Urueña Claudia, Ballesteros-Ramírez Ricardo, Gomez-Cadena Alejandra, Barreto Alfonso, Prieto Karol, Quijano Sandra, Aschner Pablo, Martínez Carlos, Zapata-Cardona Maria I, El-Ahanidi Hajar, Jandus Camilla, Florez-Alvarez Lizdany, Rugeles Maria Teresa, Zapata-Builes Wildeman, Garcia Angel Alberto, Fiorentino Susana
Grupo de Inmunobiologiay Biología Celular, Facultad de Ciencias, Unidad de Investigación en Ciencias Biomédicas, Pontificia Universidad Javeriana, Bogotá, Colombia.
Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
Front Med (Lausanne). 2022 Sep 8;9:991873. doi: 10.3389/fmed.2022.991873. eCollection 2022.
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 , 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.
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. A complementary study in an animal model of lung fibrosis was carried out to evaluate lung changes after P2Et administration. The ability of P2Et to inhibit the viral load of murine and human coronaviruses in cellular models was also evaluated.
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 , showing its dual antiviral and anti-inflammatory role, key in disease control.
Taken together these results suggest that P2Et could be consider as a good co-adjuvant in the treatment of COVID-19.
https://clinicaltrials.gov/ct2/show/NCT04410510, identifier: NCT04410510.
鉴于多酚能够干扰病毒的吸附和进入过程,从而破坏病毒复制,有人提出多酚可用于开发抗新冠病毒的新疗法。[植物名称]的种子传统上用于治疗炎症性疾病和呼吸道疾病。我们的团队获得了一种名为P2Et的提取物,其富含源自没食子酸的具有显著抗氧化活性的多酚,并且能够在肿瘤细胞中诱导完全自噬,并在动物模型中降低全身炎症反应。
在这项研究中,设计了一项针对新冠患者的II期多中心随机双盲临床试验,以评估P2Et治疗对临床结局以及与疾病进展相关的免疫参数的影响。该试验已在ClinicalTrials.gov上注册,注册号为NCT04410510。在肺纤维化动物模型中进行了一项补充研究,以评估给予P2Et后的肺部变化。还评估了P2Et在细胞模型中抑制鼠冠状病毒和人冠状病毒病毒载量的能力。
接受P2Et治疗的患者平均入院7.4天后出院,而安慰剂组为9.6天。尽管两组中促炎细胞因子如粒细胞集落刺激因子(G-CSF)、白细胞介素-15(IL-15)、白细胞介素-12(IL-12)、白细胞介素-6(IL-6)、干扰素诱导蛋白10(IP10)、单核细胞趋化蛋白-1(MCP-1)、单核细胞趋化蛋白-2(MCP-2)和白细胞介素-18均有所下降,但P2Et组中G-CSF、IL-6和IL-18等下降幅度更大,而这些细胞因子与患者长期恢复较差有关。P2Et组中T淋巴细胞(LT)CD3+、LT双阴性(CD3+CD4-CD8-)、自然杀伤细胞(NK细胞)的频率增加,嗜酸性粒细胞数量也显著减少。在鼠博来霉素模型中,P2Et还减轻了肺部炎症和纤维化。P2Et能够降低鼠冠状病毒和人冠状病毒的病毒复制,显示出其双重抗病毒和抗炎作用,这对疾病控制至关重要。
综合这些结果表明,P2Et可被视为治疗新冠的良好辅助药物。
https://clinicaltrials.gov/ct2/show/NCT04410510,标识符:NCT04410510。