PLoS ONE (Jan 2021)

Angiotensin II receptor I auto-antibodies following SARS-CoV-2 infection.

  • Yonghou Jiang,
  • Fergal Duffy,
  • Jennifer Hadlock,
  • Andrew Raappana,
  • Sheila Styrchak,
  • Ingrid Beck,
  • Fred D Mast,
  • Leslie R Miller,
  • William Chour,
  • John Houck,
  • Blair Armistead,
  • Venkata R Duvvuri,
  • Winnie Yeung,
  • Micaela Haglund,
  • Jackson Wallner,
  • Julie A Wallick,
  • Samantha Hardy,
  • Alyssa Oldroyd,
  • Daisy Ko,
  • Ana Gervassi,
  • Kim M Murray,
  • Henry Kaplan,
  • John D Aitchison,
  • James R Heath,
  • D Noah Sather,
  • Jason D Goldman,
  • Lisa Frenkel,
  • Whitney E Harrington

DOI
https://doi.org/10.1371/journal.pone.0259902
Journal volume & issue
Vol. 16, no. 11
p. e0259902

Abstract

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BackgroundCoronavirus disease 2019 (COVID-19) is associated with endothelial activation and coagulopathy, which may be related to pre-existing or infection-induced pro-thrombotic autoantibodies such as those targeting angiotensin II type I receptor (AT1R-Ab).MethodsWe compared prevalence and levels of AT1R-Ab in COVID-19 cases with mild or severe disease to age and sex matched negative controls utilizing multivariate logistic and quantile regression adjusted for comorbidities including hypertension, diabetes, and heart disease.ResultsThere were trends toward increased prevalence (50% vs. 33%, p = 0.1) and level of AT1R-Ab (median 9.8 vs. 6.1 U/mL, p = 0.06) in all cases versus controls. When considered by COVID-19 disease severity, there was a trend toward increased prevalence of AT1R-Ab (55% vs. 31%, p = 0.07), as well as significantly higher AT1R-Ab levels (median 10.7 vs. 5.9 U/mL, p = 0.03) amongst individuals with mild COVID-19 versus matched controls. In contrast, the prevalence (42% vs. 37%, p = 0.9) and level (both medians 6.7 U/mL, p = 0.9) of AT1R-Ab amongst those with severe COVID-19 did not differ from matched controls.ConclusionsThese findings support an association between COVID-19 and AT1R-Ab, emphasizing that vascular pathology may be present in individuals with mild COVID-19 as well as those with severe disease.