Recommendation: Treatment of clinical long COVID encephalopathies with nasal administered mesenchymal stromal cell extracellular vesicles

IF 4.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
P. Askenase
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引用次数: 2

Abstract

We propose therapy with extracellular vesicles (EVs) for dominant central nervous system aspects of chronic Long COVID Syndromes (LCS). These clinical conditions have a delayed onset of 1–3 months following the cessation of active SARS-CoV-2 virus infections that cause an acute disease called COVID-19. The therapy of LCS will be achieved by direct access to the central nervous system (CNS) by nasal administration of small EVs derived from Mesenchymal Stromal Cells (MSC). When administered nasally, they target CNS microglia and endothelia involved in LCS encephalopathy, as indicated by experimental animal models and human autopsy and spinal fluid studies. Underlying this approach is the discovery that MSC-sEV treatment for healing neuro injury targets, microglia, and macrophages that then likely release secondary trophic EVs that affect the local capillary endothelial cells to restore vascular integrity. It is postulated that the pathways of endothelial and neural pathologies in acute SARS-CoV-2 virus infections may carry over to produce underlying vascular and neurological defects mediating LCS that are susceptible to this proposed nasal therapy with MSC-sEVs.
建议:经鼻给药间充质间质细胞胞外囊泡治疗临床长冠脑病
我们提出用细胞外小泡(EVs)治疗慢性Long COVID综合征(LCS)的主要中枢神经系统方面。在导致一种称为新冠肺炎的急性疾病的活动性SARS-CoV-2病毒感染停止后,这些临床疾病的发病延迟1-3个月。LCS的治疗将通过鼻腔给药来源于间充质基质细胞(MSC)的小EVs直接进入中枢神经系统(CNS)来实现。如实验动物模型、人体尸检和脊髓液研究所示,经鼻给药时,它们靶向参与LCS脑病的中枢神经系统小胶质细胞和内皮细胞。这种方法的基础是发现MSC sEV治疗神经损伤的靶点、小胶质细胞和巨噬细胞,然后可能释放影响局部毛细血管内皮细胞以恢复血管完整性的次级营养EV。据推测,急性严重急性呼吸系统综合征冠状病毒2型病毒感染中的内皮和神经病理通路可能会继续产生介导LCS的潜在血管和神经缺陷,这些缺陷易受MSC sEV鼻治疗的影响。
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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来源期刊
Frontiers in Nanotechnology
Frontiers in Nanotechnology Engineering-Electrical and Electronic Engineering
CiteScore
7.10
自引率
0.00%
发文量
96
审稿时长
13 weeks
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