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Antibody Response to Severe Acute Respiratory Syndrome- Corona Virus 2, Diagnostic and Therapeutic Implications.针对严重急性呼吸综合征冠状病毒2的抗体反应及其诊断和治疗意义
Hepatol Commun. 2020 Sep 12;4(12):1731-1743. doi: 10.1002/hep4.1600. eCollection 2020 Dec.
2
The assembly of glycosphingolipid determines their immunomodulatory effect: A novel method for structure-based design of immunotherapy.糖脂的组装决定了它们的免疫调节作用:一种基于结构的免疫疗法设计新方法。
Cell Immunol. 2020 Sep;355:104157. doi: 10.1016/j.cellimm.2020.104157. Epub 2020 Jul 3.
3
Targeting SARS-CoV-2 receptors as a means for reducing infectivity and improving antiviral and immune response: an algorithm-based method for overcoming resistance to antiviral agents.靶向 SARS-CoV-2 受体作为降低感染性和改善抗病毒及免疫反应的手段:一种克服抗病毒药物耐药性的基于算法的方法。
Emerg Microbes Infect. 2020 Dec;9(1):1397-1406. doi: 10.1080/22221751.2020.1776161.
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The COVID-19 Pandemic in the US: A Clinical Update.美国的新冠疫情:临床最新情况
JAMA. 2020 May 12;323(18):1767-1768. doi: 10.1001/jama.2020.5788.
5
The role of the sphingolipid pathway in liver fibrosis: an emerging new potential target for novel therapies.鞘脂代谢通路在肝纤维化中的作用:新型治疗药物的新兴潜在靶点。
Am J Physiol Cell Physiol. 2020 Jun 1;318(6):C1055-C1064. doi: 10.1152/ajpcell.00003.2020. Epub 2020 Mar 4.
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Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study.中国武汉严重 COVID-19 患者的临床病程和结局:一项单中心、回顾性、观察性研究。
Lancet Respir Med. 2020 May;8(5):475-481. doi: 10.1016/S2213-2600(20)30079-5. Epub 2020 Feb 24.
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β-Glycosphingolipids as Mediators of Both Inflammation and Immune Tolerance: A Manifestation of Randomness in Biological Systems.β-糖鞘脂作为炎症和免疫耐受的介质:生物系统随机性的表现。
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Immune rebalancing by oral immunotherapy: A novel method for getting the immune system back on track.口服免疫治疗的免疫再平衡:让免疫系统重回正轨的新方法。
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Comparison of antiviral resistance across acute and chronic viral infections.急性和慢性病毒感染的抗病毒耐药性比较。
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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.

DOI:10.1002/ddr.21890
PMID:34596893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8652907/
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。