Author:
de Souza Xavier Costa Natália,Ribeiro Júnior Gabriel,do Nascimento Ellen Caroline Toledo,de Brito Jôse Mara,Antonangelo Leila,Faria Caroline Silvério,Monteiro Jhonatas Sirino,Setubal João Carlos,Pinho João Renato Rebello,Pereira Roberta Verciano,Seelaender Marilia,de Castro Gabriela Salim,Lima Joanna D. C. C.,de Almeida Monteiro Renata Aparecida,Duarte-Neto Amaro Nunes,Saldiva Paulo Hilário Nascimento,Ferraz da Silva Luiz Fernando,Dolhnikoff Marisa,Mauad Thais
Abstract
Abstract
Background
Lung fibrosis is a major concern in severe COVID-19 patients undergoing mechanical ventilation (MV). Lung fibrosis frequency in post-COVID syndrome is highly variable and even if the risk is proportionally small, many patients could be affected. However, there is still no data on lung extracellular matrix (ECM) composition in severe COVID-19 and whether it is different from other aetiologies of ARDS.
Methods
We have quantified different ECM elements and TGF-β expression in lung tissue of 28 fatal COVID-19 cases and compared to 27 patients that died of other causes of ARDS, divided according to MV duration (up to six days or seven days or more). In COVID-19 cases, ECM elements were correlated with lung transcriptomics and cytokines profile.
Results
We observed that COVID-19 cases presented significant increased deposition of collagen, fibronectin, versican, and TGF-β, and decreased decorin density when compared to non-COVID-19 cases of similar MV duration. TGF-β was precociously increased in COVID-19 patients with MV duration up to six days. Lung collagen was higher in women with COVID-19, with a transition of upregulated genes related to fibrillogenesis to collagen production and ECM disassembly along the MV course.
Conclusions
Fatal COVID-19 is associated with an early TGF-β expression lung environment after the MV onset, followed by a disordered ECM assembly. This uncontrolled process resulted in a prominent collagen deposition when compared to other causes of ARDS. Our data provides pathological substrates to better understand the high prevalence of pulmonary abnormalities in patients surviving COVID-19.
Funder
Fundação Bill e Melinda Gates, Estados Unidos
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Fundação de Amparo à Pesquisa do Estado de São Paulo, Brasil
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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