Multiplex Detection of Antibody Landscapes to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)/Influenza/Common Human Coronaviruses Following Vaccination or Infection With SARS-CoV-2 and Influenza

Author:

Li Zhu Nan1,Liu Feng1,Jefferson Stacie1,Horner Lauren1,Carney Paul1,Johnson Michael D L2,King Jennifer P3,Martin Emily T4,Zimmerman Richard K5,Wernli Karen6,Gaglani Manjusha78,Thompson Mark1,Flannery Brendan1,Stevens James1,Tumpey Terrence1,Levine Min Z1

Affiliation:

1. Influenza Division, Centers for Disease Control and Prevention , Atlanta, Georgia , USA

2. Department of Immunobiology, BIO5 Institute, Valley Fever Center for Excellence, and Asthma and Airway Disease Research Center, University of Arizona , Tucson, Arizona , USA

3. Marshfield Clinic Research Institute , Marshfield, Wisconsin , USA

4. University of Michigan School of Public Health , Ann Arbor, Michigan , USA

5. University of Pittsburgh, Schools of Health Sciences , Pittsburgh, Pennsylvania , USA

6. Kaiser Permanente Washington Health Research Institute , Seattle, Washington , USA

7. Baylor Scott & White Health , Temple, Texas , USA

8. Texas A&M University University College of Medicine , Temple, Texas , USA

Abstract

Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses continue to co-circulate, representing 2 major public health threats from respiratory infections with similar clinical presentations. SARS-CoV-2 and influenza vaccines can also now be co-administered. However, data on antibody responses to SARS-CoV-2 and influenza coinfection and vaccine co-administration remain limited. Methods We developed a 41-plex antibody immunity assay that can simultaneously characterize antibody landscapes to SARS-CoV-2/influenza/common human coronaviruses. We analyzed sera from 840 individuals (11–93 years), including sera from reverse transcription–polymerase chain reaction (RT-PCR)–confirmed SARS-CoV-2–positive (n = 218) and –negative (n = 120) cases, paired sera from SARS-CoV-2 vaccination (n = 29) and infection (n = 11), and paired sera from influenza vaccination (n = 56) and RT-PCR–confirmed influenza infection (n = 158) cases. Last, we analyzed sera collected from 377 individuals who exhibited acute respiratory illness (ARI) in 2020. Results This 41-plex assay has high sensitivity and specificity in detecting SARS-CoV-2 infections. It differentiated SARS-CoV-2 vaccination (antibody responses only to spike protein) from infection (antibody responses to both spike and nucleoprotein). No cross-reactive antibodies were induced to SARS-CoV-2 from influenza vaccination and infection, and vice versa, suggesting no interaction between SARS-CoV-2 and influenza antibody responses. However, cross-reactive antibodies were detected between spike proteins of SARS-CoV-2 and common human coronaviruses that were removed by serum adsorption. Among 377 individuals who exhibited ARI in 2020, 129 were influenza positive; none had serological evidence of SARS-CoV-2/influenza coinfections. Conclusions Multiplex detection of antibody landscapes can provide in-depth analysis of the antibody protective immunity to SARS-CoV-2 in the context of other respiratory viruses, including influenza.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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