HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Early HLA-B*57-restricted CD8+ T lymphocyte responses predict HIV-1 disease progression.

Abstract
Although HLA-B*57 (B57) is associated with slow progression to disease following HIV-1 infection, B57 heterozygotes display a wide spectrum of outcomes, including rapid progression, viremic slow progression, and elite control. Efforts to identify differences between B57-positive (B57(+)) slow progressors and B57(+) rapid progressors have largely focused on cytotoxic T lymphocyte (CTL) phenotypes and specificities during chronic stages of infection. Although CTL responses in the early months of infection are likely to be the most important for the long-term rate of HIV-1 disease progression, few data on the early CTL responses of eventual slow progressors have been available. Utilizing the Multicenter AIDS Cohort Study (MACS), we retrospectively examined the early HIV-1-specific CTL responses of 14 B57(+) individuals whose time to development of disease ranged from 3.5 years to longer than 25 years after infection. In general, a greater breadth of targeting of epitopes from structural proteins, especially Gag, as well as of highly conserved epitopes from any HIV-1 protein, correlated with longer times until disease. The single elite controller in the cohort was an outlier on several correlations of CTL targeting and time until disease, consistent with reports that elite control is typically not achieved solely by protective HLA-mediated CTLs. When targeting of individual epitopes was analyzed, we found that early CTL responses to the IW9 (ISPRTLNAW) epitope of Gag, while generally subdominant, correlated with delayed progression to disease. This is the first study to identify early CTL responses to IW9 as a correlate of protection in persons with HLA-B*57.
AuthorsCatherine A Brennan, F Javier Ibarrondo, Catherine A Sugar, Mary Ann Hausner, Roger Shih, Hwee L Ng, Roger Detels, Joseph B Margolick, Charles R Rinaldo, John Phair, Lisa P Jacobson, Otto O Yang, Beth D Jamieson
JournalJournal of virology (J Virol) Vol. 86 Issue 19 Pg. 10505-16 (Oct 2012) ISSN: 1098-5514 [Electronic] United States
PMID22811521 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Epitopes
  • HLA-B Antigens
  • HLA-B57 antigen
  • Peptides
  • gag Gene Products, Human Immunodeficiency Virus
Topics
  • Acquired Immunodeficiency Syndrome (blood)
  • CD8-Positive T-Lymphocytes (immunology, virology)
  • Cohort Studies
  • Disease Progression
  • Epitopes (chemistry)
  • Gene Expression Regulation, Viral
  • HIV-1 (metabolism)
  • HLA-B Antigens (genetics)
  • Humans
  • Male
  • Models, Statistical
  • Peptides (chemistry)
  • Phenotype
  • T-Lymphocytes, Cytotoxic (cytology)
  • gag Gene Products, Human Immunodeficiency Virus (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: