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10.2217/imt-2020-0263

http://scihub22266oqcxt.onion/10.2217/imt-2020-0263
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33557591!7871744!33557591
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suck abstract from ncbi


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pmid33557591      Immunotherapy 2021 ; 13 (5): 397-407
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  • Production of hyperimmune anti-SARS-CoV-2 intravenous immunoglobulin from pooled COVID-19 convalescent plasma #MMPMID33557591
  • Ali S; Uddin SM; Ali A; Anjum F; Ali R; Shalim E; Khan M; Ahmed I; M Muhaymin S; Bukhari U; Luxmi S; Khan AS; Quraishy S
  • Immunotherapy 2021[Apr]; 13 (5): 397-407 PMID33557591show ga
  • Background: This study assesses the feasibility of producing hyperimmune anti-COVID-19 intravenously administrable immunoglobulin (C-IVIG) from pooled convalescent plasma (PCP) to provide a safe and effective passive immunization treatment option for COVID-19. Materials & methods: PCP was fractionated by modified caprylic acid precipitation followed by ultrafiltration/diafiltration to produce hyperimmune C-IVIG. Results: In C-IVIG, the mean SARS-CoV-2 antibody level was found to be threefold (104 +/- 30 cut-off index) that of the PCP (36 +/- 8.5 cut-off index) and mean protein concentration was found to be 46 +/- 3.7 g/l, comprised of 89.5% immunoglobulins. Conclusion: The current method of producing C-IVIG is feasible as it uses locally available PCP and simpler technology and yields a high titer of SARS-CoV-2 antibody. The safety and efficacy of C-IVIG will be evaluated in a registered clinical trial (NCT04521309).
  • |Antibodies, Viral/immunology/*isolation & purification/therapeutic use[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19/*blood/therapy[MESH]
  • |Caprylates/chemistry[MESH]
  • |Chemical Fractionation[MESH]
  • |Humans[MESH]
  • |Immunization, Passive[MESH]
  • |Immunoglobulins, Intravenous/immunology/*isolation & purification/therapeutic use[MESH]


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