To access host cells, SARS-CoV-2 uses a surface glycoprotein (peplomer) known as spike; ACE2 has been shown to be a co-receptor for coronavirus entry ^[1]. Therefore, the density of ACE2 in each tissue may correlate with the severity of the disease in that tissue. Other factors on the surface of human cells have been suggested to mediate the entry of SARS-CoV-2, including transmembrane serine protease 2 (TMPRSS2), sialic acid receptors, and extracellular matrix metalloproteinase inducer (CD147, also known as basigin). Additionally, cathepsin B and L have been shown to be critical entry factors in the pathogenesis of COVID-19.

Intriguingly, all of these factors involved in the entry of SARS-CoV-2 in the host cell have been shown ^[2] to be expressed by endothelial cells (Figure 1).

ACE2 is the most studied of these receptors: its genetic inactivation has been demonstrated to cause severe lung injury in H5N1-challenged mice, whereas administration of recombinant human ACE2 ameliorates H5N1 virus-induced lung injury in mice ^[3].

Figure 1. Endothelial dysfunction is a major determinant of COVID-19.

The SARS-CoV-2 coronavirus accesses host cells via the binding of its spike glycoprotein to angiotensin-converting enzyme 2 (ACE2), sialic acid receptor, transmembrane serine protease 2 (TMPRSS2), and extracellular matrix metalloproteinase inducer (CD147); cathepsin B and L also participate in virus entry. All of these factors are expressed in endothelial cells. Endothelial dysfunction is a common feature of the clinical manifestations commonly observed in COVID-19 patients. All of the drugs proposed as a potential therapeutic strategy to treat COVID-19 patients have been shown to improve endothelial function, including tocilizumab, colchicine, chloroquine/hydroxychloroquine, and azithromycin, and famotidine (see text for details and references).

ACE2 is currently at the center of a heated debate among physicians, and there are concerns that medical management of hypertension, including the use of inhibitors of the renin-angiotensin-aldosterone system (RAAS), may contribute to the adverse health outcomes observed ^[4]. TMPRSS2 binds the viral spike glycoprotein ^[5]; recent structural assays have suggested that coronaviruses can bind sialic acid receptors; CD147 has been shown to be essential for the entry of cytomegalovirus into endothelial cells; both cathepsin B and L are present in endothelial cells (Figure 1) ^[6].

The endothelium prevents blood clotting by providing an antithrombotic surface, maintained by heparan sulphate present in the matrix surrounding the cells, by the expression of tissue factor inhibitor, thrombomodulin, and by the production of tissue-type plasminogen activator that promotes fibrinolysis ^[7].

Endothelial dysfunction refers to a systemic condition in which the endothelium loses its physiological properties, including the tendency to promote vasodilation, fibrinolysis, and anti-aggregation ^[8]; moreover, endothelial dysfunction appears to be a consistent finding in patients with diabetes ^[9].

The cases of Kawasaki disease and pediatric multisystem inflammatory syndrome (PMIS) reported in young COVID-19 patients support our view of a systemic vasculitis caused by SARS-CoV-2 ^[10].

COVID-19 patients often exhibit clotting disorders, with organ dysfunction and coagulopathy, resulting in higher mortality ^[11]. Critical data came from the analysis of coagulation tests including prothrombin time (PT), activated partial thromboplastin time (APTT), antithrombin activity (AT), fibrinogen, fibrin degradation product (FDP), and D-dimer, in samples collected on admission and during the hospital stay of COVID-19 patients. Non-survivors had significantly higher D-dimer and FDP levels, and longer PT vs survivors on admission ^[12]. Moreover, significant reduction and lowering of fibrinogen and AT levels were observed in non-survivors during late stages of hospitalization, which is compatible with a clinical diagnosis of disseminated intravascular coagulation (DIC). Specifically, among 191 COVID-19 patients seen at two hospitals in Wuhan, D-dimer levels over 1 μg/L at admission predicted an 18-fold increase in odds of dying before discharge ^[13]. When DIC is caused by a systemic infection, it features an acute systemic over-inflammatory response, strictly linked to endothelial dysfunction ^[14]. Most recently a case of a COVID-19 patient with an increase of Factor VIII clotting activity and a massive elevation of von Willebrand Factor (vWF) has been reported ^[15], further supporting our theory: indeed, vWF can be seen as a marker of endothelial damage, since it is normally stored in Weibel-Palade bodies within endothelial cells. Equally important, angiotensin II levels in the plasma of COVID-19 patients were markedly elevated and linearly associated to viral load and lung injury ^[16].

This entry is adapted from the peer-reviewed paper 10.3390/jcm9051417