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T Cell Development1


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* Education and Research Center and
National Liver Transplant Unit, St. Vincents University Hospital,
Dublin Institute of Technology, and
Conway Institute, University College Dublin, Dublin, Ireland; and
¶ Human Immunology Section and
|| Immunology Laboratory, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892
Normal adult human liver (AHL) contains populations of unconventional lymphocytes that have been shown in the mouse to mature locally. The presence of lymphoid progenitors together with IL-7, recombinase-activating gene, and pre-TCR-
expression in AHL suggests similar local T cell development activity in humans. Flow cytometry was used to characterize potentially naive hepatic 
-T cells. We looked for evidence of TCR-
cell development in AHL by quantifying
deletion TCR excision circles (TRECs) in CD3pos populations isolated from the liver and matched blood of eight individuals. Phenotypic analysis of hepatic T cells suggests the presence of Ag-inexperienced populations. TRECs were detected in all blood samples (mean, 164.10 TRECs/µg DNA), whereas only two hepatic samples were positive at low levels (59.40 and 1.92). The relatively high level of CD8pos T cells in these livers with a naive phenotype suggests that in addition to its role as a graveyard for Ag-specific activated CD8pos T cells, naive CD8pos T cells may enter the liver without prior activation. The almost complete absence of TRECs suggests that normal AHL is not a site for the development of conventional 
T cells.
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A. M. Williams, P. W. Bland, A. C. Phillips, S. Turner, T. Brooklyn, G. Shaya, R. D. Spicer, and C. S. J. Probert Intestinal {alpha}{beta} T Cells Differentiate and Rearrange Antigen Receptor Genes In Situ in the Human Infant J. Immunol., December 15, 2004; 173(12): 7190 - 7199. [Abstract] [Full Text] [PDF] |
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