<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hicks J</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>National Institute of Allergy and Infectious Diseases</funding><funding>CCR NIH HHS</funding><funding>NIBIB NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><pagination>906-913</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7962425</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(5)</volume><pubmed_abstract>In order to properly understand the spread of SARS-CoV-2 infection and development of humoral immunity, researchers have evaluated the presence of serum antibodies of people worldwide experiencing the pandemic. These studies rely on the use of recombinant proteins from the viral genome in order to identify serum antibodies that recognize SARS-CoV-2 epitopes. Here, we discuss the cross-reactivity potential of SARS-CoV-2 antibodies with the full spike proteins of four other betacoronaviruses that cause disease in humans, MERS-CoV, SARS-CoV, HCoV-OC43, and HCoV-HKU1. Using enzyme-linked immunosorbent assays (ELISAs), we detected the potential cross-reactivity of antibodies against SARS-CoV-2 towards the four other coronaviruses, with the strongest cross-recognition between SARS-CoV-2 and SARS /MERS-CoV antibodies, as expected based on sequence homology of their respective spike proteins. Further analysis of cross-reactivity could provide informative data that could lead to intelligently designed pan-coronavirus therapeutics or vaccines.</pubmed_abstract><journal>Journal of clinical immunology</journal><pubmed_title>Serologic Cross-Reactivity of SARS-CoV-2 with Endemic and Seasonal Betacoronaviruses.</pubmed_title><pmcid>PMC7962425</pmcid><funding_grant_id>HHSN261200800001E</funding_grant_id><funding_grant_id>HHSN261200800001C</funding_grant_id><funding_grant_id>Intramural Research Program</funding_grant_id><pubmed_authors>Corbett KS</pubmed_authors><pubmed_authors>Sadtler K</pubmed_authors><pubmed_authors>Klumpp-Thomas C</pubmed_authors><pubmed_authors>Hicks J</pubmed_authors><pubmed_authors>Kalish H</pubmed_authors><pubmed_authors>Graham BS</pubmed_authors><pubmed_authors>Drew M</pubmed_authors><pubmed_authors>Shunmugavel A</pubmed_authors><pubmed_authors>Hall MD</pubmed_authors><pubmed_authors>Mehalko J</pubmed_authors><pubmed_authors>Snead KR</pubmed_authors><pubmed_authors>Memoli MJ</pubmed_authors><pubmed_authors>Denson JP</pubmed_authors><pubmed_authors>Esposito D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serologic Cross-Reactivity of SARS-CoV-2 with Endemic and Seasonal Betacoronaviruses.</name><description>In order to properly understand the spread of SARS-CoV-2 infection and development of humoral immunity, researchers have evaluated the presence of serum antibodies of people worldwide experiencing the pandemic. These studies rely on the use of recombinant proteins from the viral genome in order to identify serum antibodies that recognize SARS-CoV-2 epitopes. Here, we discuss the cross-reactivity potential of SARS-CoV-2 antibodies with the full spike proteins of four other betacoronaviruses that cause disease in humans, MERS-CoV, SARS-CoV, HCoV-OC43, and HCoV-HKU1. Using enzyme-linked immunosorbent assays (ELISAs), we detected the potential cross-reactivity of antibodies against SARS-CoV-2 towards the four other coronaviruses, with the strongest cross-recognition between SARS-CoV-2 and SARS /MERS-CoV antibodies, as expected based on sequence homology of their respective spike proteins. Further analysis of cross-reactivity could provide informative data that could lead to intelligently designed pan-coronavirus therapeutics or vaccines.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-18T16:39:41.312Z</modification><creation>2025-04-07T04:00:44.383Z</creation></dates><accession>S-EPMC7962425</accession><cross_references><pubmed>33725211</pubmed><doi>10.1007/s10875-021-00997-6</doi></cross_references></HashMap>