Regulation of lupus-related autoantibody production and clinical disease by Toll-like receptors.

Abstract:

:Autoantigens that contain DNA, RNA, or self-IgG are preferred targets for autoantibodies in systemic lupus erythematosus (SLE). B cells promote SLE pathogenesis by producing autoantibodies, activating autoreactive T cells, and secreting cytokines. We discuss how certain autoreactive B cells are selectively activated, with emphasis on the roles of key Toll-like receptors (TLRs). Although TLR7, which recognizes ssRNA, promotes autoimmune disease, TLR9, which recognizes DNA, unexpectedly regulates disease, despite being required for the secretion of anti-chromatin autoantibodies. We describe positive feedback loops involving B cells, T cells, DCs, and soluble mediators, and how these networks are regulated by TLR signals.

journal_name

Semin Immunol

journal_title

Seminars in immunology

authors

Christensen SR,Shlomchik MJ

doi

10.1016/j.smim.2006.12.005

subject

Has Abstract

pub_date

2007-02-01 00:00:00

pages

11-23

issue

1

eissn

1044-5323

issn

1096-3618

pii

S1044-5323(06)00125-4

journal_volume

19

pub_type

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