International Journal of Molecular Sciences (Aug 2021)

Severe COVID-19 Patients Show an Increase in Soluble TNFR1 and ADAM17, with a Relationship to Mortality

  • Yadira Palacios,
  • Andy Ruiz,
  • Lucero A. Ramón-Luing,
  • Ranferi Ocaña-Guzman,
  • Omar Barreto-Rodriguez,
  • Anahí Sánchez-Monciváis,
  • Brenda Tecuatzi-Cadena,
  • Ana G. Regalado-García,
  • Rey David Pineda-Gudiño,
  • Alicia García-Martínez,
  • Fortunato Juárez-Hernández,
  • Juan Pablo Farias-Contreras,
  • Ingrid Fricke-Galindo,
  • Gloria Pérez-Rubio,
  • Ramcés Falfán-Valencia,
  • Ivette Buendia-Roldan,
  • Karen Medina-Quero,
  • Leslie Chavez-Galan

DOI
https://doi.org/10.3390/ijms22168423
Journal volume & issue
Vol. 22, no. 16
p. 8423

Abstract

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Overproduction of inflammatory cytokines is a keystone event in COVID-19 pathogenesis; TNF and its receptors (TNFR1 and TNFR2) are critical pro-inflammatory molecules. ADAM17 releases the soluble (sol) forms of TNF, TNFR1, and TNFR2. This study evaluated TNF, TNFRs, and ADAM17 at the protein, transcriptional, and gene levels in COVID-19 patients with different levels of disease severity. In total, 102 patients were divided into mild, moderate, and severe condition groups. A group of healthy donors (HD; n = 25) was included. Our data showed that solTNFR1 and solTNFR2 were elevated among the COVID-19 patients (p p p p = 0.006, Rho = −0.33). The solADAM17 level was higher in severe as compared to mild disease conditions (p p TNFRSF1A:rs767455 and a severe degree of disease was suggested. These data suggest that solTNFR1 and solADAM17 are increased in severe conditions. solTNFR1 should be considered a potential target in the development of new therapeutic options.

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