Evolution of studies of HLA class I antigen processing machinery (APM) components in malignant cells.

Clinical transplants Pub Date : 2013-01-01
Francesco Sabbatino, Joseph H Schwab, Soldano Ferrone, Cristina R Ferrone
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Abstract

Following a description of the way studies of human leukocyte antigen (HLA) class I antigen expression by tumor cells have evolved through the years, the literature related to the frequency of defects in HLA class I antigen processing machinery (APM) component expression in various types of malignancies is reviewed. In addition, the clinical significance of defects in HLA class I APM components as well as the underlying molecular mechanisms are described. Lastly, potential strategies to overcome the defects in HLAclass I APM component expression and function are discussed. The information presented indicates a revival of the interest in the characterization of HLA class I APM component expression by tumor cells since these molecules may play an important role in the outcome of immunotherapy with inhibitory checkpoint molecule-specific monoclonal antibodies in patients with malignant disease. Furthermore, they may represent a useful prognostic biomarker to select patients who might benefit from these types of immunotherapy.

恶性细胞HLA I类抗原加工机制(APM)成分的研究进展。
在介绍了多年来肿瘤细胞对人类白细胞抗原(HLA) I类抗原表达的研究进展之后,本文对不同类型恶性肿瘤中HLA I类抗原加工机械(APM)成分表达缺陷频率的相关文献进行了综述。此外,本文还描述了HLA I类APM成分缺陷的临床意义及其潜在的分子机制。最后,讨论了克服HLAclass I APM组件表达和功能缺陷的潜在策略。这些信息表明,肿瘤细胞中HLA I类APM成分表达的表征重新引起了人们的兴趣,因为这些分子可能在恶性疾病患者使用抑制性检查点分子特异性单克隆抗体进行免疫治疗的结果中发挥重要作用。此外,它们可能代表一种有用的预后生物标志物,以选择可能从这些类型的免疫治疗中受益的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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