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口服 IMM-124E 增强抗病毒 T 细胞免疫应答:预防和治疗 COVID-19 的一种方法在临床前模型和 I/IIa 期临床试验中的研究。

Augmented antiviral T cell immunity by oral administration of IMM-124E in preclinical models and a phase I/IIa clinical trial: A method for the prevention and treatment of COVID-19.

机构信息

Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel.

出版信息

Drug Dev Res. 2022 May;83(3):615-621. doi: 10.1002/ddr.21890. Epub 2021 Oct 1.

Abstract

Biological adjuvants that target the gut immune system are being developed for modulating the immune system. Hyperimmune bovine colostrum (HBC), produced by harvesting the bovine colostrum of dairy cows immunized to exogenous antigens, has been shown to modulate the immune responses and alleviate immune-mediated organ damages. The aim of the present study was to determine the ability of HBC to promote antiviral interferonγ (IFNγ) T cell responses. In a preclinical study, mice were orally administered with HBC for 5 days and tested for the number of T cell clones secreting IFNγ in response to viral antigens of the swine flu, New Caledonia influenza, and cytomegalovirus. In a phase I/IIa clinical trial, five healthy volunteers were treated for 5 days with HBC followed by testing the anti-coronavirus disease (COVID-19) immunity. In the preclinical study, oral administration of HBC augmented the number of T cell clones secreting IFNγ in response to viral antigens. In the clinical trial, oral administration of HBC to healthy males significantly increased the number of anti-COVID-19 spike protein IFNγ positive T cell clones. Oral administration of HBC provides a novel method for augmenting antiviral responses. Its high-safety profile makes it ideal for all disease stages and for pre-emptive therapy among medical personnel and other workers who are at a high risk of exposure to infections. The relatively low cost of HBC is expected to minimize care provider burdens, costs, and enable its global application.

摘要

正在开发靶向肠道免疫系统的生物佐剂来调节免疫系统。从免疫外源抗原的奶牛采集的高免牛初乳(HBC)已被证明可调节免疫反应并减轻免疫介导的器官损伤。本研究的目的是确定 HBC 促进抗病毒干扰素γ(IFNγ)T 细胞反应的能力。在一项临床前研究中,用 HBC 对小鼠进行口服给药 5 天,并测试针对猪流感、新喀里多尼亚流感和巨细胞病毒的病毒抗原分泌 IFNγ的 T 细胞克隆的数量。在 I/IIa 期临床试验中,五名健康志愿者接受 HBC 治疗 5 天,然后测试对冠状病毒病(COVID-19)的免疫力。在临床前研究中,口服给予 HBC 可增加针对病毒抗原分泌 IFNγ的 T 细胞克隆的数量。在临床试验中,口服给予 HBC 可显著增加 COVID-19 刺突蛋白 IFNγ阳性 T 细胞克隆的数量。口服给予 HBC 提供了一种增强抗病毒反应的新方法。其高安全性使其成为所有疾病阶段的理想选择,并且适用于处于感染高风险的医务人员和其他工人的预防性治疗。HBC 的相对低成本有望减轻护理人员的负担、成本,并使其能够在全球范围内应用。

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