免疫原性
抗体
肽
单克隆抗体
牛血清白蛋白
化学
抗原
肽库
分子生物学
病毒学
肽序列
生物化学
生物
免疫学
基因
作者
Yue Zhou,Jingzhi Li,W. Wu,Yanfei Chen,Cheng Hu,Mengyu Li,Yiyue Sun,Jiao Yang,Da-Xin Peng,Qinghong Xue,Hongwei Ma
标识
DOI:10.1093/intimm/dxac068
摘要
Abstract Immunogenicity can be evaluated by detecting antibodies (Abs) induced by an antigen. Presently deployed assays, however, do not consider the negative impacts of Ab poly-specificity, which is well established at the monoclonal antibody level. Here, we studied antibody poly-specificity at the serum level (i.e. nonspecific Ab–probe interactions, NSIs), and ended up establishing a new platform for viral peptide immunogenicity evaluation. We first selected three peptides of high, medium and low immunogenicity, using a ‘vaccine serum response rate’-based approach (i.e. the gold standard). These three peptides (Pi) in the bovine serum albumin–Pi form were used to immunize chickens, resulting in longitudinal serum samples for screening with a non-cognate peptide library. The signal intensity of Ab-peptide specific binding and ‘NSI count’ was used to evaluate the viral peptides’ immunogenicity. Only the NSI count agreed with the gold standard. The NSI count also provides more informative data on antibody production than the aggregated signal intensity by whole-protein-based indirect enzyme-linked immunosorbent assay.
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