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Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2.
Williams, Erin; Colson, Jordan; Valiathan, Ranjini; Carreño, Juan Manuel; Krammer, Florian; Hoffer, Michael; Pallikkuth, Suresh; Pahwa, Savita; Andrews, David.
  • Williams E; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL 33136, USA; Department of Biomedical Engineering, University of Miami, Miami, FL 33136, USA.
  • Colson J; Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
  • Valiathan R; Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
  • Carreño JM; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Center for Vaccine Research and Pandemic Preparedness (C-VARPP), Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Krammer F; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Department of Pathology, Molecular and Cell-based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Center for Vaccine Research and Pandemic Preparedness (C-VARPP), Icahn School of
  • Hoffer M; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL 33136, USA; Department of Neurological Surgery, University of Miami, Miller School of Medicine, Miami, FL 33136, USA.
  • Pallikkuth S; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
  • Pahwa S; Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL 33136, USA. Electronic address: spahwa@med.miami.edu.
  • Andrews D; Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA. Electronic address: dandrews@miami.edu.
Vaccine ; 40(41): 5868-5872, 2022 09 29.
Article in English | MEDLINE | ID: covidwho-2004592
ABSTRACT

BACKGROUND:

Breakthrough infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) has occurred in populations with high vaccination rates.

METHODS:

In a longitudinal cohort study, pre-breakthrough infection sera for Omicron breakthroughs (n = 12) were analyzed. Assays utilized include a laboratory-developed solid phase binding assay to recombinant spike protein, a commercial assay to the S1 domain of the spike protein calibrated to the World Health Organization (WHO) standard, and a commercial solid-phase surrogate neutralizing activity (SNA) assay. All assays employed spike protein preparations based on sequences from the Wuhan-Hu-1 strain.

RESULTS:

Pre-breakthrough binding antibody titers ranged from 1800 to 151,200 for the laboratory-developed binding assay, which correlated well and agreed quantitatively with the commercial spike S1 domain WHO calibrated assay. SNA was detected in 10/12 (83%) samples.

CONCLUSIONS:

Neither high binding titers nor SNA were markers of protection from Omicron infection/re-infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Vaccine Year: 2022 Document Type: Article Affiliation country: J.vaccine.2022.08.058

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Vaccine Year: 2022 Document Type: Article Affiliation country: J.vaccine.2022.08.058