Published online Apr 6, 2023. doi: 10.12998/wjcc.v11.i10.2168
Peer-review started: December 7, 2022
First decision: January 5, 2023
Revised: January 17, 2023
Accepted: March 10, 2023
Article in press: March 10, 2023
Published online: April 6, 2023
Processing time: 113 Days and 3.2 Hours
The purpose of this study was to investigate the clinical application of severe acute respiratory distress syndrome coronavirus-2 (SARS-CoV-2) specific antibody detection and anti-SARS-CoV-2 specific monoclonal antibodies (mAbs) in the treatment of coronavirus infectious disease 2019 (COVID-19). The dynamic changes of SARS-CoV-2 specific antibodies during COVID-19 were studied. Immunoglobulin M (IgM) appeared earlier and lasted for a short time, while immunoglobulin G (IgG) appeared later and lasted longer. IgM tests can be used for early diagnosis of COVID-19, and IgG tests can be used for late diagnosis of COVID-19 and identification of asymptomatic infected persons. The combination of antibody testing and nucleic acid testing, which complement each other, can improve the diagnosis rate of COVID-19. Monoclonal anti-SARS-CoV-2 specific antibodies can be used to treat hospitalized severe and critically ill patients and non-hospitalized mild to moderate COVID-19 patients. COVID-19 convalescent plasma, highly concentrated immunoglobulin, and anti-SARS-CoV-2 specific mAbs are examples of anti-SARS-CoV-2 antibody products. Due to the continuous emergence of mutated strains of the novel coronavirus, especially omicron, its immune escape ability and infectivity are enhanced, making the effects of authorized products reduced or invalid. Therefore, the optimal application of anti-SARS-CoV-2 antibody products (especially anti-SARS-CoV-2 specific mAbs) is more effective in the treatment of COVID-19 and more conducive to patient recovery.
Core Tip: Immunoglobulin M testing can be used for early diagnosis of coronavirus infectious disease 2019 (COVID-19). Immunoglobulin G testing can be used for the late diagnosis of COVID-19 and the identification of asymptomatic patients. The combination of antibody and nucleic acid testing has improved the diagnosis rate of COVID-19. The continuous emergence of mutated strains of the novel coronavirus, especially omicron, enhances its immune escape ability and infectivity, making the effects of authorized products reduced or invalid. The specific monoclonal antibodies against severe acute respiratory distress syndrome coronavirus-2 authorized by the United States Food and Drug Administration are more beneficial for the treatment of COVID-19 and patient recovery.