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Coronavirus Disease 2019 (COVID-19) is spreading worldwide and has become a public health emergency of major international concern. Currently, no specific drugs or vaccines are available. For severe cases, it was found that aberrant pathogenic T cells and inflammatory monocytes are rapidly activated and then producing a large number of cytokines and inducing an inflammatory storm. Mesenchymal stem cells (MSCs) have been shown to possess a comprehensive powerful immunomodulatory function. This study aims to investigate the safety and efficacy of intravenous infusion of mesenchymal stem cells in severe patients with COVID-19.
Coronavirus-19 Disease (COVID-19), caused by the Sars-Cov-2 virus, which occurs as a growing pandemic in early 2020 and currently represents an emergency state worldwide. Several reports have shown that the first step in the pathogenesis of Sars-Cov-2 is the recognition of the angiotensin I converting enzyme (ACE2) receptor by the virus. This ACE2 receptor is widely distributed on the surface of human cells, especially as type II alveolar cells and capillary endothelium, however bone marrow, lymph nodes, thymus and spleen are known as immune cells, such as T and lymphocytes. B and macrophages, are negatives to ACE2. These results suggest that immunotherapy can be used to treat infected patients. However, an immunomodulatory capacity cannot be so strong, if just one or two major immunological factors used, as the virus can cause a "cytokine storm", such as IL-2, IL-6, IL-7, GSCF, IP10 , MCP1, MIP1A and TNFα, followed by edema, gas exchange dysfunction, acute respiratory distress syndrome, cardiac injury and secondary infection that can lead to death. Therefore, avoiding a "cytokine storm" may be the key to treating patients infected with Sars-Cov-2. Mesenchymal stem cells (MSCs), due to their potential for immunomodulatory activity, can have beneficial effects in preventing or attenuating the cytokine storm. Because MSCs have been widely used in cell therapy, from basic research to clinical trials. Safety and efficacy have been clearly documented in several clinical trials, especially in immune-mediated inflammatory diseases, such as graft versus host disease (GVHD). The objective of the study is to verify the safety and feasibility of using allogeneic bone marrow mesenchymal stem cells in patients with SARS-CoV-2.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention | Experimental | Intravenous 1*10E6 MSCs/kg body weight Mesenchymal Stromal Cells infusion |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Mesenchymal Stromal Cells infusion | Biological | Intravenous 1*10E6 MSCs/kg body weight Mesenchymal Stromal Cells infusion |
|
| Measure | Description | Time Frame |
|---|---|---|
| Overall survival | Assessment of Overall survival at 30 days post intervention | 60 days |
| Measure | Description | Time Frame |
|---|---|---|
| Changes on inflammatory C-reactive protein | To assess the anti-inflammatory effect of the proposed treatment with assessment of the levels of C-reactive protein (mg/dL) | 60 days |
| Hospital stay |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Lucia Silla, MD, PhD | Contact | 55 51 33598371 | lsilla@hcpa.edu.br | |
| Annelise Pezzi, PhD | Contact | annepezzi@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Lucia Silla, MD, PhD | Hospital de Clinicas de Porto Alegre | Principal Investigator |
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| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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days of the patients in hospital
| 60 days |
| Oxygenation index (PaO2/FiO2) | Evaluation of functional respiratory changes: PaO2 / FiO2 ratio | 60 days |
| Improvement in Liao's score (2020) | Improvement in Liao's score (2020) | 60 days |
| Radiological improvement | Computed tomography Chest assesment will be done to assess improvement in radiological findings of COVID-19 | 60 days |
| Time of COVID19 PCR negativity | PCR testing to check PCR negativity | 28 days |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |