Publication

Neutralizing antibody: a savior in the Covid-19 disease

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Last modified
  • 05/22/2025
Type of Material
Authors
    Sneh Lata Gupta, Emory UniversityRishi Kumar Jaiswal, Loyola University Health System
Language
  • English
Date
  • 2022-03-01
Publisher
  • Emory University Libraries
Publication Version
Copyright Statement
  • © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 49
Issue
  • 3
Start Page
  • 2465
End Page
  • 2474
Grant/Funding Information
  • The author(s) received no financial support for the authorship, and/or publication of this article.
Supplemental Material (URL)
Abstract
  • Coronavirus outbreak was declared a pandemic by World Health Organization (WHO) in March 2020. The pandemic has led to a devastating loss of life. It has shown us how infectious diseases can cause human existence at stake, and community health is important. The spike protein is the most immunogenic component of the virus. Most vaccine development strategies have focused on the receptor-binding domain (RBD) in the spike protein because it is the most specific target site that recognizes and interacts with human lung cells. Neutralizing antibodies are generated by the humoral immune system and reduce the viral load by binding to spike protein components. Neutralizing antibodies are the proteins secreted by plasma cells and serve as an important part of the defense mechanism. In the recent Covid-19 infection, neutralizing antibodies can be utilized for both diagnostic such as immune surveillance and therapeutic tools such as plasma therapy. So far, many monoclonal antibodies are in the clinical trial phase, and few of them are already in use. In this review, we have discussed details about neutralizing antibodies and their role in combating Covid-19 disease.
Author Notes
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Medicine and Surgery

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