Novel coronavirus pneumonia (NCP) and acute respiratory distress syndrome (ARDS) are both associated with the prevailing upper respiratory tract infections caused by the RNA-containing SARS-CoV2 virus of the genius Betacoronavirus of the Coronaviridae family. As both the viral infiltration and infection progress, the host immune system response can be one of a rapidly developing fatal cytokine storm. In the ARDS or NCP ensuing progression, the patient often succumbs to the effects of the hyper pro-inflammatory response, hence contributing to the associated increased mortality as a result of the cytokine storm and associated pathogenesis.

In December of 2019, in Wuhan, China, a novel coronavirus outbreak began. Globally this disease referred to as COVID-19, is the result of a novel SARS-CoV2 virus which predominantly targets Type II lung alveolar cells (AT2). The hyper response of the host immune system can rapidly evolve into a life-threatening cytokine-release syndrome or cytokine storm. The cytokine storm can predispose the patient to ARDS and/or NCP., or both. Left unchecked, the ARDS pathogenesis rapidly culminates in disruption of cell cytotoxicity mechanisms, excessive activation of cytotoxic lymphocytes, and a predominance of type I (M1) macrophage; resulting in the massive release of a host of proinflammatory cytokines (FNO-α, IL-1, IL-2, IL-6, IL-8, IL-10), granulocytic colony-stimulating factor, monocytic chemoattractive protein 1. The result systemically is a rise in surrogate inflammatory markers (C Reactive Protein, serum ferritin), with a corresponding infiltration of internal organs and tissues by activated macrophage, T-lymphocytes and a predominance of cellular apoptosis. The resulting hyperinflammatory pathogenic reaction may result in severe aveolar lesions leading to death, scarring, or severe lung damage, persisting well after discharge.

Experimental studies have demonstrated that mesenchymal stem cells (MSCs) and MSC-culutre media (MSC-CM) may significantly reduce the pro-inflammatory bias and associated pathologic impairment resulting. The MSC-CM, known to contain exosomes, has been shown to have an anti-inflammatory effect. Further exosomes associated with the amniotic membrane, long used in the treatment of burn and wounds, have been show to have a regenerative effect.

The purpose of this protocol is to explore the safety and efficacy of an intravenous injection of MSC derived exosomes in the treatment of severe patients (moderate to severe Berlin score) with ARDS or NCP.

Inclusion Criteria:

• Informed Consent given

• Male and female patients age 18 years or older

• Patients with coronavirus (SARS-CoV-2) infection confirmed prior to enrollment by any test with local regulatory approval

• Patients who require intensive care as determined by the following objective criteria:

  • Respiratory rate>25/minute
  • Oxygen saturation <93% on room air; or the
  • Use of high flow oxygen by nasal cannula at a rate ≥ 4L/minute.

• Patients with lung imaging demonstrating bilateral or diffuse pulmonary infiltrates on chest X-ray or CT scan.

• Patients with moderate to severe ARDS as defined by Berlin Criteria

• Patients who require invasive mechanical ventilation (IMV)

Exclusion Criteria:

• Patients will be excluded from the study if ONE of the following applies:

  • History of hypersensitivity to any drugs of similar classes to exosomes
  • Suspected active uncontrolled bacterial, fungal, or viral (besides SARS-CoV-2) infection
  • Currently receiving ECMO, nitric oxide therapy, or high-frequency oscillatory ventilation
  • In the option of the investigator, the patient is unlikely to survive for more than 24 hours post-enrollment
  • Patients who are on long-term use of select oral or injectable anti-rejection or immunomodulatory drugs
  • Pregnant or nursing (lacking) women

Open-label for the first 15 patients treated in dose escalation.

The final 40 participants are included in RCT. Double; participant and physician are masked.