Abstract |
Recently HIV-infected individuals have virus-specific responses characterized by IFN-gamma/IL-2 secretion and proliferation rarely seen in chronic infection. To investigate the timing of loss of HIV-specific T-cell function, we screened cells from 59 treatment-naïve HIV-infected individuals with known dates of infection for proteome-wide responses secreting IFN-gamma/IL-2 and IFN-gamma alone by ELISPOT. HIV peptide-specific proliferation was assessed by carboxyfluorescein diacetate succinimidyl ester ( CFSE) dilution. The contribution of IFN-gamma/IL-2 and IFN-gamma-only secretion to the total HIV-specific response was compared in subjects infected <6, 6-12, and 12-36 mo earlier. The frequency of IFN-gamma/IL-2-secreting cells fell, while that of IFN-gamma-only secretion rose with time from infection. HIV peptide-specific proliferative responses were almost exclusively mediated by CD8(+) T cells, and were significantly lower in cells obtained from the 12-36 mo versus < 6 mo post- infection groups. By the second year of infection there was a significant difference in these functions compared to those assessed within 6 mo.
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Authors | Michel L Ndongala, Philomena Kamya, Salix Boulet, Yoav Peretz, Danielle Rouleau, Cécile Tremblay, Roger Leblanc, Pierre Côté, Jean-Guy Baril, RéJean Thomas, Sylvie Vézina, Mohamed R Boulassel, Jean-Pierre Routy, Rafick P Sékaly, Nicole F Bernard |
Journal | Viral immunology
(Viral Immunol)
Vol. 23
Issue 2
Pg. 159-68
(Apr 2010)
ISSN: 1557-8976 [Electronic] United States |
PMID | 20373996
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Human Immunodeficiency Virus Proteins
- Interleukin-2
- Peptides
- Proteome
- Interferon-gamma
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Topics |
- Adult
- CD8-Positive T-Lymphocytes
(immunology, metabolism)
- Female
- HIV Infections
(immunology)
- HIV-1
(immunology)
- Human Immunodeficiency Virus Proteins
(immunology)
- Humans
- Interferon-gamma
(biosynthesis)
- Interleukin-2
(biosynthesis)
- Lymphocyte Count
- Male
- Peptides
(immunology)
- Proteome
- T-Cell Antigen Receptor Specificity
- T-Lymphocytes
(immunology, metabolism)
- Time Factors
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