key: cord-0707774-3yqgou2v
authors: Babkina, Anastasiya S.; Ostrova, Irina V.; Yadgarov, Mikhail Ya; Kuzovlev, Artem N.; Grechko, Andrey V.; Volkov, Alexey V.; Golubev, Arkady M.
title: The Role of Von Willebrand Factor in the Pathogenesis of Pulmonary Vascular Thrombosis in COVID-19
date: 2022-01-21
journal: Viruses
DOI: 10.3390/v14020211
sha: de59dbd6c606505f2c97678332b23ab58c119d16
doc_id: 707774
cord_uid: 3yqgou2v

The increased plasma levels of von Willebrand factor (VWF) in patients with COVID-19 was reported in many studies, and its correlation with disease severity and mortality suggest its important role in the pathogenesis of thrombosis in COVID-19. We performed histological and immunohistochemical studies of the lungs of 29 patients who died from COVID-19. We found a significant increase in the intensity of immunohistochemical reaction for VWF in the pulmonary vascular endothelium when the disease duration was more than 10 days. In the patients who had thrombotic complications, the VWF immunostaining in the pulmonary vascular endothelium was significantly more intense than in nonsurvivors without thrombotic complications. Duration of disease and thrombotic complications were found to be independent predictors of increased VWF immunostaining in the endothelium of pulmonary vessels. We also revealed that bacterial pneumonia was associated with increased VWF staining intensity in pulmonary arterial, arteriolar, and venular endothelium, while lung ventilation was an independent predictor of increased VWF immunostaining in arterial endothelium. The results of the study demonstrated an important role of endothelial VWF in the pathogenesis of thrombus formation in COVID-19.

The novel coronavirus infection pandemic caused by SARS-CoV-2, an RNA-containing virus of the family Coronaviridae, genus Betacoronavirus, has claimed more than 5 million lives to date [1] . Despite significant progress in the treatment of the disease, several issues concerning the pathogenesis of COVID-19 remain open. The predominantly respiratory clinical manifestations of COVID-19, morphological evidence of lung damage, and respiratory failure as the most frequent cause of death suggest that the lungs are the main target organ for the SARS-CoV-2 virus.

Morphological study of internal organs of patients who died of COVID-19 shows damage and circulatory disturbances in the lungs (corresponding to acute respiratory distress syndrome) and other organs [2, 3] .

The reported complications of COVID-19 indicate the involvement of the hemostatic, central nervous, cardiovascular, and genitourinary systems in the disease mechanisms [4] [5] [6] [7] . One of the possible mechanisms contributing to extrapulmonary complications in COVID-19 is viremia, which has been identified in patients with severe infection in several studies [8, 9] .

Guidelines of the Ministry of Health of the Russian Federation, the organ specimens were fixed for 72 h in a neutral 10% formalin solution [23] . Formalin-fixed, paraffin-embedded tissues underwent standard processing to provide sections stained with hematoxylin and eosin.

The histochemical stain phosphotungstic acid-hematoxylin (PTAH) was used for fibrin detection. Weigert-van Gieson staining was used to detect elastic fibers, connective tissue, and collagen. Histological preparations were examined using a Nikon Eclipse Ni-U microscope (Nikon, Tokyo, Japan).

For immunohistochemical (IHC) study, the sections were deparaffinized in xylene and successively dehydrated in alcohol. High-temperature antigen unmasking was performed in citrate buffer, pH 6 (Target Retrieval Solution, DAKO, Glostrup, Denmark). Sections were cooled, washed 3 times in distilled water, placed in immunostaining chambers (Shandon Coverplate, Thermoscientific, Runcorn, UK), and washed with phosphate buffer (3 × 5 min) (PBS IHC Wash Buffer + Tween, Cell Marque, Rocklin, CA, USA). To suppress endogenous peroxidase activity, the sections were incubated in 3% hydrogen peroxide solution for 10 min. To prevent nonspecific binding of primary or secondary antibodies to tissue proteins, a blocking serum (Protein Block Serum-free, Abcam, Cambridge, UK) was used for 15 min. The sections were then incubated for 1 h at 37 • C with primary polyclonal antibodies against VWF (ab9378, 1:50 dilution in Antibody Diluent ab64211, Abcam, Cambridge, UK). Sections were washed with PBS (2 × 5 min). The intensity of the reaction was detected using the Mouse and Rabbit Specific HRP/DAB (ABC) Detection IHC kit (ab64264, Abcam, Cambridge, UK). After washing the sections in PBS, they were counterstained with hematoxylin. After washing in tap water, the slides were prepared using Immu-Mount water-soluble medium (Thermo Shandon, Pittsburgh, PA, USA).

