Title of article
T cell epitope: Friend or Foe? Immunogenicity of biologics in context
Author/Authors
Weber، نويسنده , , Constanze A. and Mehta، نويسنده , , Preema J. and Ardito، نويسنده , , Matt and Moise، نويسنده , , Lenny and Martin، نويسنده , , Bill and De Groot، نويسنده , , Anne S.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
12
From page
965
To page
976
Abstract
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.
Keywords
T regulatory cells , TOLERANCE , MHC , Antigen , Anti-drug antibody , antibodies , Antigen presentation , immunoinformatics , T effector cells , T lymphocyte antigens
Journal title
Advanced Drug Delivery Reviews
Serial Year
2009
Journal title
Advanced Drug Delivery Reviews
Record number
1762710
Link To Document