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Blood, 1 May 2005, Vol. 105, No. 9, pp. 3633-3640.
Prepublished online as a Blood First Edition Paper on January 11, 2005; DOI 10.1182/blood-2004-09-3740.
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Submitted October 7, 2004
Accepted December 27, 2004
B cell kinetics in humans: rapid turnover of peripheral blood memory cells
Derek C Macallan*, Diana L Wallace, Yan Zhang, Hala Ghattas, Becca Asquith, Catherine de Lara, Andrew Worth, George Panayiotakopoulos, George E Griffin, David F Tough, and Peter C Beverley
Department of Cellular and Molecular Medicine - Infectious Diseases, St George's Hospital Medical School, London, United Kingdom
Edward Jenner Institute for Vaccine Research, Compton, United Kingdom
Department of Immunology, Wright-Fleming Institute, Imperial College, London, United Kingdom
* Corresponding author; email: macallan{at}sghms.ac.uk.
Information about the kinetic behavior and lifespan of lymphocytes is crucial to understanding the mechanisms that regulate processes such as immunological memory. We have used in vivo labeling of dividing cells with 6,6-D2-glucose, combined with cell sorting and gas-chromatography-mass spectrometry for deuterium enrichment, in order to analyze the kinetics of human total, naive or memory B lymphocytes, separated from peripheral blood using monoclonal antibodies. We show that total blood B cells of young adults divide at an average rate of 1.9 ± 1.0 %/day and at a similar, though slightly slower rate, 1.5 ± 1.3 %/day, in the elderly. Separation of naive and memory B cells according to expression of CD27, indicates that naive peripheral blood B cells divide only slowly (0.46%/day), while memory cells proliferate more rapidly (2.66%/day). These data are compatible with the view that B cell memory may be maintained by clones of proliferating B cells.

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