{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T11:03:29Z","timestamp":1785409409103,"version":"3.56.0"},"reference-count":46,"publisher":"American Society for Microbiology","issue":"1","license":[{"start":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T00:00:00Z","timestamp":1767657600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T00:00:00Z","timestamp":1767657600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/100011094","name":"Public Health Agency of Canada","doi-asserted-by":"publisher","award":["2021-HQ-000066"],"award-info":[{"award-number":["2021-HQ-000066"]}],"id":[{"id":"10.13039\/100011094","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2026,1,6]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Antibody surveillance provided valuable public health insights during the Coronavirus Disease 2019 (COVID-19) pandemic. Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, vaccination, and cross-reactive responses from endemic coronaviruses (human coronaviruses [HCoVs]) can influence SARS-CoV-2 antibody responses, impacting reliability and interpretation of serological findings. Here, we investigated population-level SARS-CoV-2 and HCoV IgA and IgG responses following SARS-CoV-2 infection among unvaccinated and vaccinated pregnant individuals over 3 months. Using residual sera from routine antenatal screening of pregnant individuals in British Columbia between March 2020 to May 2022, we designed a retrospective repeated cross-sectional cohort of infected individuals either unvaccinated (UV + COV,\n                      <jats:italic toggle=\"yes\">N<\/jats:italic>\n                      = 171) or two- to three-dose vaccinated (V + COV,\n                      <jats:italic toggle=\"yes\">N<\/jats:italic>\n                      = 137). A total of 30 pre-pandemic sera served as negative controls. Sera were collected within 3 months of respiratory PCR-positivity in half-month intervals and tested for IgA and IgG against Spike (S) of alpha-HCoV (HCoV-229E, HCoV-NL63) and beta-HCoV (HCoV-HKU1, HCoV-OC43) and S, receptor binding domain, and nucleocapsid (N) of SARS-CoV-2 using a multiplex immunoassay. Following SARS-CoV-2 infection, V + COV had lower anti-N IgG levels (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = 0.004) and seropositivity rates than UV + COV. One month post-infection, V + COV (38%) had lower anti-N IgA seropositivity than UV + COV (73%). Both groups had significantly higher anti-S IgA and IgG levels against beta-HCoV vs controls, with signals correlating positively with SARS-CoV-2 anti-S levels for each isotype. These results suggest that neither IgA nor IgG can reliably identify recent infections in vaccinated populations, emphasizing the importance of considering complex interplay of antibody responses when interpreting serological data and recognizing the potential and limitations of serological testing for diagnostics and surveillance.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>This study provides key insights into how Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) vaccination and infection shape the magnitude and longevity of IgA and IgG antibody responses following infection in pregnant individuals. It also highlights the interplay of serological responses to related viruses, such as the human coronaviruses. By leveraging population-level antenatal sera, our findings highlight important considerations for the design and interpretation of future seroprevalence studies, antibody-based surveillance, and diagnostic strategies. As SARS-CoV-2 transitions into endemic circulation, understanding the complexity of SARS-CoV-2 antibody responses provides additional insights into the strengths and limitations of serological data interpretation in a real-world setting.<\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.02167-25","type":"journal-article","created":{"date-parts":[[2025,12,5]],"date-time":"2025-12-05T11:03:11Z","timestamp":1764932591000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Serological evaluation of coronavirus IgA and IgG antibodies in a repeated cross-sectional cohort of unvaccinated and vaccinated pregnant individuals over three months following SARS-CoV-2 infection"],"prefix":"10.1128","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7592-8434","authenticated-orcid":false,"given":"Guadalein","family":"Tanunliong","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03rmrcq20","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Pathology and Laboratory Medicine, University of British Columbia","place":["Vancouver, Canada"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana Citlali","family":"M\u00e1rquez","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04gvvdt54","id-type":"ROR","asserted-by":"publisher"}],"name":"Public Health Laboratory, British Columbia Centre for Disease Control","place":["Vancouver, Canada"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hind","family":"Sbihi","sequence":"additional","affiliation":[{"name":"Data and Analytics, British Columbia Centre for Disease Control","place":["Vancouver, 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Fang","family":"Li","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03rmrcq20","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Pathology and Laboratory Medicine, University of British Columbia","place":["Vancouver, Canada"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Danielle","family":"Luk","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04gvvdt54","id-type":"ROR","asserted-by":"publisher"}],"name":"Public Health Laboratory, British Columbia Centre for Disease Control","place":["Vancouver, Canada"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lucia","family":"Forward","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/0455vfz21","id-type":"ROR","asserted-by":"publisher"}],"name":"Women\u2019s Health Research Institute","place":["Vancouver, 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