The idiotype connection: linking infection and multiple sclerosis

被引:8
作者
Holmoy, Trygve [1 ,2 ]
Vartdal, Frode [2 ]
Hestvik, Anne Lise [2 ]
Munthe, Ludvig [1 ,2 ]
Bogen, Bjarne [1 ,2 ]
机构
[1] Univ Oslo, Inst Immunol, Ctr Immune Regulat, Oslo, Norway
[2] Oslo Univ Hosp, Rikshosp, Oslo, Norway
关键词
CD4(+) T-CELLS; CENTRAL-NERVOUS-SYSTEM; IMMUNOGLOBULIN VARIABLE-REGION; 3RD HYPERVARIABLE REGION; AUTOREACTIVE B-CELLS; EPSTEIN-BARR-VIRUS; CEREBROSPINAL-FLUID; IMMUNE-RESPONSE; AUTOIMMUNE-DISEASE; MURINE LUPUS;
D O I
10.1016/j.it.2009.11.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cells present idiotopes (Id) from their B cell receptor to Id-specific CD4(+) T cells. Chronic Id-driven T-B cell collaboration can cause autoimmune disease in mice. We propose that Id-driven T-B cell collaboration mediates the development of multiple sclerosis by perpetuating immune responses initiated against infectious agents. During germinal centre reactions, B cells express a multitude of mutated Ids. While most mutations lead to decreased affinity and deletion of the B cell, some B cells could be rescued by Id-specific T cells. Such Id-connected T-B cell pairs might initiate inflammatory foci in the central nervous system. This model may explain the intrathecal synthesis of low-avidity IgG against viruses, and the synthesis of oligoclonal IgG with unknown specificity in multiple sclerosis.
引用
收藏
页码:56 / 62
页数:7
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