一种治疗SARS-CoV-2病毒诱导的病原抗体和疫苗引起的不良反应的候选药物

Huiru Wang, Xiancong Wu, L. Dai, Yue Hu, Yuekai Zhang, Yuxing Chen, Xiaoling Liu
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引用次数: 0

摘要

在最近的一项研究中,我们报道了SARS-CoV-2和SARS-CoV病毒的某些抗刺突抗体可以通过与患病的肺上皮细胞结合并误导免疫反应来攻击自身细胞而产生致病作用。我们将这种新的致病机制称为“抗体依赖性自动攻击”(ADAA)。本研究探索了一种预防和治疗此类adaa型疾病的候选药物。该候选药物是一种含有n -乙酰神经氨酸甲酯(na - me)的制剂,n -乙酰神经氨酸的类似物。na - me通过一种独特的作用机制(MOA)起作用,即修复患病肺上皮细胞缺失的唾液酸。该MOA可以阻断抗体与易受病原感染的病细胞的结合,预防和治疗新冠肺炎疫苗的不良反应,因为疫苗可以诱导类似的抗体,包括病原抗体。该配方将有助于在不降低疫苗效力的情况下提高疫苗的安全性。与现有抗病毒药物相比,该制剂具有独特的靶向受体MOA,适应症广泛,安全性好,耐突变,易于生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Drug Candidate for Treating Adverse Reactions Caused by Pathogenic Antibodies Inducible by SARS-CoV-2 Virus and Vaccines
In a recent study, we reported that certain anti-spike antibodies of SARS-CoV-2 and SARS-CoV viruses can have a pathogenic effect through binding to sick lung epithelium cells and misleading immune responses to attack self-cells. We termed this new pathogenic mechanism “Antibody Dependent Auto-Attack” (ADAA). This study explores a drug candidate for prevention and treatment of such ADAA-based diseases. The drug candidate is a formulation comprising N-acetylneuraminic acid methyl ester (NANA-Me), an analog of N-acetylneuraminic acid. NANA-Me acts through a unique mechanism of action (MOA) which is repairment of the missing sialic acid on sick lung epithelium cells. This MOA can block the antibodies’ binding to sick cells, which are vulnerable to pathogenic to prevent and treat the adverse reactions of COVID-19 vaccines because the vaccines can induce similar antibodies, including pathogenic antibodies. The formulation will be helpful in increasing the safety of the vaccines without reducing the vaccine’s efficacy. Compared to existing antiviral drugs, the formulation has a unique MOA of targeting receptors, broad spectrum of indications, excellent safety profile, resistance to mutations, and can be easily produced.
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