Abnormalities of B cell subsets in patients with systemic lupus erythematosus

被引:114
作者
Doerner, Thomas [1 ,2 ]
Jacobi, Annett M. [3 ]
Lee, Jisoo [4 ]
Lipsky, Peter E. [5 ]
机构
[1] Charite Univ Med Berlin, Dept Med Rheumatol & Clin Immunol, D-10098 Berlin, Germany
[2] Deutsch Rheumaforschungszentrum, D-10098 Berlin, Germany
[3] Univ Munster, Dept Med, D-4400 Munster, Germany
[4] Ewha Womans Univ, Sch Med, Dept Internal Med, Div Rheumatol, Seoul, South Korea
[5] NIAMS, NIH, Bethesda, MD USA
关键词
B cells; Phenotyping; Systemic lupus erythematosus; Plasma cells;
D O I
10.1016/j.jim.2010.06.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The prototypic autoimmune disease, SLE, is known to be associated with polyclonal B cell hyperreactivity. Developing an understanding of the complex nature of human B cell differentiation, largely through the application of multiparameter flow cytometry to an analysis of circulating B cells has permitted an assessment of whether specific stages of B cell maturation are affected by the tendency for polyclonal B cell activation. Moreover, the analysis of perturbations of the specific stages of B cell maturation has generated new information on whether abnormalities in B cell differentiation are primarily involved in autoimmune disease immunopathology or, rather, are secondary to the inflammatory environment characteristic of subjects with this autoimmune disease. Multivariant analysis has begun to document abnormalities in B cell maturation that are primarily associated with lupus, or, alternatively related to disease duration, disease activity and concomitant medication. Together, these analyses have provided new insights on the role of B cell over-reactivity in SLE. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
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