SELECTION OF T-CELL RECEPTOR VARIABLE GENE-ENCODED AMINO-ACIDS ON THE 3RD BINDING-SITE LOOP - A FACTOR INFLUENCING VARIABLE CHAIN SELECTION IN A T-CELL RESPONSE

被引:16
作者
CALLAN, MFC
REYBURN, HT
BOWNESS, P
ROWLANDJONES, S
BELL, JI
MCMICHAEL, AJ
机构
[1] Molecular Immunology Group, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford
基金
英国惠康基金;
关键词
T CELL RECEPTOR; CYTOTOXIC T LYMPHOCYTES; INFLUENZA;
D O I
10.1002/eji.1830250609
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The 3' end of the T cell receptor V beta 7.1 gene contains the five nucleotides CAAGA between the broadly conserved consensus sequence of nucleotides TGC/T GCC AGC AGC (which encode cysteine, alanine, serine and serine at positions 92-95 of the beta chain) and the heptamer that signals rearrangement. These nucleotides are frequently preserved during gene rearrangement, resulting in the common presence of glutamine at position 96 and of aspartate or glutamate at position 97 of the V beta 7.1 chain CDR3 loop in peripheral blood lymphocytes. There is selection of V beta 7.1 and of the V beta 7.1 gene-encoded glutamate at position 97 of the beta chain CDR3 loop in the cytotoxic T lymphocyte response to the HLA B2705-restricted influenza A nucleoprotein epitope SRYWAIRTR. Our results indicate that selection of V beta 7.1 gene-encoded amino acid residues on CDR3 loops may be one factor driving selection of V beta 7.1 in this response.
引用
收藏
页码:1529 / 1534
页数:6
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