4.7 Review

T cell epitope: Friend or Foe? Immunogenicity of biologics in context

期刊

ADVANCED DRUG DELIVERY REVIEWS
卷 61, 期 11, 页码 965-976

出版社

ELSEVIER
DOI: 10.1016/j.addr.2009.07.001

关键词

Antigen; MHC; Antibodies; Anti-drug antibody; Antigen presentation; Immunoinformatics; T lymphocyte antigens; T effector cells; T regulatory cells; Tolerance

向作者/读者索取更多资源

Like vaccines, biologic proteins can be very immunogenic for reasons including route of administration, dose frequency and the underlying antigenicity of the therapeutic protein. Because the impact of immunogenicity can be quite severe, regulatory agencies are developing risk-based guidelines for immunogenicity screening. T cell epitopes are at the root of the immunogenicity issue. Through their presentation to T cells, they activate the process of anti-drug antibody development Preclinical screening for T cell epitopes can be performed in silico, followed by in vitro and in vivo validation. Importantly, screening for immunogenicity is complicated by the discovery of regulatory T cell epitopes, which suggests that immunogenicity testing must now take regulatory T cells into consideration. In this review, we address the application of computational tools for preclinical immunogenicity assessment, the implication of the discovery of regulatory T cell epitopes, and experimental validation of those assessments. (C) 2009 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据