Adoptive Cell Transfer for the Immunotherapy of COVID-19 in Colombia
Study Details
Study Description
Brief Summary
Immunotherapy based on Adoptive Cellular Transfer (ACT) uses several types of immune cells, including dendritic cells, cytotoxic T lymphocytes, lymphokine-activated killer cells, and NK cells. NK cell-based immunotherapies are an attractive approach for treating diseases because of their characteristic recognition and killing mechanisms; they are involved in the early defense against infectious pathogens and against MHC class-I-negative or -low-expressing targets without the requirement for prior immune sensitization of the host and are able to lyse target through the release of perforin and granzymes and using antibody-dependent cellular cytotoxicity pathways mediated by Fc receptor for IgG (CD16).
The aim of this project is to evaluate the safety and immunogenicity of allogeneic NK cells from peripheral blood mononuclear cells (PBMCs) of healthy donors in patients infected with COVID-19 collected by apheresis. This allows us to collect cGMP PBMCs and immunomagnetic remove several types of undesirable cells including B, T and CD33+ cells with enrichment of NK cells that will be expanded in bioreactors with GMP culture media (AIM-V) supplemented with human AB serum and GMP grade IL-2, and IL-15. After quality control verification the final NK cell product will be resuspended in 300 mL saline solution for intravenous infusion. Initially, we will enroll in this study ten COVID-19 infected adult patients with moderate symptoms (NEWS 2 scale score>4). Consent forms will be signed by the patient before the therapy. Patients will be treated with three different infusions of NK cells 48 h apart with 1, 10, and 20 million cells/kg body weight. We will follow the patients for any adverse effect, clinical response and immune effects by flow cytometry including markers for NK cells expressing different markers (CD158b, NKG2A, and IFN-y). We anticipated that the release of IFN-y by exogenous NK cells could attract other immune cell populations to boost the immune response against COVID-19.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treatment group Adult patients with COVID-19 infection with NEWS 2 score >4 |
Biological: Allogeneic NK transfer
Three doses of allogeneic NK cell transfer
|
Outcome Measures
Primary Outcome Measures
- Adverse effects and Safety [3 months]
Adverse effects monitoring during and after vaccination
Secondary Outcome Measures
- NK transfer Immunogenicity [6 months]
Measure of NK response against SARS-Cov2 virus
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age ≥ 18 years at the time of the evaluation
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Able and willing to understand the study, follow all study procedures, and provide written informed consent.
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Initial diagnosis of COVID-19 disease as defined by a molecular diagnostic test approved by the National Institute of Health positive for SARS-CoV-2
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Clinical presentation of moderate or severe (identified at the time of admission to the room by the National Early Warning Score NEWS-2; moderate >4)
Exclusion Criteria:
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Patients who are hospitalized for inpatient treatment or are currently being evaluated for possible hospitalization at the time of informed consent initiation.
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Oxygen saturation in ambient air of <92%
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History of Chronic Obstructive Pulmonary Disease (COPD)
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Participation in a clinical trial with or use of any investigational agent within 30 days prior to detection, or treatment with interferons (IFN) or immunomodulators within 12 months prior to detection
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Pregnant or lactating female patients.
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Current or previous history of decompensated liver disease (Child-Pugh Class B or C) or hepatocellular carcinoma
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Co-infected with the human immunodeficiency virus (HIV) or the hepatitis C virus (HCV)
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Significant abnormal laboratory test results on screening.
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Significant concurrent diseases and other comorbidities that may require intervention during the study.
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Concurrent use of any of the following medications: Therapy with an immunomodulatory agent. Current use of heparin o Coumadin. Received blood products within 30 days prior to study randomization. Use of hematological growth factors within 30 days prior to the randomization of the study. Any recipe or herbal product that is not approved by the researcher. Long-term treatment (> 2 weeks) with agents that have a high risk of nephrotoxicity or hepatotoxicity unless approved by the medical monitor. Receiving systemic immunosuppressive therapy within 3 months prior to detection.
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Considered by researchers to be unfit to participate in this clinical trial
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Chronic heart failure with ejection fraction less than 30%.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Fundacion Salud De Los Andes | Bogotá | Bogotá Distrito Capital | Colombia | 111321 |
| 2 | Universidad Nacional de Colombia | Bogota | Cundinamarca | Colombia | 111321 |
Sponsors and Collaborators
- Universidad Nacional de Colombia
- Fundación Salud de los Andes
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- UNAL FSA COVID
- Estudio Clinico