Multiple sclerosis retrovirus particles and recombinant envelope trigger an abnormal immune response in vitro, by inducing polyclonal Vβ16 T-lymphocyte activation

被引:147
作者
Perron, H
Jouvin-Marche, E
Michel, M
Ounanian-Paraz, A
Camelo, S
Dumon, A
Jolivet-Reynaud, C
Marcel, F
Souillet, Y
Borel, E
Gebuhrer, L
Santoro, L
Marcel, S
Seigneurin, JM
Marche, PN
Lafon, M
机构
[1] Biomerieux Pierre Fabre, R&D, F-69280 Marcy Letoile, France
[2] Fac Med, Virol Lab, Grenoble, France
[3] INSERM, U238, F-38054 Grenoble, France
[4] Inst Pasteur, Unite Neurovirol & Regenerat Syst Nerveux, F-75724 Paris, France
[5] EFS, Lab Histocompatibil, F-69364 Lyon, France
[6] CHU A Michallon, Serv Neurol, F-38054 Grenoble, France
关键词
endogenous retrovirus; MSRV; HERV-W; envelope protein; immunopathology; T-lymphocyte; T-cell receptor; superantigen; cytokines; multiple sclerosis;
D O I
10.1006/viro.2001.1045
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A retroviral element (MSRV) defining a family of genetically inherited endogenous retroviruses (HERV-W) has recently been characterized in cell cultures from patients with multiple sclerosis (MS). To address the possible relationship with MS, direct detection of circulating virion RNA was proposed but revealed technically difficult to perform In standardized conditions, In the face of multiple endogenous HERV-W copies. A parallel approach has evaluated MSRV potential pathogenicity In relation to characteristic features of multiple sclerosis, in particular, T-lymphocyte-mediated immunopathology. We report here that MSRV particles Induce T-lymphocyte response with a bias in the V beta 16 chain usage in surface receptor, whatever the HLA DR of the donor. A recombinant MSRV envelope-but not core-protein reproduced similar nonconventional activation. Molecular analysis of V beta CDR3 showed that V beta 16 expansions are polyclonal. Our results thus provide evidence that MSRV envelope protein can trigger an abnormal immune response with similar characteristics to that of superantigens. (C) 2001 Academic Press.
引用
收藏
页码:321 / 332
页数:12
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