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Journal of Experimental Medicine, Vol 184, 1083-1091, Copyright © 1996 by Rockefeller University Press
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B Zheng, S Han and G Kelsoe
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore 21201-1559, USA.
After immunization, activated splenic T cells proliferate in periarteriolar lymphoid sheaths (PALS) and subsequently migrate to the lymphoid follicle where they enter nascent germinal centers. Analysis of TCR V(D)J gene rearrangements indicates extensive emigration, frequently involving more than a single white pulp region. These migrants constitute a unique set of T helper cells that express antigen- specific alpha beta TCR, CD3, and CD4, but little or no Thy-1, a differentiation antigen present on the great majority of peripheral murine T lymphocytes. The origin of CD4+ Thy-1 follicular T cells appears to be the Thy+ population in the PALS, as both sets commonly share identical V(D)J rearrangements.
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