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Blood, 1 March 2007, Vol. 109, No. 5, pp. 2086-2088.
Prepublished online as a Blood First Edition Paper on October 19, 2006; DOI 10.1182/blood-2006-06-031385.


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Submitted June 27, 2006
Accepted October 13, 2006

Idiopathic CD4+ T lymphocytopenia is associated with increases in immature/transitional B cells and serum levels of IL-7

Angela Malaspina, Susan Moir*, Doreen G Chaitt, Catherine A Rehm, Shyam Kottilil, Judith Falloon, and Anthony S Fauci

National Institutes of Health, Department of Health and Human Services, United States

* Corresponding author; email: smoir{at}niaid.nih.gov.

Idiopathic CD4+ T lymphocytopenia (ICL) is a rare heterogeneous disorder defined by CD4+ T-cell counts below 300/µ1 in the absence of HIV infection or other known immune deficiency disorders. Here, we report the expansion of immature/transitional B cells in ICL patients that is associated with elevated serum levels of IL-7. Both the percentage of immature/transitional B cells and levels of IL-7 were inversely correlated with levels of CD4+ T cell counts and directly correlated to each other. Further analyses of B cells indicated that, in contrast to the activating effects of HIV disease on mature B cells, the expansion of immature/transitional B cells in ICL patients occurred at the expense of memory B cells. These findings extend previous reports on primary immunodeficiencies as well as HIV disease by suggesting that CD4+ T cell lymphopenia has an impact on human B cell development either directly or indirectly via the associated elevation of IL-7 levels.


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