Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV

ABSTRACT Few studies have comprehensively compared severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine-induced and hybrid B- and T-cell responses in people with HIV (PWH) to those in comparable controls without HIV. We included 195 PWH and 246 comparable controls from the AGEhIV COV...

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Main Authors: Myrthe L. Verburgh, Lisa van Pul, Marloes Grobben, Anders Boyd, Ferdinand W. N. M. Wit, Ad C. van Nuenen, Karel A. van Dort, Khadija Tejjani, Jacqueline van Rijswijk, Margreet Bakker, Lia van der Hoek, Maarten F. Schim van der Loeff, Marc van der Valk, Marit J. van Gils, Neeltje A. Kootstra, Peter Reiss
Format: Article
Language:English
Published: American Society for Microbiology 2023-06-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.01155-23
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author Myrthe L. Verburgh
Lisa van Pul
Marloes Grobben
Anders Boyd
Ferdinand W. N. M. Wit
Ad C. van Nuenen
Karel A. van Dort
Khadija Tejjani
Jacqueline van Rijswijk
Margreet Bakker
Lia van der Hoek
Maarten F. Schim van der Loeff
Marc van der Valk
Marit J. van Gils
Neeltje A. Kootstra
Peter Reiss
author_facet Myrthe L. Verburgh
Lisa van Pul
Marloes Grobben
Anders Boyd
Ferdinand W. N. M. Wit
Ad C. van Nuenen
Karel A. van Dort
Khadija Tejjani
Jacqueline van Rijswijk
Margreet Bakker
Lia van der Hoek
Maarten F. Schim van der Loeff
Marc van der Valk
Marit J. van Gils
Neeltje A. Kootstra
Peter Reiss
author_sort Myrthe L. Verburgh
collection DOAJ
description ABSTRACT Few studies have comprehensively compared severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine-induced and hybrid B- and T-cell responses in people with HIV (PWH) to those in comparable controls without HIV. We included 195 PWH and 246 comparable controls from the AGEhIV COVID-19 substudy. A positive nucleocapsid antibody (INgezim IgA/IgM/IgG) or self-reported PCR test defined prior SARS-CoV-2 infection. SARS-CoV-2 anti-spike (anti-S) IgG titers and anti-S IgG production by memory B cells were assessed. Neutralizing antibody titers were determined in a subset of participants. T-cell responses were assessed by gamma interferon (IFN-γ) release and activation-induced marker assay. We estimated mean differences in postvaccination immune responses (β) between levels of determinants. Anti-S IgG titers and anti-S IgG production by memory B cells were not different between PWH and controls. Prior SARS-CoV-2 infection (β = 0.77), receiving mRNA vaccine (β = 0.56), female sex (β = 0.24), fewer days between last vaccination and sampling (β = 0.07), and a CD4/CD8 ratio of <1.0 (β = −0.39) were independently associated with anti-S IgG titers, but HIV status was not. Neutralization titers against the ancestral and Delta and Omicron SARS-CoV-2 variants were not different between PWH and controls. IFN-γ release was higher in PWH. Prior SARS-CoV-2 infection (β = 2.39), HIV-positive status (β = 1.61), and fewer days between last vaccination and sampling (β = 0.23) were independently associated with higher IFN-γ release. The percentages of SARS-CoV-2-reactive CD4+ and CD8+ T cells, however, were not different between PWH and controls. Individuals with well-controlled HIV generally mount robust vaccine-induced as well as hybrid B- and T-cell immunity across SARS-CoV-2 vaccine platforms similar to controls. Determinants of a reduced vaccine response were likewise largely similar in both groups and included a lower CD4/CD8 ratio. IMPORTANCE Some studies have suggested that people with HIV may respond less well to vaccines against SARS-CoV-2. We comprehensively compared B- and T-cell responses to different COVID-19 vaccines in middle-aged persons with well-treated HIV and individuals of the same age without HIV, who were also highly comparable in terms of demographics and lifestyle, including those with prior SARS-CoV-2 infection. Individuals with HIV generally mounted equally robust immunity to the different vaccines. Even stronger immunity was observed in both groups after prior SARS-CoV-2 infection. These findings are reassuring with respect to the efficacy of SARS-Cov-2 vaccines for the sizable and increasing global population of people with HIV with access and a good response to HIV treatment.
