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

by: Angela Malaspina, Susan Moir, Jason Ho, Wei Wang, Melissa L. Howell, Marie A. O'Shea, Gregg A. Roby, Catherine A. Rehm, Joann M. Mican, Tae-Wook W. Chun, Anthony S. Fauci
Proceedings of the National Academy of Sciences of the United States of America, Vol. 103, No. 7. (14 February 2006), pp. 2262-2267, doi:10.1073/pnas.0511094103  Key: citeulike:10375242

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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.


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