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Interindividual Immunogenic Variants: Susceptibility to Coronavirus, Respiratory Syncytial Virus and Influenza Virus Publisher Pubmed



Darbeheshti F1, 2 ; Mahdiannasser M1 ; Uhal BD3 ; Ogino S4, 5, 6 ; Gupta S7 ; Rezaei N8, 9, 10
Authors
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Authors Affiliations
  1. 1. Department of Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Medical Genetics Network (MeGeNe), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  3. 3. Department of Physiology, Michigan State University, East Lansing, MI, United States
  4. 4. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, United States
  5. 5. Department of Oncologic Pathology, Dana-Farber Cancer Institute, Boston, MA, United States
  6. 6. Cancer Immunology and Cancer Epidemiology Programs, Dana-Farber Harvard Cancer Center, Boston, MA, United States
  7. 7. Division of Basic and Clinical Immunology, Department of Medicine, University of California, Irvine, CA, United States
  8. 8. Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  10. 10. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran

Source: Reviews in Medical Virology Published:2021


Abstract

The coronavirus disease (Covid-19) pandemic is the most serious event of the year 2020, causing considerable global morbidity and mortality. The goal of this review is to provide a comprehensive summary of reported associations between inter-individual immunogenic variants and disease susceptibility or symptoms caused by the coronavirus strains severe acute respiratory syndrome-associated coronavirus, severe acute respiratory syndrome-associated coronavirus-2, and two of the main respiratory viruses, respiratory syncytial virus and influenza virus. The results suggest that the genetic background of the host could affect the levels of proinflammatory and anti-inflammatory cytokines and might modulate the progression of Covid-19 in affected patients. Notably, genetic variations in innate immune components such as toll-like receptors and mannose-binding lectin 2 play critical roles in the ability of the immune system to recognize coronavirus and initiate an early immune response to clear the virus and prevent the development of severe symptoms. This review provides promising clues related to the potential benefits of using immunotherapy and immune modulation for respiratory infectious disease treatment in a personalized manner. © 2021 John Wiley & Sons Ltd.
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