1. A deficient immune response to SARS-CoV-2 in the nasopharynx is associated with severe COVID-19 pneumonia
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Carlos Pita-Martínez, Felipe Pérez-García, Ana Virseda Berdices, María Martin-Vicente, Lucía Castilla-García, Irene Hervás Fernández, Victoria González Ventosa, María José Muñoz-Gómez, Juan Cuadros-González, Jesús F Bermejo-Martin, Salvador Resino, and Isidoro Martínez
- Subjects
SARS-CoV-2 ,COVID-19 ,Pneumonia ,Gene expression ,Mucosal nasopharynx ,Immune response ,Infectious and parasitic diseases ,RC109-216 - Abstract
Objectives: We analyzed the expression of inflammatory and antiviral genes in the nasopharynx of SARS-CoV-2 infected patients and their association with the severity of COVID-19 pneumonia. Methods: We conducted a cross-sectional study on 223 SARS-CoV-2 infected patients. Clinical data were collected from medical records, and nasopharyngeal samples were collected in the first 24 hours after admission to the emergency room. The gene expression of eight proinflammatory/antiviral genes (plasminogen activator urokinase receptor [PLAUR], interleukin [IL]-6, IL-8, interferon [IFN]-β, IFN-stimulated gene 15 [ISG15], retinoic acid-inducible gene I [RIG-I], C-C motif ligand 5 [CCL5], and chemokine C-X-C motif ligand 10 [CXCL10]) were quantified by real-time polymerase chain reaction. Outcome variables were: (i) pneumonia; (ii) severe pneumonia or acute respiratory distress syndrome. Statistical analysis was performed using multivariate logistic regression analyses. Results: We enrolled 84 mild, 88 moderate, and 51 severe/critical cases. High expression of PLAUR (adjusted odds ratio [aOR] = 1.25; P = 0.032, risk factor) and low expression of CXCL10 (aOR = 0.89; P = 0.048, protective factor) were associated with pneumonia. Furthermore, lower values of ISG15 (aOR = 0.88, P = 0.021), RIG-I (aOR = 0.87, P = 0.034), CCL5 (aOR = 0.73, P
- Published
- 2023
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