Changes in thymic function with age and during the treatment of HIV infection - PubMed (original) (raw)
. 1998 Dec 17;396(6712):690-5.
doi: 10.1038/25374.
R D McFarland, P H Keiser, E A Gage, J M Massey, B F Haynes, M A Polis, A T Haase, M B Feinberg, J L Sullivan, B D Jamieson, J A Zack, L J Picker, R A Koup
Affiliations
- PMID: 9872319
- DOI: 10.1038/25374
Changes in thymic function with age and during the treatment of HIV infection
D C Douek et al. Nature. 1998.
Abstract
The thymus represents the major site of the production and generation of T cells expressing alphabeta-type T-cell antigen receptors. Age-related involution may affect the ability of the thymus to reconstitute T cells expressing CD4 cell-surface antigens that are lost during HIV infection; this effect has been seen after chemotherapy and bone-marrow transplantation. Adult HIV-infected patients treated with highly active antiretroviral therapy (HAART) show a progressive increase in their number of naive CD4-positive T cells. These cells could arise through expansion of existing naive T cells in the periphery or through thymic production of new naive T cells. Here we quantify thymic output by measuring the excisional DNA products of TCR-gene rearrangement. We find that, although thymic function declines with age, substantial output is maintained into late adulthood. HIV infection leads to a decrease in thymic function that can be measured in the peripheral blood and lymphoid tissues. In adults treated with HAART, there is a rapid and sustained increase in thymic output in most subjects. These results indicate that the adult thymus can contribute to immune reconstitution following HAART.
Comment in
- The thymus in the age of retirement.
Rodewald HR. Rodewald HR. Nature. 1998 Dec 17;396(6712):630-1. doi: 10.1038/25251. Nature. 1998. PMID: 9872308 No abstract available.
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