Elevated extracellular HSP72 and blunted heat shock response in severe covid-19 patients

• Autor(a) principal: Russo, Mariana Kras Borges
• Data de Publicação: 2022
• Outros Autores: Kowalewski, Lucas Stahlhöfer, Natividade, Gabriella Richter da, Muller, Carlos Henrique de Lemos, Schroeder, Helena Trevisan, Bock, Patricia Martins, Ayres, Layane Ramos, Cardoso, Bernardo Urbano, Boeckel, Caroline Zanotto de, Schein, Julia Tsao, Rech, Tatiana Helena, Crispim, Daisy, Canani, Luis Henrique Santos, Friedman, Rogério, Leitão, Cristiane Bauermann, Gerchman, Fernando, Krause, Maurício da Silva
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UFRGS
• Texto Completo: http://hdl.handle.net/10183/250473
• topic: COVID-19; Infecções por coronavirus; SARS-CoV-2; Inflamação; Choque séptico; Cuidados críticos; Doenças metabólicas; Inflammation; Heat shock response; HSP72; Metabolic diseases; Critically ill patients

Aims: We hypothesized that critically ill patients with SARS-CoV-2 infection and insulin resistance would present a reduced Heat Shock Response (HSR), which is a pathway involved in proteostasis and anti-inflammation, subsequently leading to worse outcomes and higher inflammation. In this work we aimed: (i) to measure the concentration of extracellular HSP72 (eHSP72) in patients with severe COVID-19 and in comparison with noninfected patients; (ii) to compare the HSR between critically ill patients with COVID-19 (with and without diabetes); and (iii) to compare the HSR in these patients with noninfected individuals. Methods: Sixty critically ill adults with acute respiratory failure with SARS-CoV-2, with or without diabetes, were selected. Noninfected subjects were included for comparison (healthy, n = 19 and patients with diabetes, n = 22). Blood samples were collected to measure metabolism (glucose and HbA1c); oxidative stress (lypoperoxidation and carbonyls); cytokine profile (IL-10 and TNF); eHSP72; and the HSR (in vitro). Results: Patients with severe COVID-19 presented higher plasma eHSP72 compared with healthy individuals and noninfected patients with diabetes. Despite the high level of plasma cytokines, no differences were found between critically ill patients with COVID-19 with or without diabetes. Critically ill patients, when compared to noninfected, presented a blunted HSR. Oxidative stress markers followed the same pattern. No differences in the HSR (extracellular/intracellular level) were found between critically ill patients, with or without diabetes. Conclusions: We demonstrated that patients with severe COVID-19 have elevated plasma eHSP72 and that their HSR is blunted, regardless of the presence of diabetes. These results might explain the uncontrolled inflammation and also provide insights on the increased risk in developing type 2 diabetes after SARS-CoV-2 infection.