47D11 抗体工程外泌体用于COVID-19患者雷米地韦的靶向给药:梦想还是原则?(评论性研究)。

Pub Date : 2022-10-01 DOI:10.5152/eurasianjmed.2022.21116
Nahid Daneshi, Abdolreza Esmaeilzadeh, Nazila Bahmaie
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引用次数: 0

摘要

近几个月来,随着冠状病毒2019年最新注册送彩金感染的高传播率,冠状病毒2019年最新注册送彩金在危重病人,尤其是老年人或免疫缺陷患者中的发病率和死亡率也有所上升。因此,迫切需要通过基于免疫病理生理学和免疫疗法的策略为这些患者开发更有效的治疗药物。在此,我们假设将表达S1b-RBD的间充质干细胞衍生外泌体(之前已用雷米替韦富集)与47D11抗体混合,可望保证这些靶向外泌体有效转移到2019年冠状病毒疾病感染的靶向微环境中。此外,它还能诱导其免疫调节特性和抗病毒功能,阻止严重急性呼吸系统综合征相关冠状病毒-2进入血管紧张素转换酶2表达细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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47D11 Antibody-Engineered Exosomes for Targeted Delivery of Remdesivir in Patients with COVID-19: Dream or Principle? (A Critical Editorial Study).

Along with the high transmission rate of coronavirus disease 2019 infection in the last few months, the morbidity and mortality rate of coronavirus disease 2019 has been increased among critically-ill patients, especially the elderly or the ones with immunodeficiencies. So, there is an urgent need to develop more effective therapeutic agents through immunopathophysiological and immunotherapeutic-based strategies for these patients. Here, we hypothesize that mixing S1b-RBD-expressing mesenchymal stem cell-derived exosomes (which have been previously enriched with Remdesivir) with 47D11 antibody, can promisingly guarantee effective transferring of those targeted exosomes to the targeted microenvironment of coronavirus disease 2019 infection. In addition, it can induce their immunomodulatory properties, and anti-viral features, refraining from entrance of severe acute respiratory syndrome-related coronavirus-2 to angiotensin-converting enzyme 2-expressing cells.

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