Respiratory Research (Nov 2023)

COVID-19 induces more pronounced extracellular matrix deposition than other causes of ARDS

  • Natália de Souza Xavier Costa,
  • Gabriel Ribeiro Júnior,
  • Ellen Caroline Toledo do Nascimento,
  • Jôse Mara de Brito,
  • Leila Antonangelo,
  • Caroline Silvério Faria,
  • Jhonatas Sirino Monteiro,
  • João Carlos Setubal,
  • João Renato Rebello Pinho,
  • Roberta Verciano Pereira,
  • Marilia Seelaender,
  • Gabriela Salim de Castro,
  • Joanna D. C. C. Lima,
  • Renata Aparecida de Almeida Monteiro,
  • Amaro Nunes Duarte-Neto,
  • Paulo Hilário Nascimento Saldiva,
  • Luiz Fernando Ferraz da Silva,
  • Marisa Dolhnikoff,
  • Thais Mauad

DOI
https://doi.org/10.1186/s12931-023-02555-7
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 11

Abstract

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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.

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