour regression in numerous malignancies including metastatic lung cancer, melanoma and many others. In this review, we discuss the immunobiology of PD-L1, with a particular focus on its clinical significance in malignancy.

摘要

程序性死亡配体 1(PD-L1)是程序性死亡 1(PD-1)的主要配体,PD-1 是一种共抑制受体,可在髓样细胞、淋巴样细胞、正常上皮细胞和癌症中组成性表达或诱导表达。在生理条件下,PD-1/PD-L1 相互作用对于免疫耐受的发展至关重要,可防止过度的免疫细胞活性导致组织破坏和自身免疫。PD-L1 表达是各种恶性肿瘤利用的免疫逃逸机制,通常与预后较差相关。PD-L1 表达也被认为是对抗 PD-1/PD-L1 治疗反应的预测性生物标志物;然而,其在不同组织类型中的作用存在矛盾的证据。多年来,抗 PD-1/PD-L1 药物作为新型抗癌治疗药物得到了发展,在包括转移性肺癌、黑色素瘤和许多其他肿瘤在内的多种恶性肿瘤中诱导了持久的肿瘤消退。在这篇综述中,我们讨论了 PD-L1 的免疫生物学,特别关注其在恶性肿瘤中的临床意义。

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