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Immunogenicity of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Ad26.CoV2.S Vaccination in People Living With Human Immunodeficiency Virus (HIV).
Khan, Khadija; Lustig, Gila; Bernstein, Mallory; Archary, Derseree; Cele, Sandile; Karim, Farina; Smith, Muneerah; Ganga, Yashica; Jule, Zesuliwe; Reedoy, Kajal; Miya, Yoliswa; Mthabela, Ntombifuthi; Magula, Nombulelo P; Lessells, Richard; de Oliveira, Tulio; Gosnell, Bernadett I; Abdool Karim, Salim; Garrett, Nigel; Hanekom, Willem; Bekker, Linda-Gail; Gray, Glenda; Blackburn, Jonathan M; Moosa, Mahomed-Yunus S; Sigal, Alex.
  • Khan K; Africa Health Research Institute, Durban, South Africa.
  • Lustig G; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
  • Bernstein M; Centre for the AIDS Programme of Research in South Africa, Durban, South Africa.
  • Archary D; Africa Health Research Institute, Durban, South Africa.
  • Cele S; Centre for the AIDS Programme of Research in South Africa, Durban, South Africa.
  • Karim F; Department of Medical Microbiology, University of KwaZulu-Natal, Durban, South Africa.
  • Smith M; Africa Health Research Institute, Durban, South Africa.
  • Ganga Y; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
  • Jule Z; Africa Health Research Institute, Durban, South Africa.
  • Reedoy K; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
  • Miya Y; Department of Integrative Biomedical Sciences, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Mthabela N; Africa Health Research Institute, Durban, South Africa.
  • Magula NP; Africa Health Research Institute, Durban, South Africa.
  • Lessells R; Africa Health Research Institute, Durban, South Africa.
  • de Oliveira T; Africa Health Research Institute, Durban, South Africa.
  • Gosnell BI; Africa Health Research Institute, Durban, South Africa.
  • Abdool Karim S; Department of Medicine, King Edward VIII Hospital and University of KwaZulu Natal, Durban, South Africa.
  • Garrett N; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
  • Hanekom W; Centre for the AIDS Programme of Research in South Africa, Durban, South Africa.
  • Bekker LG; KwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
  • Gray G; School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.
  • Blackburn JM; Centre for the AIDS Programme of Research in South Africa, Durban, South Africa.
  • Moosa MS; KwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa.
  • Sigal A; Centre for Epidemic Response and Innovation, School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa.
Clin Infect Dis ; 75(1): e857-e864, 2022 Aug 24.
Article in English | MEDLINE | ID: covidwho-2017793
ABSTRACT

BACKGROUND:

People living with HIV (PLWH) have been reported to have a higher risk of more severe COVID-19 disease and death. We assessed the ability of the Ad26.CoV2.S vaccine to elicit neutralizing activity against the Delta variant in PLWH relative to HIV-negative individuals. We also examined effects of HIV status and suppression on Delta neutralization response in SARS-CoV-2-infected unvaccinated participants.

METHODS:

We enrolled participants who were vaccinated through the SISONKE South African clinical trial of the Ad26.CoV2.S vaccine in healthcare workers (HCWs). PLWH in this group had well-controlled HIV infection. We also enrolled unvaccinated participants previously infected with SARS-CoV-2. Neutralization capacity was assessed by a live virus neutralization assay of the Delta variant.

RESULTS:

Most Ad26.CoV2.S vaccinated HCWs were previously infected with SARS-CoV-2. In this group, Delta variant neutralization was 9-fold higher compared with the infected-only group and 26-fold higher relative to the vaccinated-only group. No decrease in Delta variant neutralization was observed in PLWH relative to HIV-negative participants. In contrast, SARS-CoV-2-infected, unvaccinated PLWH showed 7-fold lower neutralization and a higher frequency of nonresponders, with the highest frequency of nonresponders in people with HIV viremia. Vaccinated-only participants showed low neutralization capacity.

CONCLUSIONS:

The neutralization response of the Delta variant following Ad26.CoV2.S vaccination in PLWH with well-controlled HIV was not inferior to HIV-negative participants, irrespective of past SARS-CoV-2 infection. In SARS-CoV-2-infected and nonvaccinated participants, HIV infection reduced the neutralization response to SARS-CoV-2, with the strongest reduction in HIV viremic individuals.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / COVID-19 / Ad26COVS1 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines / Variants Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / COVID-19 / Ad26COVS1 Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines / Variants Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid