Immunovirological discordance among female sex workers who start antiretroviral therapy in Burkina Faso.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
03 Feb 2022
Historique:
received: 19 09 2021
accepted: 31 01 2022
entrez: 4 2 2022
pubmed: 5 2 2022
medline: 8 2 2022
Statut: epublish

Résumé

In people living with HIV/AIDS (PLWHA), initiation of antiretroviral therapy (ART) leads to sustained effective suppression of viral replication and increasing CD4 + T cell count. However, a fraction of ART-treated patients still fail to reach adequate CD4 + T cell number despite a suppressed viral load (VL), and this phenomenon is defined as immunovirological discordance (IVD). In Africa, several studies have reported immunovirological outcomes of antiretroviral therapy, but little is known about IVD occurrence in Female sex workers (FSW). This study aimed to assess the prevalence of IVD and associated factors among a cohort of HIV infected FSW in Burkina Faso. We conducted a cohort study from December 2003 to October 2016. Immunovirological discordance was defined as CD4 + T cell gain < 100 cells/µL despite a suppressed VL (VL < 1000 copies/mL) 12 months after ART initiation. The CD4 + T cells were counted using BD FACSCount™ System and point of care Pima™ CD4 + Analyzer. HIV-1 RNA was quantified by real-time polymerase-chain-reaction assay with the use of the ABI 7000 system. We conducted a logistic regression to identify factors associated with discordant responses. Among the 123 HIV-1 infected FSW having at least 12 months follow-up on ART, 105 (85.4%) achieved HIV-1 RNA suppression. Among the latter 25 gained less than 100 CD4 + T cells within 12 months follow-up. The IVD rate was 23.8% (95%CI 16.04%-33.11%). After adjustment for age, WHO clinical stage and ART regimen including nucleoside/nucleotide reverse transcriptase inhibitors, only baseline CD4 + T cell count between 200 to 350 cells/µL (adjusted OR: 4.15; 95%CI 1.13-15.22) and 350 to 500 cells/µL (adjusted OR: 17.50; 95%CI 2.68-114.31) remain significantly associated with IVD occurrence. Immunovirological discordance response was common in FSW with proportions close to those observed in the general population. A diagnosis and personalized follow-up of patients who do not achieve full immune reconstitution would make it possible to avoid complications in terms of morbidity and mortality.

Sections du résumé

BACKGROUND BACKGROUND
In people living with HIV/AIDS (PLWHA), initiation of antiretroviral therapy (ART) leads to sustained effective suppression of viral replication and increasing CD4 + T cell count. However, a fraction of ART-treated patients still fail to reach adequate CD4 + T cell number despite a suppressed viral load (VL), and this phenomenon is defined as immunovirological discordance (IVD). In Africa, several studies have reported immunovirological outcomes of antiretroviral therapy, but little is known about IVD occurrence in Female sex workers (FSW). This study aimed to assess the prevalence of IVD and associated factors among a cohort of HIV infected FSW in Burkina Faso.
METHODS METHODS
We conducted a cohort study from December 2003 to October 2016. Immunovirological discordance was defined as CD4 + T cell gain < 100 cells/µL despite a suppressed VL (VL < 1000 copies/mL) 12 months after ART initiation. The CD4 + T cells were counted using BD FACSCount™ System and point of care Pima™ CD4 + Analyzer. HIV-1 RNA was quantified by real-time polymerase-chain-reaction assay with the use of the ABI 7000 system. We conducted a logistic regression to identify factors associated with discordant responses.
RESULTS RESULTS
Among the 123 HIV-1 infected FSW having at least 12 months follow-up on ART, 105 (85.4%) achieved HIV-1 RNA suppression. Among the latter 25 gained less than 100 CD4 + T cells within 12 months follow-up. The IVD rate was 23.8% (95%CI 16.04%-33.11%). After adjustment for age, WHO clinical stage and ART regimen including nucleoside/nucleotide reverse transcriptase inhibitors, only baseline CD4 + T cell count between 200 to 350 cells/µL (adjusted OR: 4.15; 95%CI 1.13-15.22) and 350 to 500 cells/µL (adjusted OR: 17.50; 95%CI 2.68-114.31) remain significantly associated with IVD occurrence.
CONCLUSIONS CONCLUSIONS
Immunovirological discordance response was common in FSW with proportions close to those observed in the general population. A diagnosis and personalized follow-up of patients who do not achieve full immune reconstitution would make it possible to avoid complications in terms of morbidity and mortality.

Identifiants

pubmed: 35114959
doi: 10.1186/s12879-022-07109-8
pii: 10.1186/s12879-022-07109-8
pmc: PMC8812047
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117

Informations de copyright

© 2022. The Author(s).

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Auteurs

Wilfried Wenceslas Bazié (WW)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso. bww_wens@yahoo.fr.

Diane Yirgnur Somé (DY)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Isidore Tiandiogo Traoré (IT)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.
Institut Supérieur des Sciences de la Santé, Université Nazi Boni, Bobo-Dioulasso, Burkina Faso.

Anselme Sanon (A)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Issouf Konaté (I)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.
Institut Supérieur des Sciences de la Santé, Université Nazi Boni, Bobo-Dioulasso, Burkina Faso.

Souleymane Tassembedo (S)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Ajani Ousmane Taofiki (AO)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Dramane Kania (D)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Abdoulaye Ouédraogo (A)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.

Bea Vuylsteke (B)

Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium.

Caroline Gilbert (C)

Axe de Recherche Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.

Nicolas Meda (N)

Centre Muraz, Institut National de Santé Publique, 2054 Avenue Mamadou Konaté01 BP 390, Bobo-Dioulasso, Burkina Faso.
Département de Santé Publique, Unité de Formation et de Recherche en Sciences de la Santé, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso.

Abdoul Salam Ouédraogo (AS)

Institut Supérieur des Sciences de la Santé, Université Nazi Boni, Bobo-Dioulasso, Burkina Faso.

Nicolas Nagot (N)

INSERM, Université des Antilles, Etablissement Français du Sang, Montpellier, France.

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