Extraction and characterization of the rhesus macaque T-cell receptor β-chain genes

被引:14
作者
Greenaway, Hui Yee [1 ]
Kurniawan, Monica [1 ]
Price, David A. [2 ,3 ]
Douek, Daniel C. [3 ]
Davenport, Miles P. [1 ]
Venturi, Vanessa [1 ]
机构
[1] Univ New S Wales, Ctr Vasc Res, Complex Syst Biol Grp, Kensington, NSW 2052, Australia
[2] Cardiff Univ, Sch Med, Dept Med Biochem & Immunol, Cardiff, S Glam, Wales
[3] NIAID, Human Immunol Sect, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
基金
英国医学研究理事会; 美国国家卫生研究院; 澳大利亚研究理事会;
关键词
T-cell; T-cell receptor; T-cell receptor repertoire; SIMIAN IMMUNODEFICIENCY VIRUS; SIV INFECTION; ANIMAL-MODEL; REPERTOIRE DIVERSITY; IMMUNE-RESPONSE; INFLUENZA-VIRUS; TCR REPERTOIRE; CTL ESCAPE; CD8(+); MONKEYS;
D O I
10.1038/icb.2009.38
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rhesus macaque models have been instrumental in the development and testing of vaccines before human studies and have provided fundamental insights into the determinants of immune efficacy in a variety of infectious diseases. However, the characterization of antigen-specific T-cell receptor (TCR) repertoires during adaptive immune responses in these models has earlier relied on human TCR gene assignments. Here, we extracted and characterized TCR beta-chain (TRB) genes from the recently sequenced rhesus macaque genome that are homologous to the human TRB genes. Comparison of the rhesus macaque TRB genes with the human TRB genes showed an average best match similarity of 92.9%. Furthermore, we confirmed the usage of most rhesus macaque TRB genes by expressed TCR beta sequences within epitope-specific TCR repertoires. This primary description of the rhesus macaque TRB genes will provide a standardized nomenclature and enable better characterization of TCR usage in studies that use this species. Immunology and Cell Biology (2009) 87, 546-553; doi: 10.1038/icb.2009.38; published online 9 June 2009
引用
收藏
页码:546 / 553
页数:8
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