摘要
免疫治疗的目的是通过激活针对多种肿瘤新抗原的淋巴细胞反应来增强抗癌免疫应答。为了获得有效的免疫反应,解释学方法要求通过一些免疫检查点,例如激活兴奋性共刺激信号或避免协同抑制分子。在IMMUN中膜结合配体pd-1与其受体pd-L1的相互作用在众多临床试验中得到了广泛的关注。包括非小细胞肺癌(NSCLC)。然而,这些治疗药物作为单药治疗存在一些局限性,只有30 - 40%的患者观察到客观反应,大多数病人表现出先天抵抗力,大约25%的应答者后来显示疾病进展。肿瘤免疫研究的最新进展Y在人体样本中的翻译研究中有潜力识别先天和后天对免疫检查点抑制剂的抵抗力机制。本文主要对生物基础进行综述。免疫检查点阻断的IC原理,并着重介绍NSCLC患者免疫检查点阻断的现状和前景。
关键词: 非小细胞肺癌,免疫治疗,免疫监视,免疫逃避,PD-1,PD-L1。
Current Molecular Medicine
Title:Immunotherapy in Non-Small Cell Lung Cancer: Biological Principles and Future Opportunities
Volume: 17 Issue: 8
关键词: 非小细胞肺癌,免疫治疗,免疫监视,免疫逃避,PD-1,PD-L1。
摘要: Immunotherapy aims to amplify the anticancer immune response through reactivation of the lymphocytic response raised against several tumor neo-antigens. To obtain an effective immune response, this therapeutic approach requires that a number of immunological checkpoints be passed, such as the activation of excitatory costimulatory signals or the avoidance of coinhibitory molecules. Among the immune checkpoints, the interaction of the membrane-bound ligand PD-1 and its receptor PD-L1 has received much attention because of remarkable efficacy in numerous clinical trials for various cancer types, including non-small cell lung cancer (NSCLC). However, several limitations exist with these therapeutic agents when used as monotherapy, with objective responses observed in only 30–40% of patients, with the majority of patients demonstrating innate resistance, and approximately 25% of responders later demonstrating disease progression. Recent developments in the understanding of cancer immunology have the potential to identify mechanisms of innate and acquired resistance to immune checkpoint inhibitors through translational research in human samples. This review focuses on the biological basic principles for immunological checkpoint blockade, and highlights the current status and the perspectives of this therapeutic approach in NSCLC patients.
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Immunotherapy in Non-Small Cell Lung Cancer: Biological Principles and Future Opportunities, Current Molecular Medicine 2017; 17 (8) . https://dx.doi.org/10.2174/1566524018666180222114038
DOI https://dx.doi.org/10.2174/1566524018666180222114038 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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