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晚期HIV感染个体中未成熟/过渡性B细胞的出现:与白细胞介素-7升高的相关性

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

作者信息

Malaspina Angela, Moir Susan, Ho Jason, Wang Wei, Howell Melissa L, O'Shea Marie A, Roby Gregg A, Rehm Catherine A, Mican Joann M, Chun Tae-Wook, Fauci Anthony S

机构信息

Laboratory of Immunoregulation, and Office of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2262-7. doi: 10.1073/pnas.0511094103. Epub 2006 Feb 6.

Abstract

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.

摘要

HIV疾病的进展与众多B细胞缺陷的出现有关。我们在此描述了一群不成熟/过渡性B细胞,在HIV疾病进展的个体外周血中过度存在。这些通过CD10表达鉴定的B细胞,对B细胞受体触发的增殖无反应,具有证实其不成熟/过渡分化阶段的表型和Ig多样性谱。与不成熟状态一致,它们对B细胞受体触发缺乏增殖可被CD40配体逆转,但不能被B细胞活化因子逆转。最后,B细胞上CD10的表达水平与血清IL-7水平直接相关,表明IL-7水平升高通过对淋巴细胞减少的稳态作用直接或间接调节人类B细胞成熟。综上所述,这些数据为人类B细胞发育以及晚期HIV疾病中可能与IL-7依赖性稳态事件相关的B细胞功能障碍提供了见解。

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