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10.3389/fimmu.2022.824378

http://scihub22266oqcxt.onion/10.3389/fimmu.2022.824378
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suck abstract from ncbi


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pmid35401544      Front+Immunol 2022 ; 13 (ä): 824378
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  • Preclinical Studies on Convalescent Human Immune Plasma-Derived Exosome: Omics and Antiviral Properties to SARS-CoV-2 #MMPMID35401544
  • Tasli NP; Gonen ZB; Kirbas OK; Gokdemir NS; Bozkurt BT; Bayrakci B; Sagrac D; Taskan E; Demir S; Ekimci Gurcan N; Bayindir Bilgic M; Bayrak OF; Yetiskin H; Kaplan B; Pavel STI; Dinc G; Serhatli M; Cakirca G; Eken A; Aslan V; Yay M; Karakukcu M; Unal E; Gul F; Basaran KE; Ozkul Y; Sahin F; Jones OY; Tekin S; Ozdarendeli A; Cetin M
  • Front Immunol 2022[]; 13 (ä): 824378 PMID35401544show ga
  • The scale of the COVID-19 pandemic forced urgent measures for the development of new therapeutics. One of these strategies is the use of convalescent plasma (CP) as a conventional source for passive immunity. Recently, there has been interest in CP-derived exosomes. In this report, we present a structural, biochemical, and biological characterization of our proprietary product, convalescent human immune plasma-derived exosome (ChipEXO), following the guidelines set forth by the Turkish Ministry of Health and the Turkish Red Crescent, the Good Manufacturing Practice, the International Society for Extracellular Vesicles, and the Gene Ontology Consortium. The data support the safety and efficacy of this product against SARS-CoV-2 infections in preclinical models.
  • |*COVID-19/therapy[MESH]
  • |*Exosomes[MESH]
  • |Antibodies, Viral[MESH]
  • |Antiviral Agents/therapeutic use[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |Humans[MESH]
  • |Immunization, Passive[MESH]
  • |Pandemics[MESH]


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