Neutralizing antibody responses assessment after vaccination in People Living with HIV in the Republic of the Congo

Author:

Batchi-Bouyou Armel Landry1,Djontu Jean Claude2,Ingoba Line Lobaloba2,Mougany Jiré Séphora2,Mouzinga Freisnel Hermeland2,Ntabi Jacques Dollon Mbama2,Kouikani Franck Yannis3,Ndala Arcel Christ Massamba4,Diafouka-kietela Steve2,Ampa Raoul5,Ntoumi Francine2

Affiliation:

1. Harvard Medical School

2. Fondation Congolaise pour la Recherche Médicale (FCRM)

3. Department of Health and Social Care, Ministry of Higher Education, Scientific Research and Technological Innovation, Congo

4. Ambulatory Treatment Center, National HIV Program, Ministry of Health and Population

5. University Marien Ngouabi

Abstract

Abstract Objective HIV has been reported to interfere with protective vaccination against multiple pathogens, usually through the decreased effectiveness of the antibody responses. We aimed to assess neutralizing antibody responses induced by COVID-19 vaccination in PLWH in Brazzaville, Republique of Congo Method The study was conducted at the Ambulatory Treatment Center of the National HIV Program, in charge of over 6000 PLWH, and the health center of FCRM in Brazzaville, Republic of the Congo.Participants were divided into two groups: PLWH with well-controlled HIV infection (CD4 counts no older than one week ≥ 800 / mm3, undetectable viral load of a period no older than one week and regularly taking Highly Active Antiretroviral Therapy for at least 6 months) and the non-PLWH (healthy HIV-negative volunteers). These groups were subdivided by vaccination status: fully Vaccinated with adenovirus-based vaccines (Janssen/Ad26.COV2.S and Sputnik/Gam-COVID-Vac) or inactivated virus vaccine (Sinopharm/BBIP-CorV) and a control group of unvaccinated healthy individuals. All participants were RT-PCR negative at inclusion and/or with no documented history of SARS-CoV-2 infection. ELISA method was used for detecting IgG and neutralizing Antibodies against SARS-CoV-2 antigens using a commercial neutralizing assay. All participants were RT-PCR negative at inclusion and/or with no documented history of SARS-CoV-2 infection. Results We collected oropharyngeal and blood samples from 1016 participants including 684 PLWH and 332 non-PLWH. Both PLWH and non-PLWH elicited high levels of antibody responses after complete vaccination with inactivated virus vaccine (Sinopharm/BBIP-CorV) and adenovirus-based vaccines (Janssen/Ad26.COV2.S and Sputnik/Gam-COVID-Vac). Overall, no difference was observed in neutralization capacity between non-PLWH and PLWH with well-controlled HIV infection. Conclusion The results from this study underline the importance of implementing integrated health systems that provide PLWH the opportunity to benefit HIV prevention and care, at the same time with monitoring their vaccine-induced antibody kinetics for appropriate booster schedules.

Publisher

Research Square Platform LLC

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