A New SARS-CoV-2 Dual-Purpose Serology Test: Highly Accurate Infection Tracing and Neutralizing Antibody Response Detection
Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-...
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Published in | Journal of clinical microbiology Vol. 59; no. 4 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
19.03.2021
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Subjects | |
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Abstract | Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies.
Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. The cPass surrogate virus neutralization test (sVNT), compared directly with eight SARS-CoV-2 IgG serology and two live-cell neutralization tests, gives similar or improved accuracy for qualitative delineation between positive and negative individuals in a fast, scalable, and high-throughput assay. The combined data support the cPass sVNT as a tool for highly accurate SARS-CoV-2 immunity surveillance of infected/recovered and/or vaccinated individuals as well as drug and convalescent-phase donor screening. The data also preview a novel application for the cPass sVNT in calibrating the stringency of live-cell neutralization tests and its use in longitudinal testing of recovered and/or vaccinated patients. |
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AbstractList | Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. The cPass surrogate virus neutralization test (sVNT), compared directly with eight SARS-CoV-2 IgG serology and two live-cell neutralization tests, gives similar or improved accuracy for qualitative delineation between positive and negative individuals in a fast, scalable, and high-throughput assay. The combined data support the cPass sVNT as a tool for highly accurate SARS-CoV-2 immunity surveillance of infected/recovered and/or vaccinated individuals as well as drug and convalescent-phase donor screening. The data also preview a novel application for the cPass sVNT in calibrating the stringency of live-cell neutralization tests and its use in longitudinal testing of recovered and/or vaccinated patients.Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. The cPass surrogate virus neutralization test (sVNT), compared directly with eight SARS-CoV-2 IgG serology and two live-cell neutralization tests, gives similar or improved accuracy for qualitative delineation between positive and negative individuals in a fast, scalable, and high-throughput assay. The combined data support the cPass sVNT as a tool for highly accurate SARS-CoV-2 immunity surveillance of infected/recovered and/or vaccinated individuals as well as drug and convalescent-phase donor screening. The data also preview a novel application for the cPass sVNT in calibrating the stringency of live-cell neutralization tests and its use in longitudinal testing of recovered and/or vaccinated patients. Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. The cPass surrogate virus neutralization test (sVNT), compared directly with eight SARS-CoV-2 IgG serology and two live-cell neutralization tests, gives similar or improved accuracy for qualitative delineation between positive and negative individuals in a fast, scalable, and high-throughput assay. The combined data support the cPass sVNT as a tool for highly accurate SARS-CoV-2 immunity surveillance of infected/recovered and/or vaccinated individuals as well as drug and convalescent-phase donor screening. The data also preview a novel application for the cPass sVNT in calibrating the stringency of live-cell neutralization tests and its use in longitudinal testing of recovered and/or vaccinated patients. Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. Many severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology tests have proven to be less accurate than expected and do not assess antibody function as neutralizing, correlating with protection from reinfection. A new assay technology measuring the interaction of the purified SARS-CoV-2 spike protein receptor binding domain (RBD) with the extracellular domain of the human angiotensin-converting enzyme 2 (hACE2) receptor detects these important antibodies. The cPass surrogate virus neutralization test (sVNT), compared directly with eight SARS-CoV-2 IgG serology and two live-cell neutralization tests, gives similar or improved accuracy for qualitative delineation between positive and negative individuals in a fast, scalable, and high-throughput assay. The combined data support the cPass sVNT as a tool for highly accurate SARS-CoV-2 immunity surveillance of infected/recovered and/or vaccinated individuals as well as drug and convalescent-phase donor screening. The data also preview a novel application for the cPass sVNT in calibrating the stringency of live-cell neutralization tests and its use in longitudinal testing of recovered and/or vaccinated patients. |
Author | Annen, Kyle Taylor, Sean C. Kanji, Jamil N. Huey, Leah Knight, Vijaya McCarthy, Mary K. Morrison, Thomas E. Charlton, Carmen L. Bailey, Ashley DomBourian, Melkon G. Hurst, Beth |
Author_xml | – sequence: 1 givenname: Sean C. orcidid: 0000-0003-3411-0673 surname: Taylor fullname: Taylor, Sean C. organization: GenScript USA Inc., Piscataway, New Jersey, USA – sequence: 2 givenname: Beth surname: Hurst fullname: Hurst, Beth organization: Cayman Chemical, Ann Arbor, Michigan, USA – sequence: 3 givenname: Carmen L. orcidid: 0000-0002-9129-5136 surname: Charlton fullname: Charlton, Carmen L. organization: Public Health Laboratory, Alberta Precision Laboratories (ProvLab), University of Alberta Hospital, Edmonton, AB, Canada, Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada, Li Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada – sequence: 4 givenname: Ashley surname: Bailey fullname: Bailey, Ashley organization: Public Health Laboratory, Alberta Precision Laboratories (ProvLab), University of Alberta Hospital, Edmonton, AB, Canada – sequence: 5 givenname: Jamil N. surname: Kanji fullname: Kanji, Jamil N. organization: Public Health Laboratory, Alberta Precision Laboratories (ProvLab), University of Alberta Hospital, Edmonton, AB, Canada, Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, AB, Canada – sequence: 6 givenname: Mary K. surname: McCarthy fullname: McCarthy, Mary K. organization: Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado, USA – sequence: 7 givenname: Thomas E. surname: Morrison fullname: Morrison, Thomas E. organization: Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado, USA – sequence: 8 givenname: Leah surname: Huey fullname: Huey, Leah organization: Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA, Department of Pediatrics, Children’s Hospital Colorado Anschutz Medical Campus, Aurora, Colorado, USA – sequence: 9 givenname: Kyle surname: Annen fullname: Annen, Kyle organization: Department of Pathology and Laboratory Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA, Department of Pathology and Laboratory Medicine, Children’s Hospital Colorado Anschutz Medical Campus, Aurora, Colorado, USA – sequence: 10 givenname: Melkon G. surname: DomBourian fullname: DomBourian, Melkon G. organization: Department of Pathology and Laboratory Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA, Department of Pathology and Laboratory Medicine, Children’s Hospital Colorado Anschutz Medical Campus, Aurora, Colorado, USA – sequence: 11 givenname: Vijaya surname: Knight fullname: Knight, Vijaya organization: Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA, Department of Pediatrics, Children’s Hospital Colorado Anschutz Medical Campus, Aurora, Colorado, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33500361$$D View this record in MEDLINE/PubMed |
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Title | A New SARS-CoV-2 Dual-Purpose Serology Test: Highly Accurate Infection Tracing and Neutralizing Antibody Response Detection |
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