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

Эндотелиит сосудов легких, тромбоз и ангиогенез при Covid-19
Axel Haverich, Alexandar Tzankov, Tobias Welte, Danny Jonigk, Maximilian Ackermann, Florian Laenger, Steven J. Mentzer, Stijn E. Verleden, Mark Kuehnel, Arno Vanstapel, Christopher Werlein, Helge Stark, William W. Li, Vincent W. Li
2020-05-21

alveolar capillary microthrombiintussusceptive angiogenesismicroangiopathypulmonary endothelialitispulmonary thrombosis
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.).
1
Alveolar capillary microthrombi were 9 times more prevalent in Covid-19 lungs than in influenza lungs (P<0.001).
2
Both Covid-19 and influenza-associated fatal respiratory failure showed diffuse alveolar damage with perivascular T-cell infiltration in peripheral lung tissue.
3
Covid-19 lungs exhibited severe endothelial injury, intracellular virus, disrupted endothelial membranes, widespread thrombosis, and pulmonary microangiopathy.
4
Enhanced vascular angiogenesis distinguished Covid-19 pulmonary pathology from equally severe influenza infection, although the findings require further research because of the small series.
5
New vessel growth was 2.7 times greater in Covid-19 than influenza lungs, predominantly through intussusceptive angiogenesis (P<0.001).

Pulmonary vasculature and peripheral lung tissue of patients who died from Covid-19

Pulmonary vascular endothelial injury, thrombosis with microangiopathy, and intussusceptive angiogenesis

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2020-05-21
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Axel Haverich
Alexandar Tzankov
Tobias Welte
Danny Jonigk
Maximilian Ackermann
Florian Laenger
Steven J. Mentzer
Stijn E. Verleden
Mark Kuehnel
Arno Vanstapel
Christopher Werlein
Helge Stark
William W. Li
Vincent W. Li
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