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. 2023 Apr 1;37(5):709-721.
doi: 10.1097/QAD.0000000000003469. Epub 2022 Dec 22.

Antibody response durability following three-dose coronavirus disease 2019 vaccination in people with HIV receiving suppressive antiretroviral therapy

Affiliations

Antibody response durability following three-dose coronavirus disease 2019 vaccination in people with HIV receiving suppressive antiretroviral therapy

Hope R Lapointe et al. AIDS. .

Abstract

Background: Limited data exist regarding longer term antibody responses following three-dose coronavirus disease 2019 (COVID-19) vaccination, and the impact of a first SARS-CoV-2 infection during this time, in people with HIV (PWH) receiving suppressive antiretroviral therapy (ART). We quantified wild-type-specific, Omicron BA.1-specific and Omicron BA.5-specific responses up to 6 months post-third dose in 64 PWH and 117 controls who remained COVID-19-naive or experienced their first SARS-CoV-2 infection during this time.

Design: Longitudinal observational cohort.

Methods: We quantified wild-type-specific and Omicron-specific anti-Spike receptor-binding domain IgG concentrations, ACE2 displacement activities and live virus neutralization at 1, 3 and 6 months post-third vaccine dose.

Results: Third doses boosted all antibody measures above two-dose levels, but BA.1-specific responses remained significantly lower than wild-type-specific ones, with BA.5-specific responses lower still. Serum IgG concentrations declined at similar rates in COVID-19-naive PWH and controls post-third dose (median wild-type-specific and BA.1-specific half-lives were between 66 and 74 days for both groups). Antibody function also declined significantly yet comparably between groups: 6 months post-third dose, BA.1-specific neutralization was undetectable in more than 80% of COVID-19 naive PWH and more than 90% of controls. Breakthrough SARS-CoV-2 infection boosted antibody concentrations and function significantly above vaccine-induced levels in both PWH and controls, though BA.5-specific neutralization remained significantly poorer than BA.1 even post-breakthrough.

Conclusion: Following three-dose COVID-19 vaccination, antibody response durability in PWH receiving ART is comparable with controls. PWH also mounted strong responses to breakthrough infection. Due to temporal response declines, however, COVID-19-naive individuals, regardless of HIV status, would benefit from a fourth dose within 6 months of their third.

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Conflict of interest statement

There are no conflicts of interest.

Figures

Fig. 1
Fig. 1
Wild-type-specific and Omicron BA.1-specific anti-RBD IgG concentrations following three-dose coronavirus disease 2019 vaccination.
Fig. 2
Fig. 2
Wild-type-specific and Omicron BA.1-specific ACE2 displacement function following three-dose COVID-19 vaccination.
Fig. 3
Fig. 3
Wild-type-specific and Omicron BA.1-specific live virus neutralization activity following three-dose coronavirus disease 2019 vaccination.
Fig. 4
Fig. 4
Wild-type-specific, Omicron BA.1-specific and Omicron BA.5-specific live virus neutralization activity before and after breakthrough infection.

Comment in

References

    1. Barda N, Dagan N, Cohen C, Hernan MA, Lipsitch M, Kohane IS, et al. . Effectiveness of a third dose of the BNT162b2 mRNA COVID-19 vaccine for preventing severe outcomes in Israel: an observational study. Lancet 2021; 398:2093–2100. - PMC - PubMed
    1. Eliakim-Raz N, Leibovici-Weisman Y, Stemmer A, Ness A, Awwad M, Ghantous N, et al. . Antibody titers before and after a third dose of the SARS-CoV-2 BNT162b2 vaccine in adults aged >/=60 years. JAMA 2021; 326:2203–2204. - PMC - PubMed
    1. Moreira ED, Jr, Kitchin N, Xu X, Dychter SS, Lockhart S, Gurtman A, et al. . Safety and efficacy of a third dose of BNT162b2 Covid-19 vaccine. N Engl J Med 2022; 386:1910–1921. - PMC - PubMed
    1. Yoon SK, Hegmann KT, Thiese MS, Burgess JL, Ellingson K, Lutrick K, et al. . HEROES-RECOVER Network Investigators, HEROES-RECOVER Network Investigators. Protection with a third dose of mRNA vaccine against SARS-CoV-2 variants in frontline workers. N Engl J Med 2022; 386:1855–1857. - PMC - PubMed
    1. Tegally H, Moir M, Everatt J, Giovanetti M, Scheepers C, Wilkinson E, et al. . Emergence of SARS-CoV-2 Omicron lineages BA.4 and BA.5 in South Africa. Nat Med 2022; 28:1785–1790. - PMC - PubMed

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