MONOCLONAL-ANTIBODIES RAISED AGAINST ENGINEERED SOLUBLE MOUSE T-CELL RECEPTORS AND SPECIFIC FOR V-ALPHA-8-BEARING, V-BETA-2-BEARING OR V-BETA-10-BEARING T-CELLS

被引:94
作者
NECKER, A
REBAI, N
MATTHES, M
JOUVINMARCHE, E
CAZENAVE, PA
SWARNWORAWONG, P
PALMER, E
MACDONALD, HR
MALISSEN, B [1 ]
机构
[1] CNRS MARSEILLE LUMINY,CTR IMMUNOL,INSERM,CASE 906,F-13288 MARSEILLE 09,FRANCE
[2] INST PASTEUR,F-75724 PARIS 15,FRANCE
[3] CNRS,UA 359,DEPT IMMUNOL,F-75005 PARIS,FRANCE
[4] NATL JEWISH CTR IMMUNOL & RESP MED,DIV BASIC SCI,DENVER,CO
[5] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT PEDIAT,DENVER,CO
[6] LUDWIG INST CANC RES,CH-1066 EPALINGES,SWITZERLAND
关键词
D O I
10.1002/eji.1830211220
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have characterized a panel of monoclonal antibodies (mAb) produced by immunizing rats with two distinct soluble mouse alpha/beta T cell receptor (TcR). Fifty mAb were found to react with the corresponding surface-bound TcR. Such observations suggest that the soluble TcR molecules used as immunogen are folded in a conformation similar to the native structure. Furthermore, the binding to T cells of four antibodies was found to correlate with the expression of the V-alpha-8, V-beta-2 or V-beta-10 gene segments. Finally, staining of T lymphocytes from various mouse strains suggests that (a) the two anti-V-alpha-8 antibodies recognize different epitopes, and each on only a fraction of V-alpha-8+ cells; (b) the anti-V-beta-10 mAb identifies a V-beta-10 polymorphism among mouse strains, and (c) T cells expressing the V-beta-2 or V-beta-10 gene segments are not subject to major clonal deletion events induced by the major histocompatibility complex class II and Mls products which were tested.
引用
收藏
页码:3035 / 3040
页数:6
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