单克隆抗体
T细胞受体
分子生物学
抗体
生物
T细胞
CD3型
受体
免疫原性
CD8型
白细胞介素2受体
转基因
抗原
免疫学
基因
免疫系统
生物化学
作者
Joanne L. Viney,Haydn M. Prosser,C R Hewitt,Jonathan R. Lamb,Michael J. Owen
出处
期刊:Hybridoma
[Mary Ann Liebert]
日期:1992-12-01
卷期号:11 (6): 701-713
被引量:32
标识
DOI:10.1089/hyb.1992.11.701
摘要
The generation of a panel of monoclonal antibodies specific for different variable (V) regions of human T cell receptors will be of great importance in the study of T cell-mediated diseases. However, relatively few such reagents exist, due in part to the poor immunogenicity of TcRs on the surface of human T cells. We have employed a strategy in which T cells from a transgenic mouse line expressing a human Vβ3Cβl TcR were used to immunise syngeneic conventional mice to generate two monoclonal antibodies specific for human T cell receptors. Binding of antibody JOVI.3, which stained approximately 5% of human peripheral blood CD3 positive T cells, correlated with the expression of the human TcR Vβ3 gene segment. Antibody JOVI·1 recognised a determinant on the majority of TcRs, staining 50-75% of peripheral blood T cells and T cell lines expressing different Vβ regions. Some TcRs, however, failed to react with this antibody. Both antibodies immunoprecipitated detergent-solubilised TcR molecules and were capable of inducing proliferation of peripheral blood T cells.
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