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Pre-existing IgG antibodies to HCoVs NL63 and OC43 spike increased during the pandemic and after COVID-19 vaccination

dc.contributor.authorHasan, Zahra
dc.contributor.authorMasood, Kiran Iqbal
dc.contributor.authorVeldhoen, Marc
dc.contributor.authorQaiser, Shama
dc.contributor.authorAlenquer, Marta
dc.contributor.authorAkhtar, Mishgan
dc.contributor.authorBalouch, Sadaf
dc.contributor.authorIqbal, Junaid
dc.contributor.authorWassan, Yaqub
dc.contributor.authorHussain, Shahneel
dc.contributor.authorFeroz, Khalid
dc.contributor.authorMuhammad, Sajid
dc.contributor.authorHabib, Atif
dc.contributor.authorKanji, Akbar
dc.contributor.authorKhan, Erum
dc.contributor.authorMian, Afsar Ali
dc.contributor.authorHussain, Rabia
dc.contributor.authorAmorim, Maria Joao
dc.contributor.authorBhutta, Zulfiqar A.
dc.date.accessioned2025-02-04T12:00:46Z
dc.date.available2025-02-04T12:00:46Z
dc.date.issued2025-02-15
dc.description.abstractPreexisting immunity may be associated with increased protection against non-related pathogens such as, SARS-CoV-2. There is little information regarding endemic human coronaviruses (HCOVs) from Pakistan, which experienced a relatively low COVID-19 morbidity and mortality. We investigated antibodies to SARS-CoV-2 and HCoVs NL63 and OC43, comparing sera from prepandemic controls (PPC) period with responses in healthy controls from the pandemic (HC 2021). Further, we investigated the effect of inactivated and mRNA COVID-19 vaccinations on antibody responses to the pandemic and endemic coronaviruses. We measured IgG antibodies to Spike of SARS-CoV-2, HCoV-NL63 and HCoV-OC43 by ELISA. Serum neutralizing capacity was determined using a SARS-CoV-2 psuedotyped virus assay. Vaccinees were sampled prior to vaccination as well after 6, 12 and 24 weeks after COVID-19 inactivated (Sinovac), or mRNA (BNT162b2) vaccine administration. PPC sera showed seropositivity of 15 % to SARS-CoV-2, whilst it was 45 % in the HC 2021 group. Five percent of sera showed virus neutralizing activity in PPC whilst it was 50 % in HC 2021. IgG antibodies to Spike of NL63 and OC43 were also present in PPC; anti-NL63 was 2.9-fold, and anti-OC43 was 10.1-fold higher than to anti-SARS-CoV-2 levels. IgG antibodies to Spike SARS-CoV-2 were positively correlated with HCoV-NL63 in HC 2021, indicating recognition of shared conserved epitopes. IgG antibody levels increased during the pandemic; 2.7-fold to HCoV-NL63 and 1.9-fold to HCoV-OC43. SinoVac and BNT162b2 vaccine induced an increase in IgG antibodies to Spike SARS-CoV-2 as well as HCoV-NL63 and HCoV-OC43. Our data show that antibodies to spike protein of endemic coronaviruses were present in the prepandemic population. Antibodies to SARS-CoV-2, NL63 and OC43 were all raised during the pandemic and further enhanced after COVID-19 vaccinations. The increase in antibodies to spike of coronaviruses would contribute to protection against SARS-CoV-2.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.heliyon.2025.e42171pt_PT
dc.identifier.eid85215988156
dc.identifier.issn2405-8440
dc.identifier.pmid39916832
dc.identifier.pmidPMC11795784
dc.identifier.urihttp://hdl.handle.net/10400.14/48039
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.titlePre-existing IgG antibodies to HCoVs NL63 and OC43 spike increased during the pandemic and after COVID-19 vaccinationpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue3pt_PT
oaire.citation.titleHeliyonpt_PT
oaire.citation.volume11pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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