4.7 Article

Pathological post-mortem findings in lungs infected with SARS-CoV-2

Journal

JOURNAL OF PATHOLOGY
Volume 253, Issue 1, Pages 31-40

Publisher

WILEY
DOI: 10.1002/path.5549

Keywords

SARS-CoV-2; coronavirus; COVID-19; lung; infection; ACE2; TMPRSS2

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Italy was the first European nation to be heavily affected by SARS-CoV-2, with over 33,000 deaths recorded by the end of May 2020. Autopsies on nine patients who died of SARS-CoV-2-associated disease revealed diffuse alveolar damage in lung tissues, with vascular involvement and eosinophilic infiltrate. The presence of SARS-CoV-2 viral RNA in the lung tissues of all nine patients was also confirmed.
Italy was the first European nation to be massively infected by SARS-CoV-2. Up to the end of May 2020, more than 33,000 deaths had been recorded in Italy, with a large prevalence among males, those over 75 years of age, and in association with co-morbidities. We describe the lung pathological and immunohistochemical post-mortem findings at the autopsy of nine patients who died of SARS-CoV-2-associated disease. We found in the lung tissues of all patients histological changes consistent with diffuse alveolar damage in various evolution phases ranging from acute exudative to acute proliferative to fibrotic phase. Alveolar damage was associated with prominent involvement of the vascular component in both the interstitial capillaries and the mid-size vessels, with capillary fibrin micro-thrombi, as well as organized thrombi even in medium-sized arteries, in most cases not related to sources of embolism. Eosinophilic infiltrate was also seen, probably reactive to pharmacological treatment. Viral RNA of SARS-CoV-2 was detected from the lung tissues of all the nine patients. Immunohistochemistry for the receptor of the SARS-CoV-2, ACE2, and its priming activator TMPRSS2 revealed that both proteins co-localize in airway cells. In particular, the ACE2 protein was expressed in both endothelial cells and alveolar type I and II pneumocytes in the areas of histological diffuse alveolar damage (DAD). Pneumocytes, but not endothelial cells, also expressed TMPRSS2. There are no distinctive histological features of SARS-CoV-2 infection with respect to SARS-CoV-1 and other DAD with different aetiology. The identification of the cause of death in the course of SARS-CoV-2 infection is more likely multi-factorial. (c) 2020 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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