Daneshi Nahid, Esmaeilzadeh Abdolreza, Bahmaie Nazila
Zanjan University of Medical Sciences (ZUMS) Faculty of Medicine, Zanjan, Iran.
Department of Immunology, Zanjan University of Medical Sciences (ZUMS) Faculty of Medicine, Zanjan,Iran; Immunotherapy Research - Technology Group, Zanjan University of Medical Sciences, Zanjan (ZUMS), Iran.
Eurasian J Med. 2022 Oct;54(3):310-312. doi: 10.5152/eurasianjmed.2022.21116.
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.
在过去几个月里,随着2019冠状病毒病感染的高传播率,2019冠状病毒病在重症患者中的发病率和死亡率有所上升,尤其是老年人或免疫功能低下者。因此,迫切需要通过基于免疫病理生理学和免疫治疗的策略,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(此前已富集瑞德西韦)与47D11抗体混合,有望保证这些靶向外泌体有效地转移到2019冠状病毒病感染的靶向微环境中。此外,它可以诱导其免疫调节特性和抗病毒特性,防止严重急性呼吸综合征相关冠状病毒-2进入表达血管紧张素转换酶2的细胞。