After receiving digital images (10-20 images from each preparation, ×400), the intensity of IHC staining to VWF was determined using the mean optical density of the pulmonary vascular (arterial, arteriolar, venous, and venular) endothelium by the Nis-Elements BR image analysis software (Nikon, Tokyo, Japan) ( Figure 1 ). histological examination were taken in accordance with the current legislation of the Russian Federation to verify the final diagnosis and the cause of death. The study protocol was approved by the local ethics committee (№ 2/21/3). In accordance with the current Guidelines of the Ministry of Health of the Russian Federation, the organ specimens were fixed for 72 h in a neutral 10% formalin solution [23] . Formalin-fixed, paraffin-embedded tissues underwent standard processing to provide sections stained with hematoxylin and eosin. The histochemical stain phosphotungstic acid-hematoxylin (PTAH) was used for fibrin detection. Weigert-van Gieson staining was used to detect elastic fibers, connective tissue, and collagen. Histological preparations were examined using a Nikon Eclipse Ni-U microscope (Nikon, Tokyo, Japan).

For immunohistochemical (IHC) study, the sections were deparaffinized in xylene and successively dehydrated in alcohol. High-temperature antigen unmasking was performed in citrate buffer, pH 6 (Target Retrieval Solution, DAKO, Glostrup, Denmark). Sections were cooled, washed 3 times in distilled water, placed in immunostaining chambers (Shandon Coverplate, Thermoscientific, Runcorn, UK), and washed with phosphate buffer (3 × 5 min) (PBS IHC Wash Buffer + Tween, Cell Marque, Rocklin, CA, USA). To suppress endogenous peroxidase activity, the sections were incubated in 3% hydrogen peroxide solution for 10 min. To prevent nonspecific binding of primary or secondary antibodies to tissue proteins, a blocking serum (Protein Block Serum-free, Abcam, Cambridge, UK) was used for 15 min. The sections were then incubated for 1 h at 37 °C with primary polyclonal antibodies against VWF (ab9378, 1:50 dilution in Antibody Diluent ab64211, Abcam, Cambridge, UK). Sections were washed with PBS (2 × 5 min). The intensity of the reaction was detected using the Mouse and Rabbit Specific HRP/DAB (ABC) Detection IHC kit (ab64264, Abcam, Cambridge, UK). After washing the sections in PBS, they were counterstained with hematoxylin. After washing in tap water, the slides were prepared using Immu-Mount water-soluble medium (Thermo Shandon, Pittsburgh, PA, USA).

After receiving digital images (10-20 images from each preparation, ×400), the intensity of IHC staining to VWF was determined using the mean optical density of the pulmonary vascular (arterial, arteriolar, venous, and venular) endothelium by the Nis-Elements BR image analysis software (Nikon, Tokyo, Japan) ( Figure 1 ). Statistical analysis was done using the SPSS Statistics 25.0 software. Normality of data distribution was assessed using the Shapiro-Wilk and Kolmogorov-Smirnov tests with a Lilliefors correction. All patients were divided into groups: patients with duration Statistical analysis was done using the SPSS Statistics 25.0 software. Normality of data distribution was assessed using the Shapiro-Wilk and Kolmogorov-Smirnov tests with a Lilliefors correction. All patients were divided into groups: patients with duration of illness more/less than 10 days (n = 17/12, respectively); patients with thrombotic complications (n = 15) including pulmonary artery embolism (n = 7) and pulmonary artery thrombosis (n = 8), and without thrombotic complications (n = 14); patients older than/under 57 years (n = 15/14, respectively); with/without ventilatory support (n = 19/10); with/without Viruses 2022, 14, 211 4 of 13 bacterial pneumonia (n = 8/21); female/male sex (9/20) (Supplementary Materials). Cutoff points were selected based on the median value of the parameter in the sample. The duration of the disease was the sum of the length of hospital stay (from admission to death) and the number of days from the onset of symptoms to admission according to the history. Patients with an established source of thromboembolism were assigned to the group of patients with pulmonary artery embolism. Comparative intergroup analysis was performed using nonparametric Mann-Whitney U-criterion for quantitative variables and Fisher's exact test for frequencies (univariate statistical analysis). The critical level of significance was set at 0.05. Data are presented as Me (IQR), where Me is median value and IQR is the interquartile range.

