Etiopathogenesis of systemic lupus erythematosus: A 2014 update

被引:7
|
作者
Mathian, A. [1 ,2 ,3 ]
Arnaud, L. [1 ,2 ,3 ]
Amoura, Z. [1 ,2 ,3 ]
机构
[1] Grp Hosp Pitie Salpetriere, AP HP, Serv Med Interne 2, Ctr Natl Reference Lupus Syst & Syndrome Antiphol, F-75651 Paris, France
[2] Univ Paris 06, INSERM, UMR S 945, F-75013 Paris, France
[3] Univ Paris 06, F-75005 Paris, France
来源
REVUE DE MEDECINE INTERNE | 2014年 / 35卷 / 08期
关键词
Systemic lupus erythematosus; Etiopathogenesis; B-lymphocyte; alpha-interferon; BLys; PLASMACYTOID DENDRITIC CELLS; TOLL-LIKE RECEPTORS; ACTIVATE B-CELLS; I INTERFERON; ANTIPHOSPHOLIPID SYNDROME; IFN-ALPHA; EXPRESSION SIGNATURE; MEDIATED RESPONSE; IMMUNE-COMPLEXES; APOPTOTIC CELLS;
D O I
10.1016/j.revmed.2013.10.334
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Systemic lupus erythematous is a chronic autoimmune disease characterized by the inflammation of several tissues and the production of auto-antibodies directed against nuclear antigens. Complex genetic disorders and environmental factors are at the origin of the disease but the precise cause of the autoimmune process is still unknown. Both innate and adaptive immune systems are involved. Apoptosis seems to be the main source of auto-antigens. The interactions between apoptotic cells, dendritic cells and lymphocytes activate the production of pathogenic antibodies and T lymphocytes. Amplification loops sustain the auto-immune process and the chronic inflammation. Several data point out B-lymphocytes and several cytokines involved in their homeostasis as new promising therapeutic targets. (C) 2013 Societe nationale francaise de medecine interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:503 / 511
页数:9
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