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The Usefulness of Rare Blood Group Systems in the Risk Determination for Severe COVID-19.

Theocharis G KonstantinidisValeria IliadiGeorges MartinisMaria Panopoulou
Published in: Pathophysiology : the official journal of the International Society for Pathophysiology (2021)
The newly identified human coronavirus was named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), based on a detailed analysis of clinical manifestation. It was reported that blood type O individuals were less likely to become infected by SARS-CoV, while blood type A individuals have an increased risk of severe illness. The Forssman antigen, or Forssman glycolipid synthase (FS), was first described in 1911 by John Frederick Forssman. Blood type A/B glycosyltransferases (AT/BTs) and Forssman glycolipid synthase (FS) are encoded by the evolutionarily related ABO (A/B alleles) and GBGT1 genes. In this article, based on published studies about the pathogenesis of the COVID-19, we hypothesize the possible relationship between the COVID-19 infection and rare blood type systems, such as the Forssman antigen system.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • coronavirus disease
  • endothelial cells
  • systematic review
  • randomized controlled trial
  • gene expression
  • dna methylation
  • transcription factor