CD45: a critical regulator in immune cells to predict severe and non-severe COVID-19 patients

Aging (Albany NY). 2020 Oct 16;12(20):19867-19879. doi: 10.18632/aging.103941. Epub 2020 Oct 16.

Abstract

The ongoing outbreak of COVID-19 has been announced by the World Health Organization as a worldwide public health emergency. The aim of this study was to distinguish between severe and non-severe patients in early diagnosis. The results showed that the mortality of COVID-19 patients increased accompanied by age. Host factors CRP, IL-1β, hs-CRP, IL-8, and IL-6 levels in severe pneumonia patients were higher than in non-severe patients. CD3, CD8, and CD45 counts were decreased in COVID-19 patients. The results of this study suggest that the K-values of CD45 might be useful in distinguishing between severe and non-severe cases. The cut-off value for CD45 was -94.33. The K-values for CD45 in non-severe case were above the cut-off values, indicating a 100% prediction success rate for severe and non-severe cases following SARS-CoV-2 infection. The results confirmed that immune system dysfunction is a potential cause of mortality following COVID-19 infection, particularly for the elderly. CD45 deficiency dysfunction the naïve and memory T lymphocytes which may affects the long-term effectiveness of COVID-19 vaccines. K-values of CD45 might be useful in distinguishing between severe and non-severe cases in the early infection. May be CD45 could increase the diagnostic sensitivity.

Keywords: COVID-19; clinical characteristics; coronavirus disease 2019; immunopathology; pneumonia; severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Betacoronavirus / immunology*
  • CD3 Complex / deficiency*
  • COVID-19
  • Coronavirus Infections / blood
  • Coronavirus Infections / diagnosis
  • Coronavirus Infections / immunology*
  • Coronavirus Infections / virology
  • Early Diagnosis
  • Female
  • Host-Pathogen Interactions / immunology*
  • Humans
  • Leukocyte Common Antigens / deficiency*
  • Male
  • Middle Aged
  • Pandemics
  • Pneumonia, Viral / blood
  • Pneumonia, Viral / diagnosis
  • Pneumonia, Viral / immunology*
  • Pneumonia, Viral / virology
  • Retrospective Studies
  • SARS-CoV-2
  • Young Adult

Substances

  • CD3 Complex
  • Leukocyte Common Antigens
  • PTPRC protein, human