University of Hawaii Cancer Center. He is an expert in the innate immunity and chronic inflammation-associated cancer fields.
University of Hawaii Cancer Center and studies the mechanisms of chronic inflammation-associated cancer.
Brief Funct Genomics. 2019 Mar 22;18(2):133-139. doi: 10.1093/bfgp/ely027.
Immune checkpoints have been the subject of a wave of new studies. Among these checkpoints are tytotoxic T-lymphocyte-associated antigen 4, checkpoints programmed death-1 and programmed death-ligand 1; their blockades have been approved by the Food and Drug Administration for therapy of melanoma and other types of cancers. Immunogenomics, which combines the latest nucleic acid sequencing strategy with immunotherapy, provides precise information about genomic alterations (e.g. mutations) and enables a paradigm shift of immune checkpoint therapy from tumor types to molecular signatures. Studying these critical checkpoints in relation to genomic mutations and neoantigens has produced groundbreaking results. This article examines these studies and delves into the relationships between immune checkpoint blockade and tumors harboring certain genomic mutations. Moreover, this article reviews recent studies on resistance to immune checkpoint therapy.
免疫检查点一直是一系列新研究的主题。这些检查点包括细胞毒性 T 淋巴细胞相关抗原 4、程序性死亡受体 1 和程序性死亡配体 1;它们的阻断作用已被美国食品和药物管理局批准用于治疗黑色素瘤和其他类型的癌症。免疫基因组学将最新的核酸测序策略与免疫疗法相结合,提供了关于基因组改变(如突变)的精确信息,并使免疫检查点治疗从肿瘤类型转变为分子特征成为可能。研究这些关键检查点与基因组突变和新抗原的关系已经产生了突破性的结果。本文研究了这些研究,并探讨了免疫检查点阻断与携带某些基因组突变的肿瘤之间的关系。此外,本文还回顾了最近关于免疫检查点治疗耐药性的研究。