To identify factors independently influencing the intensity of VWF immunostaining in the pulmonary vascular endothelium, we performed a multivariable analysis based on binary logistic regression, with estimation of the adjusted odds ratio (adj. OR) and its 95% confidence interval (CI). A stepwise inverse method (likelihood ratio) was used to include predictors in the regression model. We considered the following as potential factors influencing the increased intensity of VWF immunostaining in endothelium: duration of the disease (day 10 and more), thrombotic complications, age (57 years and older), ventilatory support, bacterial pneumonia, female sex.

Morphological study of lungs of COVID-19 nonsurvivors revealed changes typical of ARDS. At all stages of the disease, lung alterations (desquamation of bronchial and alveolar epithelium), circulatory disturbances (alveolar edema, hyaline membranes, alveolar hemorrhages, microcirculatory congestion, pulmonary vascular thrombi), along with compensatory and adaptive processes (such as fibrosis) were registered ( Figure 2 ). We found that the lung morphological changes in COVID-19 did not correlate with the stages of ARDS. Thus, fibrosis, which is not typical for the first (exudative) stage of ARDS, was detected in 50% of the patients with a disease duration of less than 10 days, which may have been due to late hospitalization or a specific pattern of fibrosis development in COVID-19. Alveolar edema, typical for the first week of ARDS, was detected in more than half of the patients after 10 days of hospitalization. In one-third of patients (8 out of 29), purulent pneumonia in the lungs was detected, indicating bacterial infection.

Patients who died before day 10 of the disease (median disease duration) had thrombotic complications in 33% of cases (4 patients out of 12). In patients with disease duration longer than 10 days, the percentage of thrombotic complications increased to 65% (11 patients out of 17); the differences were not significant (p = 0.139). Thrombotic complications included pulmonary embolism (PE) and pulmonary vascular thrombosis. A trend toward an increased incidence of pulmonary vascular thrombosis was recorded with disease duration of 10 days or more (p = 0.093). Pulmonary vascular thrombosis accounted for a major part of thrombotic complications in patients with disease duration of more than 10 days (Table 1) . Patients who died before day 10 of the disease (median disease duration) had thrombotic complications in 33% of cases (4 patients out of 12). In patients with disease duration longer than 10 days, the percentage of thrombotic complications increased to 65% (11 patients out of 17); the differences were not significant (p = 0.139). Thrombotic complications included pulmonary embolism (PE) and pulmonary vascular thrombosis. A trend toward an increased incidence of pulmonary vascular thrombosis was recorded with disease duration of 10 days or more (p = 0.093). Pulmonary vascular thrombosis accounted for a major part of thrombotic complications in patients with disease duration of more than 10 days (Table 1) . 

Positive immunoreaction for VWF was found in the endothelium of large and microcirculatory vessels, edematous fluid, and thrombi ( Figure 3 ).

Viruses 2022, 14, x FOR PEER REVIEW 6 of 13

Positive immunoreaction for VWF was found in the endothelium of large and microcirculatory vessels, edematous fluid, and thrombi ( Figure 3) . A comparative intergroup analysis revealed that patients with disease duration of 10 days or more had significantly higher mean optical density of VWF staining in the endothelium of arteries, veins, arterioles, and venules (Table 2, Figure 4 ). Table 2 . Comparative intergroup analysis of mean optical density in pulmonary vascular endothelium in groups of patients with duration of disease more/less than 10 days.

Disease A comparative intergroup analysis revealed that patients with disease duration of 10 days or more had significantly higher mean optical density of VWF staining in the endothelium of arteries, veins, arterioles, and venules (Table 2, Figure 4 ). Patients with thrombotic complications (PE and/or thrombosis) had significantly higher mean optical density in the endothelium of veins and arteries compared to patients without thrombotic complications (Table 3) . Table 3 . Comparative intergroup analysis of mean optical density in pulmonary vascular endothelium in groups of patients with/without thrombotic complications.

