Identification and Characterization of a Human CD5+ Pre-Naive B Cell Population

被引:111
作者
Lee, Jisoo [1 ,2 ]
Kuchen, Stefan [1 ]
Fischer, Randy [1 ]
Chang, Sooghee [3 ]
Lipsky, Peter E. [1 ]
机构
[1] NIAMSD, Autoimmun Branch, NIH, Bethesda, MD 20892 USA
[2] Ewha Womans Univ, Sch Med, Div Rheumatol, Dept Internal Med, Seoul, South Korea
[3] Catholic Univ, Coll Med, Rheumatism Res Ctr, Seoul, South Korea
基金
美国国家卫生研究院;
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; LYMPHOCYTE SUBSETS; RHEUMATOID-FACTOR; PLASMA-CELLS; ANTIBODY; SELECTION; BLOOD; SIGNALS; RECONSTITUTION; COMPARTMENT;
D O I
10.4049/jimmunol.0803391
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have identified a distinct pre-naive B cell population circulating in human peripheral blood that exhibits an intermediate phenotype between transitional and naive B cells. Like human transitional B cells, these cells express CD5 but have intermediate densities of CD38, CD10, CD9, and the ABCB1 transporter compared with transitional and naive B cells. These pre-naive B cells account for a majority of circulating human CD5(+) B cells. Importantly, CD5(+) pre-naive B cells could be induced to differentiate into cells with a naive phenotype in vitro. CD5(+) pre-naive B cells show only partial responses to BCR stimulation and CD40 ligation and undergo more spontaneous apoptosis and cell death than do naive B cells, whereas BAFF/BLyS (B cell-activating factor belonging to the TNF family) did not enhance their survival compared with naive B cells. In contrast, CD5+ pre-naive B cells carry out certain functions comparable to naive B cells, including the capacity to differentiate into plasma cells and the ability to function as APCs. Notably, an increased proportion of CD5+ pre-naive B cells were found in peripheral blood of patients with systemic lupus erythematosus. These results have identified a unique intermediate in human naive B cell development within the peripheral blood and derangements of its homeostasis in patients with systemic lupus erythematosus. The Journal of Immunology, 2009, 182: 4116-4126.
引用
收藏
页码:4116 / 4126
页数:11
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