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COVID-19 Serology in New York State Using a Multiplex Microsphere Immunoassay
Danielle T. Hunt; Jennifer L. Yates; Karen E. Kulas; Kyle Carson; Theresa Lamson; Valerie Demarest; Andrea Furuya; Kelly Howard; Mary Marchewka; Randy Stone; Heidi Tucker; Casey Warszycki; Jim Yee; He S. Yang; Sabrina Racine-Brzostek; Zhen Zhao; Monir Ejemel; Qi Li; Yang Wang; Sebastian Fernando; Francesca La Carpia; Eldad A. Hod; Kathleen A. McDonough; William T. Lee.
Afiliação
  • Danielle T. Hunt; Wadsworth Center/New York State Department of Health
  • Jennifer L. Yates; Wadsworth Center/New York State Department of Health
  • Karen E. Kulas; Wadsworth Center/New York State Department of Health
  • Kyle Carson; Wadsworth Center/New York State Department of Health
  • Theresa Lamson; Wadsworth Center/New York State Department of Health
  • Valerie Demarest; Wadsworth Center/New York State Department of Health
  • Andrea Furuya; Wadsworth Center/New York State Department of Health
  • Kelly Howard; Wadsworth Center/New York State Department of Health
  • Mary Marchewka; Wadsworth Center/New York State Department of Health
  • Randy Stone; Wadsworth Center/New York State Department of Health
  • Heidi Tucker; Wadsworth Center/New York State Department of Health
  • Casey Warszycki; Wadsworth Center/New York State Department of Health
  • Jim Yee; Weill Cornell Medicine/New York Presbyterian Hospital/Weill Cornell Medical Campus
  • He S. Yang; Weill Cornell Medicine/New York Presbyterian Hospital/Weill Cornell Medical Campus
  • Sabrina Racine-Brzostek; Weill Cornell Medicine/New York Presbyterian Hospital/Weill Cornell Medical Campus
  • Zhen Zhao; Weill Cornell Medicine/New York Presbyterian Hospital/Weill Cornell Medical Campus
  • Monir Ejemel; MassBiologics of the University of Massachusetts Medical School
  • Qi Li; MassBiologics of the University of Massachusetts Medical School
  • Yang Wang; MassBiologics of the University of Massachusetts Medical School
  • Sebastian Fernando; Columbia University Irving Medical Center
  • Francesca La Carpia; Columbia University Irving Medical Center
  • Eldad A. Hod; Columbia University Irving Medical Center
  • Kathleen A. McDonough; Wadsworth Center/New York State Department of Health
  • William T. Lee; Wadsworth Center/New York State Department of Health
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21257125
ABSTRACT
The emergence of SARS-CoV-2, leading to COVID-19, necessitated the development of new molecular and serological tests. Here, we describe a multiplexed serological assay developed as the global pandemic moved into New York State in the spring of 2020. The original microsphere immunoassay used a target antigen from the SARS-CoV-1 virus responsible for the 2003 SARS outbreak, but evolved to incorporate multiple SARS-CoV-2 protein antigens (nucleocapsid, spike and spike domains, spike and nucleocapsid proteins from seasonal human coronaviruses). Besides being highly versatile due to multiplex capabilities, the assay was highly specific and sensitive and adaptable to measuring both total antibodies and antibody isotypes. While determining the assay performance characteristics, we were able to identify antibody production patterns (e.g., kinetics of isotypes, individual variations) for total antibodies and individual antibody classes. Overall, the results provide insights into the laboratory response to new serology needs, and how the evolution and fine-tuning of a serology assay helped contribute to a better understanding of the antibody response to SARS-CoV-2.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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