Appearance of immature/transitional B cells in HIV-infected individuals with advanced disease: Correlation with increased IL-7

被引:171
作者
Malaspina, A
Moir, S
Ho, J
Wang, W
Howell, ML
O'Shea, MA
Roby, GA
Rehm, CA
Mican, JM
Chun, TW
Fauci, AS
机构
[1] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Off Clin Res, NIH, Bethesda, MD 20892 USA
关键词
immunopathogenesis; CD10; CD21; B cell receptor; lymphopenia;
D O I
10.1073/pnas.0511094103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Progression of HIV disease is associated with the appearance of numerous B cell defects. We describe herein a population of immature/transitional B cells that is overly represented in the peripheral blood of individuals with advancing HIV disease. These B cells, identified by the expression of CD10, were unresponsive by proliferation to B cell receptor triggering and possessed a phenotype and an Ig diversity profile that confirmed their immature/transitional stage of differentiation. Consistent with an immature status, their lack of proliferation to B cell receptor triggering was reversed with CD40 ligand, but not B cell activation factor. Finally, levels of CD10 expression on B cells were directly correlated with serum levels of IL-7, suggesting that increased levels of IL-7 modulate human B cell maturation either directly or indirectly by means of a homeostatic effect on lymphopenia. Taken together, these data offer insight into human B cell development as well as B cell dysfunction in advanced HIV disease that may be linked to IL-7-dependent homeostatic events.
引用
收藏
页码:2262 / 2267
页数:6
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