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Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19

Maximilian Ackermann; Stijn E. Verleden; Mark Kuehnel; Axel Haverich; Tobias Welte; Florian Laenger; Arno Vanstapel; Christopher Werlein · New England Journal of Medicine · 2020

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BACKGROUND: Progressive respiratory failure is the primary cause of death in the coronavirus disease 2019 (Covid-19) pandemic. Despite widespread interest in the pathophysiology of the disease, relatively little is known about the associated morphologic and molecular changes in the peripheral lung of patients who die from Covid-19. METHODS: We examined 7 lungs obtained during autopsy from patients who died from Covid-19 and compared them with 7 lungs obtained during autopsy from patients who died from acute respiratory distress syndrome (ARDS) secondary to influenza A(H1N1) infection and 10 age-matched, uninfected control lungs. The lungs were studied with the use of seven-color immunohistochemical analysis, micro-computed tomographic imaging, scanning electron microscopy, corrosion casting, and direct multiplexed measurement of gene expression. RESULTS: In patients who died from Covid-19-associated or influenza-associated respiratory failure, the histologic pattern in the peripheral lung was diffuse alveolar damage with perivascular T-cell infiltration. The lungs from patients with Covid-19 also showed distinctive vascular features, consisting of severe endothelial injury associated with the presence of intracellular virus and disrupted cell membranes. Histologic analysis of pulmonary vessels in patients with Covid-19 showed widespread thrombosis with microangiopathy. Alveolar capillary microthrombi were 9 times as prevalent in patients with Covid-19 as in patients with influenza (P<0.001). In lungs from patients with Covid-19, the amount of new vessel growth - predominantly through a mechanism of intussusceptive angiogenesis - was 2.7 times as high as that in the lungs from patients with influenza (P<0.001). CONCLUSIONS: In our small series, vascular angiogenesis distinguished the pulmonary pathobiology of Covid-19 from that of equally severe influenza virus infection. The universality and clinical implications of our observations require further research to define. (Funded by the National Institutes of Health and others.).

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APA 7

Ackermann, M, Verleden, S. E, Kuehnel, M, Haverich, A, Welte, T, Laenger, F, Vanstapel, A, & Werlein, C. (2020). Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19. https://doi.org/10.1056/nejmoa2015432

MLA

Ackermann, Maximilian, et al. "Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19." 2020. https://doi.org/10.1056/nejmoa2015432.

Chicago

Ackermann, Maximilian, Stijn E. Verleden, Mark Kuehnel, Axel Haverich, Tobias Welte, Florian Laenger, Arno Vanstapel, and Christopher Werlein. 2020. "Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19.". https://doi.org/10.1056/nejmoa2015432.

Harvard

Ackermann, M. et al. 2020, Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19, New England Journal of Medicine, available at: https://doi.org/10.1056/nejmoa2015432 [Accessed 5 Aug. 2026].

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Título
Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19
Autor / colaboradores
Maximilian Ackermann; Stijn E. Verleden; Mark Kuehnel; Axel Haverich; Tobias Welte; Florian Laenger; Arno Vanstapel; Christopher Werlein
Editorial
New England Journal of Medicine
Año de publicación
2020
Idioma
Inglés

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