Antibody Response to Symptomatic Infection With SARS‐CoV‐2 Omicron Variant Viruses, December 2021–June 2022

Author:

Sandford Ryan123ORCID,Yadav Ruchi1,Noble Emma K.12,Sumner Kelsey1ORCID,Joshi Devyani1,Tartof Sara Y.45,Wernli Karen J.6,Martin Emily T.7ORCID,Gaglani Manjusha89,Zimmerman Richard K.10,Talbot H. Keipp11,Grijalva Carlos G.11,Belongia Edward A.12ORCID,Carlson Christina1,Coughlin Melissa1,Flannery Brendan1,Pearce Brad3,Rogier Eric1

Affiliation:

1. Centers for Disease Control and Prevention Atlanta Georgia USA

2. Oak Ridge Institute for Science and Education Oak Ridge Tennessee USA

3. Rollins School of Public Health Atlanta Georgia USA

4. Department of Research & Evaluation Kaiser Permanente Southern California Yorba Linda California USA

5. Department of Health Systems Science Kaiser Permanente Bernard J. Tyson School of Medicine Pasadena California USA

6. Kaiser Permanente Washington Health Research Institute Seattle Washington USA

7. University of Michigan School of Public Health Ann Arbor Michigan USA

8. Baylor Scott & White Health Temple Texas USA

9. Texas A&M University College of Medicine Temple Texas USA

10. University of Pittsburgh Pittsburgh Pennsylvania USA

11. Vanderbilt University Medical Center Nashville Tennessee USA

12. Marshfield Clinic Research Institute Marshfield Wisconsin USA

Abstract

ABSTRACTWe describe humoral immune responses in 105 ambulatory patients with laboratory‐confirmed SARS‐CoV‐2 Omicron variant infection. In dried blood spot (DBS) collected within 5 days of illness onset and during convalescence, we measured binding antibody (bAb) against ancestral spike protein receptor binding domain (RBD) and nucleocapsid (N) protein using a commercial multiplex bead assay. Geometric mean bAb concentrations against RBD increased by a factor of 2.5 from 1258 to 3189 units/mL and by a factor of 47 against N protein from 5.5 to 259 units/mL between acute illness and convalescence; lower concentrations were associated with greater geometric mean ratios. Paired DBS specimens may be used to evaluate humoral response to SARS‐CoV‐2 infection.

Funder

Centers for Disease Control and Prevention

National Institutes of Health

Publisher

Wiley

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