表位
类毒素
外周血单个核细胞
破伤风
生物
毒素
免疫学
体外
T细胞
病毒学
免疫疗法
免疫原性
肽
免疫系统
抗体
接种疫苗
微生物学
生物化学
作者
Jeanette C. Reece,H. Mario Geysen,Stuart J. Rodda
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1993-12-01
卷期号:151 (11): 6175-6184
被引量:104
标识
DOI:10.4049/jimmunol.151.11.6175
摘要
Progress on the mapping of Th epitopes of tetanus toxin (tt) has been slow due to reliance on studies of clones. In this paper, human Th cell epitopes of tt were mapped using proliferation tests on PBMC in response to synthetic peptides. PBMC from nine donors were tested over the entire set of tt homologous overlapping dodecapeptides. The 1304 peptides were initially tested as 66 pools, each containing an average of 20 peptides. PBMC from individual donors responded to as few as 1 and as many as 17 of the 66 peptide pools. The sequences responsible for proliferation were identified for the two most frequently recognized pools, and for another two pools within a major immunodominant region. Three new epitope sequences were mapped in detail and based on their recognition by most individuals are likely to be promiscuous. A cocktail of peptides including the newly identified Th cell epitopes was able to induce proliferation in PBMC from 24 of 31 tetanus toxoid (TT)-responsive donors. This cocktail is a chemically defined reagent that can be used to quantitate in vitro Ag-specific Th cells in PBMC from most subjects, and may thus be useful for serial measurements of specific immunity such as in subjects undergoing immunotherapy or immunosuppressive treatment.
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