Mean optical density in arteries 0. 45 Patients with thrombotic complications (PE and/or thrombosis) had significantly higher mean optical density in the endothelium of veins and arteries compared to patients without thrombotic complications (Table 3) . Patients with thrombosis had significantly higher mean optical density in the endothelium of arteries, veins, and arterioles than patients with PE (Table 4 ). 

Arteries. Increased mean optical density in arterial endothelium by multivariable analysis was associated with disease duration of more than 10 days, thrombotic complications, ventilatory support, and bacterial pneumonia (Table 5 ). Veins. Increased mean optical density in the venous endothelium was associated with disease duration of more than 10 days, thrombotic complications, and female sex ( Table 6 ). Arterioles. Increased mean optical density in the endothelium of arterioles was associated with a disease duration of more than 10 days, thrombotic complications, and bacterial pneumonia ( Table 7 ). Venules. Increased optical density in venule endothelium was associated with bacterial pneumonia and female sex (Table 8) . Table 8 . Multivariable regression analysis: independent predictors of increased optical density (above 0.49) in venule endothelium (with adjusted odds ratio calculation). 

Increased intensity of VWF immunostaining in pulmonary endothelium, a trend toward increasing rate of pulmonary arterial thrombosis in patients with disease duration of more than 10 days, supported the hypothesis regarding progression of circulatory disorders across the entire period of the disease. The important role of VWF in the pathogenesis Viruses 2022, 14, 211 9 of 13 of thrombosis in COVID-19 was proved by significantly higher intensity of IHC reaction in pulmonary vascular endothelium of patients with thrombosis compared to patients with PE. Several studies showed the association of high blood VWF levels with arterial thrombosis [24] . Kim et al., using simulation of arterial thrombosis in silico, in vitro, and in vivo, demonstrated an important role of VWF present in α-granules of platelets in the development of occlusive arterial thrombosis [25] . However, the results of published studies concerning the relationship between venous thrombosis and VWF are contradictory [26] .

The VWF is produced and secreted by endothelial cells, megakaryocytes, and platelets. The majority of VWF (80-90%) in blood plasma is produced by endothelial cells. The secretion of VWF from Weibel-Palade bodies occurs in response to endothelial-damaging factors of various etiologies. The VWF forms multimers (ultralarge von Willebrand factor, or ULvWF), the size of which is regulated by ADAMTS-13 (A disintegrin and metalloproteinase with thrombospondin-type motifs), sometimes called VWF-cleaving protease. The larger the size of the VWF multimer, the greater its functional activity. Thus, the cleavage or reduction in VWF multimers by the metalloproteinase ADAMTS-13 is essential for the maintenance of normal hemostasis. In the absence of ADAMTS-13 activity, as in patients with ADAMTS-13 mutations or acquired autoantibodies that block ADAMTS-13 activity, ULvWF "chords" with adhesive properties capture platelets and promotes thrombosis [27] .

The most severe deficiency (<10% of the reference values) of ADAMTS-13 occurs in thrombocytopenic purpura, a condition characterized by large VWF multimer sizes and, consequently, an increased risk of thrombosis. Since COVID-19 is associated with a significant increase in VWF levels, there is a relative deficiency of ADAMTS-13, resulting in large VWF multimers [28] . A number of studies have reported an imbalance of VWF and ADAMTS-13 in COVID-19 patients, which is associated with a high thrombotic risk [21, 29, 30] .

Philippe et al. showed that VWF was the best predictor of hospital mortality in COVID-19, and its serum levels correlated with the disease severity. A high level of highmolecular-weight VWF multimers in the blood of critically ill COVID-19 patients has been reported [31] .

Interestingly, bacterial pneumonia and ventilator support are among factors associated with the enhanced immunostaining for VWF in the pulmonary endothelium. The increase in VWF factor in plasma, in combination with reduced level of metalloproteinase responsible for its cleavage, were found not only in COVID-19, but also in community-acquired pneumonia [32] . The ability of the most common pneumonia pathogen Streptococcus pneumoniae to induce exocytosis of Weibel-Palade bodies and VWF and interleukin 8 (IL-8) release from pulmonary endothelial cells has been reported [33] .

