Sign In
CAVD Portal Log On
Log On Help
search
Home
The CAVD
The Research
The Grantees
About the CAVD
CAVD Structure
Collaborating Institutions
History of the CAVD
Legal Agreements
Young Investigators Recognition
About the Research
Progress in the CAVD
Publications
Conference Abstracts
Study Results
Gallo Vaccine Discovery Consortium
Greenberg Mouse Immunology Lab
Haynes Vaccine Discovery Consortium
Haynes Centralized Envelope Development Consortium
Ho Vaccine Discovery Consortium
Ho Ibalizumab Development Consortium
Koup Vaccine Immune Monitoring Consortium
Letvin Vaccine Discovery Consortium
McElrath Vaccine Discovery Consortium
Montefiori Vaccine Immune Monitoring Consortium
Pantaleo Vaccine Discovery Consortium
Pantaleo Poxvirus Vaccine Development Consortium
Parks Vaccine Discovery Consortium
Patterson Vaccine Discovery Consortium
Reinherz Vaccine Discovery Consortium
Self Vaccine Immunology Statistical Center
Stamatatos Vaccine Discovery Consortium
von Briesen HIV Specimen Cryorepository
Walker Vaccine Discovery Consortium
Weiss Vaccine Discovery Consortium
Wilson Vaccine Discovery Consortium
Zolla-Pazner Vaccine Discovery Consortium
Title
Role of human immunodeficiency virus (HIV)-specific T-cell immunity in control of dual HIV-1 and HIV-2 infection
Primary Author
Zheng, NN
Authors
Zheng NN, McElrath MJ, Sow PS, Hawes SE, Diallo-Agne H, Stern JE, Li F, Mesher AL, Robinson AD, Gottlieb GS, Huang Y, Kiviat NB.
CAVD Grantee
Koup VIMC
Journal Name
Journal of Virology
Publication Date
9/1/2007
PubMed Search
Find in PubMed
Link to full-text
PMID
17582003
Abstract
Progressive immune dysfunction and AIDS develop in most cases of human immunodeficiency virus type 1 (HIV-1) infection but in only 25 to 30% of persons with HIV-2 infection. However, the natural history and immunologic responses of individuals with dual HIV-1 and HIV-2 infection are largely undefined. Based on our previous findings, we hypothesized that among patients with dual infection the control of HIV-1 is associated with the ability to respond to HIV-2 Gag epitopes and to maintain HIV-specific CD4(+) T-cell responses. To test this, we compared the HIV-specific ex vivo IFN-gamma enzyme-linked immunospot (ELISPOT) assay responses of 19 dually infected individuals to those of persons infected with HIV-1 or HIV-2 only. Further, we assessed the functional profile of HIV Gag-specific CD4(+) and CD8(+) T cells from nine HIV dually infected patients by using a multicolor intracellular cytokine staining assay. As determined by ELISPOT assay, the magnitude and frequency of IFN-gamma-secreting T-cell responses to gene products of HIV-1 were higher than those to gene products of HIV-2 (2.64 versus 1.53 log(10) IFN-gamma spot-forming cells/10(6) cells [90% versus 63%, respectively].) Further, HIV-1 Env-, Gag-, and Nef- and HIV-2 Gag-specific responses were common; HIV-2 Nef-specific responses were rare. HIV-specific CD4(+) T helper responses were detected in nine of nine dually infected subjects, with the majority of these T cells producing gamma interferon (IFN-gamma) and tumor necrosis factor alpha (TNF-alpha) and, to a lesser extent, interleukin-2. The HIV-1 plasma viral load was inversely correlated with HIV-2 Gag-specific IFN-gamma-/TNF-alpha-secreting CD4(+) and HIV-2 Gag-specific IFN-gamma-secreting CD8(+) T cells. In conclusion, the T-cell memory responses associated with containment of single HIV-1 and HIV-2 infection play a similar significant role in the immune control of dual HIV-1 and HIV-2 infection.
Was this publication authored by individuals from more than one CAVD Consortium?
No
Collaborating Consortia
Attachments
Created at 3/16/2009 11:53 AM by Hilda Villavicencio
Last modified at 3/16/2009 11:53 AM by Hilda Villavicencio
Use this page to add attachments to an item.
Name
© CAVD
Non-Member Access