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Article ; Online: Neutralizing antibody response to SARS-CoV-2 bivalent mRNA vaccine in SIV-infected rhesus macaques: Enhanced immunity to XBB subvariants by two-dose vaccination.

Faraone, Julia N / Wang, Xiaolwei / Qu, Panke / Zheng, Yi-Min / Vincent, Eunice / Xu, Huanbin / Liu, Shan-Lu

Journal of medical virology

2024  Volume 96, Issue 3, Page(s) e29520

Abstract: The evolution of SARS-CoV-2 paired with immune imprinting by prototype messenger RNA (mRNA) vaccine has challenged the current vaccination efficacy against newly emerged Omicron subvariants. In our study, we investigated a cohort of macaques infected by ... ...

Abstract The evolution of SARS-CoV-2 paired with immune imprinting by prototype messenger RNA (mRNA) vaccine has challenged the current vaccination efficacy against newly emerged Omicron subvariants. In our study, we investigated a cohort of macaques infected by SIV and vaccinated with two doses of bivalent Pfizer mRNA vaccine containing wildtype and BA.5 spikes. Using a pseudotyped lentivirus neutralization assay, we determined neutralizing antibody (nAb) titers against new XBB variants, i.e., XBB.1.5, XBB.1.16, and XBB.2.3, alongside D614G and BA.4/5. We found that compared to humans vaccinated with three doses of monovalent mRNA vaccine plus a bivalent booster, the monkeys vaccinated with two doses of bivalent mRNA vaccines exhibited relatively increased titers against XBB subvariants. Of note, SIV-positive dam macaques had reduced nAb titers relative to SIV-negative dams. Additionally, SIV positive dams that received antiretroviral therapy had lower nAb titers than untreated dams. Our study underscores the importance of reformulating the COVID-19 vaccine to better protect against newly emerged XBB subvariants as well as the need for further investigation of vaccine efficacy in individuals living with HIV-1.
MeSH term(s) Humans ; Animals ; Macaca mulatta ; Vaccines, Combined ; mRNA Vaccines ; SARS-CoV-2/genetics ; COVID-19 Vaccines ; COVID-19/prevention & control ; Vaccination ; Antibodies, Neutralizing ; RNA, Messenger ; Antibodies, Viral
Chemical Substances Vaccines, Combined ; mRNA Vaccines ; COVID-19 Vaccines ; Antibodies, Neutralizing ; RNA, Messenger ; Antibodies, Viral
Language English
Publishing date 2024-03-26
Publishing country United States
Document type Journal Article
ZDB-ID 752392-0
ISSN 1096-9071 ; 0146-6615
ISSN (online) 1096-9071
ISSN 0146-6615
DOI 10.1002/jmv.29520
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