Lung ventilation is an essential component of the comprehensive treatment of critically ill patients. At the same time, it can be associated with many complications [34] . Ventilatorinduced lung injury includes barotrauma, volutrauma, and biotrauma, among others. Plasma levels of interleukin 6, interleukin-8, surfactant protein D, and soluble tumor necrosis factor receptor I/II (sTNFrI/II), as well as endothelial damage markers such as intercellular adhesion molecule-1 (ICAM-1) and VWF, have been shown to be elevated in patients with acute lung injury, and their levels change rapidly in response to different ventilation strategies [35] . Ware et al. found that VWF is an independent predictor of hospital mortality in patients with acute lung injury and ARDS, and also showed an increase in VWF in plasma, depending on the duration of lung ventilation [36] . Yiming et al. examined the interaction of platelets with endothelial cells during experimental lung ventilation with high tidal volume. The authors found that during ventilation, platelets transported the platelet-binding proteins, including VWF, to the surface of endothelial cells [37] . Hegeman et al. showed that alveolar distension developing in ventilation induced pulmonary endothelial activation in healthy mice, which was characterized by higher expression of E-selectin and VCAM-1 mRNA [38] . Pulmonary artery thrombosis was detected in a morphological study of rat lungs, 24 h after a 2 h ventilation with a flow rate of 1 L/min [34] .

Thrombus formation in COVID-19 is not limited to the pulmonary vessels. This is confirmed by complications such as ischemic stroke [7] bowel ischemia [39] , liver sinusoidal thrombosis [40] , and disseminated intravascular coagulation [10] . Based on the results of studies confirming the increase in the VWF levels and the inhibition and/or decrease in the activity of ADAMTS-13 in COVID-19 [41] , it could be that the described changes in pulmonary vascular endothelium are systemic, and the VWF plays a key role in thrombus formation in all organs. In addition, an increase in the factor in the endothelium of other organs may be due to hypoxia, which develops as a result of respiratory failure [42] . At the same time, a number of factors affect the pulmonary vascular endothelium, the influence of which is absent in other organs: baro-and volutrauma during mechanical ventilation, or inflammation associated with bacterial infection. Studies of vascular endothelium in the other organs using similar methods can be useful for providing a rationale for the role of VWF in thrombotic events in other organs.

It can be assumed that the increased intensity of IHC staining for VWF in the pulmonary vessels was the result of its enhanced multimerization and platelet adhesion to these multimers. Several studies showed the increased number of pulmonary megakaryocytes in patients with acute lung injury and ARDS of various etiologies, including COVID-19 [43] [44] [45] . During histological examination, we noted the presence of single megakaryocytes in the lungs, but not in all cases. Samsonova M.V. et al. showed [46] single megakaryocytes in the capillaries of the interalveolar septa in the lungs of those who died from COVID-19 in the first week of the disease. Intensity of VWF immunohistochemical staining in the endothelium according to the results of our study is noted at later stages of the disease. Nevertheless, we cannot rule out the role of megakaryocytes in the pathogenesis of pulmonary vascular thrombosis. Additional studies are required to precisely define the contribution of megakaryocytes in thrombus formation in COVID-19.

The low percentage of thrombosis early in the disease is consistent with the hypothesis of gradual depletion of the protease ADAMTS-13 in COVID-19 and its deficiency late in the disease, which leads to an increase in the size and number of VWF multimers underlying thrombus formation. Since bacterial pneumonia and lung ventilation are independent predictors of increased IHC reaction for VWF, more focus should be placed on the role of lung ventilation and superinfection in the pathogenesis of thrombus formation in COVID-19.

A high incidence of thrombosis, shown by increased immunostaining intensity for VWF in pulmonary vascular endothelium of patients with a disease duration of more than 10 days, confirmed the hypothesis of circulatory disorder progression during the entire period of COVID-19. The important role of VWF in thrombosis development in COVID-19 was supported by significantly more intensive VWF immunostaining in pulmonary vessel endothelium of patients with thrombotic complications than the patients without thrombotic complications. At the same time, patients with thrombosis had significantly higher VWF immunostaining intensity in the arterial, venous, and arteriolar endothelium than those with pulmonary embolism. The disease duration and thrombotic complications were found to be independent predictors of the increased intensity of immunostaining for VWF in the endothelium of pulmonary arteries, veins, and arterioles. The results of the study demonstrated an important role of endothelial VWF in the pathogenesis of pulmonary vascular thrombosis in COVID-19. 

The data that support the findings of this study are available from the corresponding author upon reasonable request. Participant data without names and identifiers will be made available after approval from the corresponding author and local Ethics Committee.

