| Literature DB >> 33215858 |
Abigail Vanderheiden1,2,3, Venkata Viswanadh Edara1,2,3, Katharine Floyd1,2,3, Robert C Kauffman2,4, Grace Mantus2,4, Evan Anderson1, Nadine Rouphael2,5, Sri Edupuganti2,5, Pei-Yong Shi6, Vineet D Menachery7, Jens Wrammert2,4, Mehul S Suthar1,2,3.
Abstract
SARS-CoV-2 is a recently emerged human coronavirus that has escalated to a pandemic. There are currently no approved vaccines for SARS-CoV-2, which causes severe respiratory illness or death. Defining the antibody response to SARS-CoV-2 will be essential for understanding disease progression, long-term immunity, and vaccine efficacy. Here we describe two methods for evaluating the neutralization capacity of SARS-CoV-2 antibodies. The basic protocol is a focus reduction neutralization test (FRNT), which involves immunostaining infected cells with a chromogen deposit readout. The alternate protocol is a modification of the FRNT that uses an infectious clone-derived SARS-CoV-2 virus expressing a fluorescent reporter. These protocols are adapted for use in a high-throughput setting, and are compatible with large-scale vaccine studies or clinical testing.Entities:
Keywords: SARS-Cov-2; antibody neutralization; high-throughput neutralization assay; neutralizing antibodies; serological assay
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Year: 2020 PMID: 33215858 PMCID: PMC7864545 DOI: 10.1002/cpim.116
Source DB: PubMed Journal: Curr Protoc Immunol ISSN: 1934-3671