Abstract
Failure of T-cell homeostasis is an important feature of HIV-1 infection. Substantial evidence indicates that T-cell homeostasis is independent of CD4+ and CD8+ subsets, and this may contribute to the decline of CD4+ T cells to low levels in this disease. Moreover, failure of T-cell homeostasis appears to precede the development of clinically-defined AIDS by approximately 1.5 to 2 years and is thus an important milestone in HIV-1 disease progression. We argue that T-cell turnover and depletion of memory cells in HIV-1 infection can be viewed as the reverse of the process by which immune reconstitution occurs after stem cell transplantation, and that changes in the functional level of T-cell memory may be critical to both processes. An understanding of the relationship between T-cell memory and regeneration of lost T cells may help preserve and/or reconstitute immune system homeostasis in HIV-1-infected individuals.
Original language | English (US) |
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Pages (from-to) | 381-388 |
Number of pages | 8 |
Journal | Seminars in immunology |
Volume | 9 |
Issue number | 6 |
DOIs | |
State | Published - Dec 1997 |
Keywords
- Apoptosis
- CD45
- Memory T cells
- Naive T cells
- Pronaive T cells
- T cell turnover
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology