Randomized double-blind clinical study in patients with COVID-to evaluate the safety and efficacy of a phytomedicine (P Et)
Ahmed Mostafa, Rasha E Shalaby, Susana Fiorentino, Ballesteros -Ramírez, R Gomez-Cadena, Barreto, Claudia Urueña, Ricardo Ballesteros-Ramírez, Alejandra Gomez-Cadena, Alfonso Barreto, Karol Prieto, Sandra Quijano, Pablo Aschner, Carlos Martínez, Maria I Zapata-Cardona, Hajar El-Ahanidi, Camilla Jandus, Lizdany Florez-Alvarez, Maria Teresa Rugeles, Wildeman Zapata-Builes, Angel Alberto Garcia
Background: It has been proposed that polyphenols can be used in the development of new therapies against COVID-, given their ability to interfere with the adsorption and entrance processes of the virus, thus disrupting viral replication. Seeds from Caesalpinia spinosa, have been traditionally used for the treatment of inflammatory pathologies and respiratory diseases. Our team has obtained an extract called P Et, rich in polyphenols derived from gallic acid with significant antioxidant activity, and the ability to induce complete autophagy in tumor cells and reduce the systemic inflammatory response in animal models. Methods: In this work, a phase II multicenter randomized double-blind clinical trial on COVID-patients was designed to evaluate the impact of the P Et treatment on the clinical outcome and the immunological parameters related to the evolution of the disease. The Trial was registered with the number No. NCT * . A complementary study in an animal model of lung fibrosis was carried out to evaluate in situ lung changes after P Et in vivo administration. The ability of P Et to inhibit the viral load of murine and human coronaviruses in cellular models was also evaluated. Results: Patients treated with P Et were discharged on average after . days of admission vs. . days in the placebo group. Although a decrease in proinflammatory cytokines such as G-CSF, IL-, IL-, IL-, IP , MCP-, Frontiers in Medicine frontiersin.org Urueña et al. . /fmed. . MCP-and IL-was observed in both groups, P Et decreased to a greater extent G-CSF, IL-and IL-among others, which are related to lower recovery of patients in the long term. The frequency of T lymphocytes (LT) CD +, LT double negative (CD +CD -CD -), NK cells increased in the P Et group where the population of eosinophils was also significantly reduced. In the murine bleomycin model, P Et also reduced lung inflammation and fibrosis. P Et was able to reduce the viral replication of murine and human coronaviruses in vitro, showing its dual antiviral and anti-inflammatory role, key in disease control. Conclusions: Taken together these results suggest that P Et could be consider as a good co-adjuvant in the treatment of COVID-.
Ethics statement The studies involving human participants were reviewed and approved by the independent Ethics Committees (IECs) of the Hospital Universitario San Ignacio (Approval: 2020/050) and Centro Cardiovascular Colombiano Clínica Santa María (Approval: 2021/177). Trial was registered with the number No. NCT04410510 ( https://clinicaltrials.gov/ct2/ show/NCT04410510 ). The patients/participants provided their written informed consent to participate in this study. The animal study was reviewed and approved by Veterinary Authority of the Swiss Canton Genève (authorization no. GE119/20).
Author contributions CU, RB-R, AB, and SF were responsible for the study design, interpretation of results, drafting and revising the manuscript. AG, CM, and PA participated in the recruitment of the COVID19 patients, acquisition, and analysis of clinical safety and efficacy data. KP, MZ-C, LF-A, WZ-B, and MR were responsible for the design, acquisition, and analysis of the in vitro COVID19 model. AG-C, HE-A, and CJ were responsible of the design, acquisition, and analysis of the in vivo lung model. All authors participated in drafting and revising the manuscript and have read and approved the final manuscript.
Conflict of interest Authors SF and CU are inventors of a granted patent related to P2Et. Authors SF, CU, and RB-R are partners of the DreemBio company who was a licensee of related patents. The remaining authors declare that the research was conducted in the absence of any..
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"abstract": "<jats:sec><jats:title>Background</jats:title><jats:p>It has been proposed that polyphenols can be used in the development of new therapies against COVID-19, given their ability to interfere with the adsorption and entrance processes of the virus, thus disrupting viral replication. Seeds from <jats:italic>Caesalpinia spinosa</jats:italic>, have been traditionally used for the treatment of inflammatory pathologies and respiratory diseases. Our team has obtained an extract called P2Et, rich in polyphenols derived from gallic acid with significant antioxidant activity, and the ability to induce complete autophagy in tumor cells and reduce the systemic inflammatory response in animal models.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>In this work, a phase II multicenter randomized double-blind clinical trial on COVID-19 patients was designed to evaluate the impact of the P2Et treatment on the clinical outcome and the immunological parameters related to the evolution of the disease. The Trial was registered with the number No. NCT04410510<jats:sup>*</jats:sup>. A complementary study in an animal model of lung fibrosis was carried out to evaluate <jats:italic>in situ</jats:italic> lung changes after P2Et <jats:italic>in vivo</jats:italic> administration. The ability of P2Et to inhibit the viral load of murine and human coronaviruses in cellular models was also evaluated.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Patients treated with P2Et were discharged on average after 7.4 days of admission vs. 9.6 days in the placebo group. Although a decrease in proinflammatory cytokines such as G-CSF, IL-15, IL-12, IL-6, IP10, MCP-1, MCP-2 and IL-18 was observed in both groups, P2Et decreased to a greater extent G-CSF, IL-6 and IL-18 among others, which are related to lower recovery of patients in the long term. The frequency of T lymphocytes (LT) CD3+, LT double negative (CD3+CD4-CD8-), NK cells increased in the P2Et group where the population of eosinophils was also significantly reduced. In the murine bleomycin model, P2Et also reduced lung inflammation and fibrosis. P2Et was able to reduce the viral replication of murine and human coronaviruses <jats:italic>in vitro</jats:italic>, showing its dual antiviral and anti-inflammatory role, key in disease control.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Taken together these results suggest that P2Et could be consider as a good co-adjuvant in the treatment of COVID-19.</jats:p></jats:sec><jats:sec><jats:title>Clinical trail registration</jats:title><jats:p><jats:ext-link>https://clinicaltrials.gov/ct2/show/NCT04410510</jats:ext-link>, identifier: NCT04410510.</jats:p></jats:sec>",
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