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Phylogenetic analysis of HIV-1 archived DNA in blood and gut-associated lymphoid tissue in two patients under antiretroviral therapy.

Authors :
Recordon-Pinson, Patricia
Gosselin, Annie
Ancuta, Petronela
Routy, Jean-Pierre
Fleury, Hervé
Source :
Gut Pathogens. 3/23/2021, Vol. 13 Issue 1, p1-6. 6p.
Publication Year :
2021

Abstract

One of the approaches to cure human immunodeficiency virus (HIV) is the use of therapeutic vaccination. We have launched the Provir/Latitude 45 study to identify conserved CTL epitopes in archived HIV-1 DNA according to the HLA class I alleles in aviremic patients under antiretroviral therapy (ART). A HIV-1 polypeptidic therapeutic vaccine based on viral sequence data obtained from circulating blood was proposed; here, our aim was to compare the proviral DNA in blood and gut-associated lymphoid tissue (GALT). Peripheral blood mononuclear cells and gut biopsies were obtained from two HIV-1 infected patients under successful antiretroviral therapy. Total DNA was extracted including the proviral DNA. The HIV-1 reverse transcriptase was sequenced in both compartments using next generation sequencing followed by single genome sequencing; phylogenetic trees were established and compared. The proviral sequences of both compartments intra-patient exhibited a very low genetic divergence while it was possible to differentiate the sequences inter-patients; single genome sequencing analysis of two couples of samples confirmed that there was no compartmentalization of the sequences intra-patient. We conclude that, considering these two cases, the proviral DNA sequences in blood and GALT are similar and that the epitope analysis of HIV-1 provirus in blood should be considered as relevant to that observed in the GALT, a hard-to-reach major compartment, and can therefore be used for therapeutic vaccine approaches. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17574749
Volume :
13
Issue :
1
Database :
Academic Search Index
Journal :
Gut Pathogens
Publication Type :
Academic Journal
Accession number :
149433416
Full Text :
https://doi.org/10.1186/s13099-021-00416-6