Dysfunctional B cells in systemic lupus erythematosus.

Abstract:

:The classical view of B cells in the biology of autoimmune responses to infectious and self-antigens (Ag) that they promote immunity primarily by producing antibodies (Ab) is far from being complete. Indeed, studies over the last decade suggest that B cells have extraordinarily diverse functions within the immune system other than Ab production, which could contribute to autoimmunity. They normally play a role in the development of lymphoid architecture, regulating dentritic cells (DC) and T cell subsets function through cytokine production, and in activation of T cells. Receptor editing is also important in B cells which aids in immunity to infection and, possibly, prevention of autoimmunity. Both abnormalities in the distribution of B cells subsets and clinical benefit response to B cell depletion in autoimmune diseases, including systemic lupus erythematosus (SLE), highlight their pivotal function. Transgenic (Tg) animal models have shown that sensitivity of B cells to B cell Ag receptor (BCR) cross-linking is correlated to autoimmunity. Indeed, negative signaling by CD5 and other molecules, such as CD22, in maintaining tolerance through recruitment of src-homology two domain-containing protein tyrosine phosphatase-1 (SHP-1) has also been documented. In fact, we have now reached a newer area whereby B cells returned as an important contributor to autoimmune disorders.

journal_name

Autoimmun Rev

journal_title

Autoimmunity reviews

authors

Renaudineau Y,Pers JO,Bendaoud B,Jamin C,Youinou P

doi

10.1016/j.autrev.2004.07.035

keywords:

subject

Has Abstract

pub_date

2004-11-01 00:00:00

pages

516-23

issue

7-8

eissn

1568-9972

issn

1873-0183

pii

S1568-9972(04)00111-9

journal_volume

3

pub_type

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