Recombination-mediated escape from primary CD8+ T cells in acute HIV-1 infection
- University of Oxford (United Kingdom); DOE/OSTI
- Duke University, Durham, NC (United States)
- University of Oxford (United Kingdom)
- University of KwaZulu-Natal, Durban (South Africa)
- Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Santa Fe Institute. (SFI), Santa Fe, NM (United States)
- Duke University, Durham, NC (United States); Jilin University, Changchun (China
- University of North Carolina, Chapel Hill, NC (United States)
A major immune evasion mechanism of HIV-1 is the accumulation of non-synonymous mutations in and around T cell epitopes, resulting in loss of T cell recognition and virus escape. Here we analyze primary CD8+ T cell responses and virus escape in a HLA B*81 expressing subject who was infected with two T/F viruses from a single donor. In addition to classic escape through non-synonymous mutation/s, we also observed rapid selection of multiple recombinant viruses that conferred escape from T cells specific for two epitopes in Nef. Our study shows that recombination between multiple T/F viruses provide greater options for acute escape from CD8+ T cell responses than seen in cases of single T/F virus infection. This process may contribute to the rapid disease progression in patients infected by multiple T/F viruses.
- Research Organization:
- Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Biological and Environmental Research (BER). National Institutes of Health (NIH)
- Grant/Contract Number:
- AC52-06NA25396
- OSTI ID:
- 1626906
- Journal Information:
- Retrovirology, Journal Name: Retrovirology Journal Issue: 1 Vol. 11; ISSN 1742-4690
- Publisher:
- BioMed CentralCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Similar Records
Rapid selection of escape mutants by the first CD8 T cell responses in acute HIV-1 infection
Transmitted virus fitness and host T cell responses collectively define divergent infection outcomes in two HIV-1 recipients
Quantifying factors determining the rate of CTL escape and reversion during acute and chronic phases of HIV infection
Journal Article
·
Mon Dec 31 23:00:00 EST 2007
· Nature Immunology
·
OSTI ID:960875
Transmitted virus fitness and host T cell responses collectively define divergent infection outcomes in two HIV-1 recipients
Journal Article
·
Wed Jan 07 19:00:00 EST 2015
· PLoS Pathogens
·
OSTI ID:1201431
Quantifying factors determining the rate of CTL escape and reversion during acute and chronic phases of HIV infection
Journal Article
·
Wed Dec 31 23:00:00 EST 2008
· Journal of Virology
·
OSTI ID:970581