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Immunogenicity of the Ad26.CoV2.S vaccine in people living with HIV
Khadija Khan; Gila Lustig; Mallory Bernstein; Derseree Archary; Sandile Cele; Farina Karim; Muneerah Smith; Yashica Ganga; Zesuliwe Jule; Kajal Reedoy; Yoliswa Miya; Ntombifuthi Mthabela; - COMMIT-KZN Team; Richard Lessells; Tulio de Oliveira; Bernadett Gosnell; Salim Abdool Karim; Nigel Garrett; Willem Hanekom; Linda Gail Bekker; Glenda Gray; Jonathan M Blackburn; Mahomed-Yunus S Moosa; Alex Sigal.
Afiliação
  • Khadija Khan; Africa Health Research Institute; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal
  • Gila Lustig; Centre for the AIDS Programme of Research in South Africa
  • Mallory Bernstein; Africa Health Research Institute
  • Derseree Archary; Centre for the AIDS Programme of Research in South Africa; Department of Medical Microbiology, University of KwaZulu-Natal
  • Sandile Cele; Africa Health Research Institute; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal
  • Farina Karim; Africa Health Research Institute; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal
  • Muneerah Smith; Department of Integrative Biomedical Sciences
  • Yashica Ganga; Africa Health Research Institute
  • Zesuliwe Jule; Africa Health Research Institute
  • Kajal Reedoy; Africa Health Research Institute
  • Yoliswa Miya; Africa Health Research Institute
  • Ntombifuthi Mthabela; Africa Health Research Institute
  • - COMMIT-KZN Team;
  • Richard Lessells; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa; Centre for the AIDS Programme of Research in South Africa
  • Tulio de Oliveira; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa; Centre for the AIDS Programme of Research in South Africa
  • Bernadett Gosnell; Department of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal
  • Salim Abdool Karim; Centre for the AIDS Programme of Research in South Africa
  • Nigel Garrett; Centre for the AIDS Programme of Research in South Africa; Discipline of Public Health Medicine, School of Nursing and Public Health, University of KwaZulu-Nata
  • Willem Hanekom; Africa Health Research Institute; Division of Infection and Immunity, University College London
  • Linda Gail Bekker; Institute of Infectious Disease and Molecular Medicine; Desmond Tutu HIV Centre
  • Glenda Gray; South African Medical Research Council
  • Jonathan M Blackburn; Department of Integrative Biomedical Sciences; Institute of Infectious Disease and Molecular Medicine; Sengenics Corporation, Kuala Lumpur, Malaysia
  • Mahomed-Yunus S Moosa; Department of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal
  • Alex Sigal; Africa Health Research Institute
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21264519
ABSTRACT
BackgroundPeople living with HIV (PLWH) have been reported to have an increased risk of more severe COVID-19 disease outcome and an increased risk of death relative to HIV-uninfected individuals. Here we assessed the ability of the Johnson and Johnson Ad26.CoV2.S vaccine to elicit neutralizing antibodies to the Delta variant in PLWH relative to HIV-uninfected individuals. We also compared the neutralization after vaccination to neutralization elicited by SARS-CoV-2 infection only in HIV-uninfected, suppressed HIV PLWH, and PLWH with detectable HIV viremia. MethodsWe enrolled 26 PLWH and 73 HIV-uninfected participants from the SISONKE phase 3b open label South African clinical trial of the Ad26.CoV2.S vaccine in health care workers (HCW). Enrollment was a median 56 days (range 19-98 days) post-vaccination and PLWH in this group had well controlled HIV infection. We also enrolled unvaccinated participants previously infected with SARS-CoV-2. This group consisted of 34 PLWH and 28 HIV-uninfected individuals. 10 of the 34 (29%) SARS-CoV-2 infected only PLWH had detectable HIV viremia. We used records of a positive SARS-CoV-2 qPCR result, or when a positive result was absent, testing for SARS-CoV-2 nucleocapsid antibodies, to determine which vaccinated participants were SARS-CoV-2 infected prior to vaccination. Neutralization capacity was assessed using participant plasma in a live virus neutralization assay of the Delta SARS-CoV-2 variant currently dominating infections in South Africa. This study was approved by the Biomedical Research Ethics Committee at the University of KwaZulu-Natal (reference BREC/00001275/2020). FindingsThe majority (68%) of Ad26.CoV2.S vaccinated HCW were found to be previously infected with SARS-CoV-2. In this group, Delta variant neutralization was 9-fold higher compared to the infected only group (GMT=306 versus 36, p<0.0001) and 26-fold higher relative to the vaccinated only group (GMT=12, p<0.0001). No significant difference in Delta variant neutralization capacity was observed in vaccinated and previously SARS-CoV-2 infected PLWH relative to vaccinated and previously SARS-CoV-2 infected, HIV-uninfected participants (GMT=307 for HIV-uninfected, 300 for PLWH, p=0.95). SARS-CoV-2 infected, unvaccinated PLWH showed 7-fold reduced neutralization of the Delta variant relative to HIV-uninfected participants (GMT=105 for HIV-uninfected, 15 for PLWH, p=0.001). There was a higher frequency of non-responders in PLWH relative to HIV-uninfected participants in the SARS-CoV-2 infected unvaccinated group (27% versus 0%, p=0.0029) and 60% of HIV viremic versus 13% of HIV suppressed PLWH were non-responders (p=0.0088). In contrast, the frequency of non-responders was low in the vaccinated/infected group, and similar between HIV-uninfected and PLWH. Vaccinated only participants showed a low neutralization of the Delta variant, with a stronger response in PLWH (GMT=6 for HIV-uninfected, 73 for PLWH, p=0.02). InterpretationThe neutralization response of the Delta variant following Ad26.CoV2.S vaccination in PLWH with well controlled HIV was not inferior to HIV-uninfected study participants. In SARS-CoV-2 infected and non-vaccinated participants, the presence of HIV infection reduced the neutralization response to SARS-CoV-2 infection, and this effect was strongest in PLWH with detectable HIV viremia FundingSouth African Medical Research Council, The Bill & Melinda Gates Foundation.
Licença
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Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint