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Recombination-mediated Escape from Primary CD8+ T Cells in Acute HIV-1 Infection

Overview
Journal Retrovirology
Publisher Biomed Central
Specialty Microbiology
Date 2014 Sep 13
PMID 25212771
Citations 22
Authors
Affiliations
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Abstract

Background: 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.

Results: 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.

Conclusions: 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.

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Identification of the Near Full-Length Genome of a Novel HIV-1 CRF01_AE/CRF07_BC Recombinant in Hebei Province, China.

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Elevated HIV viral load is associated with higher recombination rate .

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PMID: 37873119 PMC: 10592651. DOI: 10.1101/2023.05.05.539643.


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