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spelling doaj.art-e41f2eae979f452e9fbb2e5eaf37db882023-06-15T13:18:33ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972023-06-0111310.1128/spectrum.01155-23Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIVMyrthe L. Verburgh0Lisa van Pul1Marloes Grobben2Anders Boyd3Ferdinand W. N. M. Wit4Ad C. van Nuenen5Karel A. van Dort6Khadija Tejjani7Jacqueline van Rijswijk8Margreet Bakker9Lia van der Hoek10Maarten F. Schim van der Loeff11Marc van der Valk12Marit J. van Gils13Neeltje A. Kootstra14Peter Reiss15Amsterdam UMC, University of Amsterdam, Infectious Diseases, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsHIV Monitoring Foundation, Amsterdam, The NetherlandsAmsterdam UMC, University of Amsterdam, Infectious Diseases, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam UMC, University of Amsterdam, Infectious Diseases, Amsterdam, The NetherlandsAmsterdam UMC, University of Amsterdam, Infectious Diseases, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam Institute for Infection and Immunity, Amsterdam, The NetherlandsAmsterdam UMC, University of Amsterdam, Infectious Diseases, Amsterdam, The NetherlandsABSTRACT Few studies have comprehensively compared severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine-induced and hybrid B- and T-cell responses in people with HIV (PWH) to those in comparable controls without HIV. We included 195 PWH and 246 comparable controls from the AGEhIV COVID-19 substudy. A positive nucleocapsid antibody (INgezim IgA/IgM/IgG) or self-reported PCR test defined prior SARS-CoV-2 infection. SARS-CoV-2 anti-spike (anti-S) IgG titers and anti-S IgG production by memory B cells were assessed. Neutralizing antibody titers were determined in a subset of participants. T-cell responses were assessed by gamma interferon (IFN-γ) release and activation-induced marker assay. We estimated mean differences in postvaccination immune responses (β) between levels of determinants. Anti-S IgG titers and anti-S IgG production by memory B cells were not different between PWH and controls. Prior SARS-CoV-2 infection (β = 0.77), receiving mRNA vaccine (β = 0.56), female sex (β = 0.24), fewer days between last vaccination and sampling (β = 0.07), and a CD4/CD8 ratio of <1.0 (β = −0.39) were independently associated with anti-S IgG titers, but HIV status was not. Neutralization titers against the ancestral and Delta and Omicron SARS-CoV-2 variants were not different between PWH and controls. IFN-γ release was higher in PWH. Prior SARS-CoV-2 infection (β = 2.39), HIV-positive status (β = 1.61), and fewer days between last vaccination and sampling (β = 0.23) were independently associated with higher IFN-γ release. The percentages of SARS-CoV-2-reactive CD4+ and CD8+ T cells, however, were not different between PWH and controls. Individuals with well-controlled HIV generally mount robust vaccine-induced as well as hybrid B- and T-cell immunity across SARS-CoV-2 vaccine platforms similar to controls. Determinants of a reduced vaccine response were likewise largely similar in both groups and included a lower CD4/CD8 ratio. IMPORTANCE Some studies have suggested that people with HIV may respond less well to vaccines against SARS-CoV-2. We comprehensively compared B- and T-cell responses to different COVID-19 vaccines in middle-aged persons with well-treated HIV and individuals of the same age without HIV, who were also highly comparable in terms of demographics and lifestyle, including those with prior SARS-CoV-2 infection. Individuals with HIV generally mounted equally robust immunity to the different vaccines. Even stronger immunity was observed in both groups after prior SARS-CoV-2 infection. These findings are reassuring with respect to the efficacy of SARS-Cov-2 vaccines for the sizable and increasing global population of people with HIV with access and a good response to HIV treatment.https://journals.asm.org/doi/10.1128/spectrum.01155-23HIVSARS-CoV-2 vaccineshumoral immune responsescellular immune responses
spellingShingle Myrthe L. Verburgh
Lisa van Pul
Marloes Grobben
Anders Boyd
Ferdinand W. N. M. Wit
Ad C. van Nuenen
Karel A. van Dort
Khadija Tejjani
Jacqueline van Rijswijk
Margreet Bakker
Lia van der Hoek
Maarten F. Schim van der Loeff
Marc van der Valk
Marit J. van Gils
Neeltje A. Kootstra
Peter Reiss
Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
Microbiology Spectrum
HIV
SARS-CoV-2 vaccines
humoral immune responses
cellular immune responses
title Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
title_full Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
title_fullStr Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
title_full_unstemmed Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
title_short Robust Vaccine-Induced as Well as Hybrid B- and T-Cell Immunity across SARS-CoV-2 Vaccine Platforms in People with HIV
title_sort robust vaccine induced as well as hybrid b and t cell immunity across sars cov 2 vaccine platforms in people with hiv
topic HIV
SARS-CoV-2 vaccines
humoral immune responses
cellular immune responses
url https://journals.asm.org/doi/10.1128/spectrum.01155-23
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