Direct endothelial damage and vasculitis due to SARS‐CoV‐2 in small bowel submucosa of COVID‐19 patient with diarrhea

Abstract

SARS-CoV-2, responsible for COVID-19, is a new virus that can infect different cellular lines, including endothelia and epithelial cells of the gastrointestinal tract mucosa. At this level, the virus can cause different types of direct damage, even in paucisymptomatic, young patients. Virus can be detected directly by immunohistochemical techniques. Coronaviruses are a family of positive single-stranded RNA viruses known since 1960s1-3 that can infect mainly the respiratory system, the liver and the bowel in various animal species, including humans. Emerging infections, such as Middle-East Respiratory Syndrome (MERS) and Severe Acute Respiratory Syndrome (SARS), are caused by coronaviruses. The most recent pathogen in this family is SARS-CoV-2, responsible for COVID-19.4 SARS-CoV-2 can infect different cellular lines expressing angiotensin-converting enzyme 2 (ACE-2), including ciliated respiratory cells in nasal sinuses and bronchial tree, alveolar pneumocytes, kidney tubular cells, small bowel, and colon mucosa.5-8 Cellular entry of the virus depends on the binding of the Spike protein present on the virus capsid to ACE2 protein, and on the priming of the spike by the cellular serine protease TMPRSS2. The binding is crucial not only for virus internalization, but also for COVID-19 pathogenesis, as blockage and downregulation of the receptors result in impaired cardiovascular function that may lead to Acute Respiratory Distress Syndrome (ARDS), which is the main clinical manifestation of the disease.6-8 Along the development of COViD-19 pandemics, gastro-intestinal symptoms such as diarrhea and abdominal pain have been reported in SARS-CoV-2-positive patients and are now recognized as a part of COViD-19 clinical spectrum.8 SARS-CoV-2 was recently found within endothelial cells of various organs, including the small bowel and the central nervous system, with Transmission Electron Microscopy (TEM) techniques.9, 10 We describe the histopathological findings in a 40 years old SARS-CoV-2-positive woman, presenting with diarrhea and abdominal pain, who underwent endoscopic biopsy sampling of the large bowel, in which we searched for the virus with immunohistochemical reaction on formalin-fixe paraffin-embedded tissue with antibodies directed against the SARS-CoV-2 nucleocapsid. The woman, with mild respiratory symptoms including cough and fever (>37,5°C) was quarantined after positive SARS-CoV-2 nasal swab and was later referred to the emergency unit for diarrhea and abdominal pain with anemia (Hb 7,8 g/dL). Upon admission, lung CT-scan was consistent with mild interstitial pneumonia. To investigate the causes of fecal occult blood test positivity a colonoscopy was performed. The exam highlighted two small ulcerative lesions on the ileocecal valve in an otherwise normal colon mucosa. Both lesions were sampled and sent for histopathological examination. The patient was treated with a unit of concentrated red blood cells plus iron supplementation and was discharged after normalization of Hb levels. Biopsy samples consisted of mucosal and submucosal tissue, with extensive lymphoplasmacellular inflammatory infiltrate. Immunophenotyping showed a substantial share of T-lymphocytes (mainly CD3+/CD4+, with a lesser proportion of CD3+/CD8+) (Figure 1A,B), prominent multifocal vasculitis (Figure 1C,D), and bizarre modifications of the endothelium of small- and middle-sized vessels (Figure 1E,F), sometimes showing obliterating arteriolitis (Figure 1G,H). Interestingly, no fibrinic microthrombi were found in these vessels. The mucosa showed ischemic damage. Immunohistochemical stains with an antibody directed against the nucleocapsid protein of SARS-CoV-2 (Rabbit monoclonal anti-nucleocapsid protein; Sino Biological Inc, Chesterbrook, PA) revealed the presence of virus particles in the cytoplasm of the endothelial cells with hobnail and bizarre features (Figure 1H). The immunohistochemical reaction was completely negative in non-endothelial cells (Figure 1I) and in control samples. These modifications may represent a peculiar cytopathic effect of the virus in this cellular line. The clinical setting of the patient and the recent reports of endothelial cells infection by SARS-CoV-2 suggest that patients with COVID-19 may suffer GI tract damage due to hyperinflammatory response,5, 7 hypercoagulability state, and endothelial dysfunction. Our findings suggest that this later feature might be directly caused by endothelial cell infection, resulting in endothelial cytopathic modifications, vascular obliteration and, even if not observed in our case, thrombosis of small- and middle-sized vessels. Similar findings were already described with TEM techniques on endothelia of the small bowel9 and central nervous system.10 We found a similar distribution of the virus in cytoplasm, also arranging in small clusters of particles. In the case of central nervous system infection, a viral hematogenous route using inflammatory cells as Trojan horse was proposed but, since we cannot demonstrate directly the presence of the virus in lymphocytes,10 this possibility seems now less probable to us: the direct infection of blood-brain barrier vessels may represent a more likely gate for the virus. Hobnail modifications of the endothelial cells, with bizarre nuclear shapes, may be an important hallmark to identify direct cytopathic effect of SARS-CoV-2 in this cellular line. These modifications and the presence of the virus with immunohistochemistry can be recognized directly by the pathologist, saving time and money to confirm a potential suspect of COVID-19, where reverse-transcription polymerase chain reaction on a swab was not already performed. The authors declare that there are no conflict of interests.

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