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用于鉴定生物治疗药物免疫原性热点的 MAPPs;技术概述及其在生物制药领域的应用。

MAPPs for the identification of immunogenic hotspots of biotherapeutics; an overview of the technology and its application to the biopharmaceutical arena.

机构信息

a Department of BioAnalytical Sciences , Genentech Inc ., San Francisco , CA , USA.

b Department of Microchemistry , Proteomics & Lipidomics, Genentech Inc ., San Francisco , CA , USA.

出版信息

Expert Rev Proteomics. 2018 Sep;15(9):733-748. doi: 10.1080/14789450.2018.1521279. Epub 2018 Sep 17.

Abstract

Anti-drug antibody (ADA) responses are becoming an increasing concern as more highly engineered and sophisticated biotherapeutics enter the clinic. An arsenal of tools has been developed to identify potential T cell epitopes that may drive unwanted immunological responses to protein therapeutics; one such tool is termed 'Major Histocompatibility Complex-Associated Peptide Proteomics' (MAPPs). This review highlights the evolution of this MHC II profiling technology, its technological advantages and limitations, and its utility in helping to de-risk the immunogenicity of biotherapeutics. Areas covered: A comprehensive literature review was performed along with discussions with key leaders in the field of MAPPs to summarize the importance of monitoring potential immunogenicity of clinical molecules. Herein we also describe how MAPPs has been applied specifically for monitoring MHC II peptides derived from biotherapeutics. Expert commentary: Given the importance of this growing field we discuss the complementary tools used in conjunction with MAPPs and review case studies where this approach has informed clinical studies and in some cases allowed re-engineering of the biotherapeutic moiety to a less immunogenic format.

摘要

抗药物抗体(ADA)反应越来越受到关注,因为越来越多的高度工程化和复杂的生物疗法进入临床。已经开发了一系列工具来识别可能导致蛋白质治疗药物产生不良免疫反应的潜在 T 细胞表位;其中一种工具称为“主要组织相容性复合体相关肽蛋白质组学”(MAPPs)。本综述强调了这种 MHC II 分析技术的演变、其技术优势和局限性,以及它在帮助降低生物疗法免疫原性风险方面的应用。涵盖领域:进行了全面的文献综述,并与 MAPPs 领域的主要领导者进行了讨论,以总结监测临床分子潜在免疫原性的重要性。在此,我们还描述了 MAPPs 如何专门用于监测生物疗法衍生的 MHC II 肽。专家评论:鉴于这个不断发展的领域的重要性,我们讨论了与 MAPPs 一起使用的互补工具,并回顾了一些案例研究,其中这种方法为临床研究提供了信息,并在某些情况下允许对生物治疗部分进行重新设计,以降低其免疫原性。

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