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Titers of antibodies against ancestral SARS-CoV-2 correlate with levels of neutralizing antibodies to multiple variants.
Tran, Trung The; Vaage, Eline Benno; Mehta, Adi; Chopra, Adity; Tietze, Lisa; Kolderup, Anette; Anthi, Aina; König, Marton; Nygaard, Gro; Lind, Andreas; Müller, Fredrik; Nissen-Meyer, Lise Sofie; Magnus, Per; Trogstad, Lill; Mjaaland, Siri; Søraas, Arne; Midtvedt, Karsten; Åsberg, Anders; Barratt-Due, Andreas; Medhus, Asle W; Høivik, Marte Lie; Lundin, Knut; Karlsen, Randi Fuglaas; Dahle, Reidun; Danielsson, Karin; Thomassen, Kristine Stien; Kro, Grete Birkeland; Cox, Rebecca J; Zhou, Fan; Langeland, Nina; Aukrust, Pål; Melum, Espen; Åvitsland, Tone Lise; Wiencke, Kristine; Holter, Jan Cato; Munthe, Ludvig A; Grødeland, Gunnveig; Andersen, Jan-Terje; Vaage, John Torgils; Lund-Johansen, Fridtjof.
  • Tran TT; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Vaage EB; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Mehta A; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Chopra A; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Tietze L; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Kolderup A; Department of Pharmacology, Oslo University Hospital, 0424, Oslo, Norway.
  • Anthi A; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • König M; Institute of Clinical Medicine, University of Oslo, 0315, Oslo, Norway.
  • Nygaard G; Department of Neurology, Oslo University Hospital, 0424, Oslo, Norway.
  • Lind A; Department of Neurology, Oslo University Hospital, 0424, Oslo, Norway.
  • Müller F; Department of Microbiology, Oslo University Hospital, 0424, Oslo, Norway.
  • Nissen-Meyer LS; Department of Microbiology, Oslo University Hospital, 0424, Oslo, Norway.
  • Magnus P; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Trogstad L; Division of Epidemiology, Norwegian Institute of Public Health, Oslo, Norway.
  • Mjaaland S; Division of Method Development and Analytics, Norwegian Institute of Public Health, Oslo, Norway.
  • Søraas A; Division of Infectious Disease Control, Section of Immunology, Norwegian Institute of Public Health, Oslo, Norway.
  • Midtvedt K; Department of Microbiology, Oslo University Hospital, 0424, Oslo, Norway.
  • Åsberg A; Department of Transplantation Medicine, Oslo University Hospital, 0424, Oslo, Norway.
  • Barratt-Due A; Department of Transplantation Medicine, Oslo University Hospital, 0424, Oslo, Norway.
  • Medhus AW; Department of Pharmacy, Oslo University, Oslo, Norway.
  • Høivik ML; Division of Emergencies and Critical Care, Oslo University Hospital, 0424, Oslo, Norway.
  • Lundin K; Department of Gastroenterology, Oslo University Hospital, 0424, Oslo, Norway.
  • Karlsen RF; Department of Gastroenterology, Oslo University Hospital, 0424, Oslo, Norway.
  • Dahle R; Institute of Clinical Medicine, University of Oslo, 0315, Oslo, Norway.
  • Danielsson K; Department of Gastroenterology, Oslo University Hospital, 0424, Oslo, Norway.
  • Thomassen KS; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Kro GB; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Cox RJ; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Zhou F; Department of Immunology, Oslo University Hospital, 0424, Oslo, Norway.
  • Langeland N; Department of Microbiology, Oslo University Hospital, 0424, Oslo, Norway.
  • Aukrust P; Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Melum E; Influenza Centre, Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Åvitsland TL; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Wiencke K; Section of Clinical Immunology and Infectious Diseases, Oslo University Hospital, Oslo, Norway.
  • Holter JC; Research Institute of Internal Medicine, Sognsvannsveien 20, Oslo University Hospital, Oslo, Norway.
  • Munthe LA; Institute of Clinical Medicine, University of Oslo, 0315, Oslo, Norway.
  • Grødeland G; Research Institute of Internal Medicine, Sognsvannsveien 20, Oslo University Hospital, Oslo, Norway.
  • Andersen JT; Norwegian PSC Research Center, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Vaage JT; Section of Gastroenterology, Department of Transplantation Medicine, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital, Oslo, Norway.
  • Lund-Johansen F; Section of Gastroenterology, Department of Transplantation Medicine, Division of Surgery, Inflammatory Diseases and Transplantation, Oslo University Hospital, Oslo, Norway.
NPJ Vaccines ; 7(1): 174, 2022 Dec 30.
Article in English | MEDLINE | ID: covidwho-2185871
ABSTRACT
Diagnostic assays currently used to monitor the efficacy of COVID-19 vaccines measure levels of antibodies to the receptor-binding domain of ancestral SARS-CoV-2 (RBDwt). However, the predictive value for protection against new variants of concern (VOCs) has not been firmly established. Here, we used bead-based arrays and flow cytometry to measure binding of antibodies to spike proteins and receptor-binding domains (RBDs) from VOCs in 12,000 serum samples. Effects of sera on RBD-ACE2 interactions were measured as a proxy for neutralizing antibodies. The samples were obtained from healthy individuals or patients on immunosuppressive therapy who had received two to four doses of COVID-19 vaccines and from COVID-19 convalescents. The results show that anti-RBDwt titers correlate with the levels of binding- and neutralizing antibodies against the Alpha, Beta, Gamma, Delta, Epsilon and Omicron variants. The benefit of multiplexed analysis lies in the ability to measure a wide range of anti-RBD titers using a single dilution of serum for each assay. The reactivity patterns also yield an internal reference for neutralizing activity and binding antibody units per milliliter (BAU/ml). Results obtained with sera from vaccinated healthy individuals and patients confirmed and extended results from previous studies on time-dependent waning of antibody levels and effects of immunosuppressive agents. We conclude that anti-RBDwt titers correlate with levels of neutralizing antibodies against VOCs and propose that our method may be implemented to enhance the precision and throughput of immunomonitoring.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines / Variants Language: English Journal: NPJ Vaccines Year: 2022 Document Type: Article Affiliation country: S41541-022-00586-7

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines / Variants Language: English Journal: NPJ Vaccines Year: 2022 Document Type: Article Affiliation country: S41541-022-00586-7