The authors declare no conflict of interest.

Coronavirus Disease (COVID-19) Pandemic. Available online

The protein expression profile of ACE2 in human tissues

Evidence of SARS-CoV-2 Replication and Tropism in the Lungs, Airways and Vascular Endothelium of Patients with Fatal COVID-19: An Autopsy Case-Series

Thrombosis in COVID-19

Severe Neurologic Complications of SARS-CoV-2

Cardio-Pulmonary-Renal Consequences of Severe COVID-19

Brain Morphological Changes in COVID-19

SARS-CoV-2 Viremia is Associated with COVID-19 Severity and Predicts Clinical Outcomes

SARS-CoV-2 viremia is associated with distinct proteomic pathways and predicts COVID-19 outcomes

Incidence of thrombotic complications in critically ill ICU patients with COVID-19

Thromboelastometry in Neonates with Respiratory Distress Syndrome: A Pilot Study. Diagnostics 2021

Diagnosis, prevention, and treatment of thromboembolic complications in COVID-19: Report of the national institute for public health of the Netherlands

Coagulation disorders in coronavirus infected patients: COVID-19, SARS-CoV-1, MERS-CoV and lessons from the past

Features of pathological anatomy of lungs at COVID-19. Pulmonologiya 2020

COVID-19 is, in the end, an endothelial disease

Markers of endothelial and epithelial pulmonary injury in mechanically ventilated COVID-19 ICU patients

Distinct temporal characteristics of circulating alveolar epithelial and endothelial injury markers in ARDS with COVID-19

Time to consider histologic pattern of lung injury to treat critically ill patients with COVID-19 infection

The vascular endothelium: The cornerstone of organ dysfunction in severe SARS-CoV-2 infection

COVID-19 Vasculopathy: Mounting Evidence for an Indirect Mechanism of Endothelial Injury

Letter in response to: Circulating von Willebrand factor and high molecular weight multimers as markers of endothelial injury predict COVID-19 in-hospital mortality

Significance of von Willebrand factor in septic and nonseptic patients with acute lung injury

Prevention, Diagnosis and Treatment of New Coronavirus Infection (COVID-19)

_COVID-19_%28v.9%29.pdf

Role of von Willebrand factor for the onset of arterial thrombosis

Platelet α-granules are required for occlusive high-shear-rate thrombosis

Von Willebrand factor and thrombosis

ADAMTS13 and von Willebrand factor in thrombotic thrombocytopenic purpura

Willebrand Factor Multimer Formation Contributes to Immunothrombosis in Coronavirus Disease

Release of endothelial activation markers in lungs of patients with malaria-associated acute respiratory distress syndrome

Increased VWF and Decreased ADAMTS-13 in COVID-19: Creating a Milieu for (Micro)Thrombosis

Circulating Von Willebrand factor and high molecular weight multimers as markers of endothelial injury predict COVID-19 in-hospital mortality

Pro-coagulant imbalance in patients with community acquired pneumonia assessed on admission and one month after hospital discharge

Streptococcus pneumoniae induces exocytosis of Weibel-Palade bodies in pulmonary endothelial cells

Artificial Ventilation-Induced Acute Lung Lesion: Experimental, Morphological Study

Biological markers of lung injury before and after the institution of positive pressure ventilation in patients with acute lung injury

Willebrand factor antigen is an independent marker of poor outcome in patients with early acute lung injury

Platelets enhance endothelial adhesiveness in high tidal volume ventilation

Ventilatorinduced endothelial activation and inflammation in the lung and distal organs

Bowel Ischemia in COVID-19 Infection: One-Year Surgical Experience

Pathological characteristics of liver sinusoidal thrombosis in COVID-19 patients: A series of 43 cases

Coagulopathy and Thrombosis as a Result of Severe COVID-19 Infection: A Microvascular Focus

Hypoxia results in upregulation and de novo activation of von Willebrand factor expression in lung endothelial cells

Increased number of pulmonary megakaryocytes in COVID-19 patients with diffuse alveolar damage: An autopsy study with clinical correlation and review of the literature

Megakaryocytes and platelet homeostasis in diffuse alveolar damage

Amicus or Adversary Revisited: Platelets in Acute Lung Injury and Acute Respiratory Distress Syndrome

Lung pathology of COVID-19 in Moscow