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10.1371/journal.pone.0253551

http://scihub22266oqcxt.onion/10.1371/journal.pone.0253551
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34310603!8312954!34310603
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suck abstract from ncbi


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pmid34310603      PLoS+One 2021 ; 16 (7): e0253551
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  • Predicting the efficacy of COVID-19 convalescent plasma donor units with the Lumit Dx anti-receptor binding domain assay #MMPMID34310603
  • Janaka SK; Clark NM; Evans DT; Mou H; Farzan M; Connor JP
  • PLoS One 2021[]; 16 (7): e0253551 PMID34310603show ga
  • BACKGROUND: The novel coronavirus SARS-CoV2 that causes COVID-19 has resulted in the death of more than 2.5 million people, but no cure exists. Although passive immunization with COVID-19 convalescent plasma (CCP) provides a safe and viable therapeutic option, the selection of optimal units for therapy in a timely fashion remains a barrier. STUDY DESIGN AND METHODS: Since virus neutralization is a necessary characteristic of plasma that can benefit recipients, the neutralizing titers of plasma samples were measured using a retroviral-pseudotype assay. Binding antibody titers to the spike (S) protein were also determined by a clinically available serological assay (Ortho-Vitros total IG), and an in-house ELISA. The results of these assays were compared to a measurement of antibodies directed to the receptor binding domain (RBD) of the SARS-CoV2 S protein (Promega Lumit Dx). RESULTS: All measures of antibodies were highly variable, but correlated, to different degrees, with each other. However, the anti-RBD antibodies correlated with viral neutralizing titers to a greater extent than the other antibody assays. DISCUSSION: Our observations support the use of an anti-RBD assay such as the Lumit Dx assay, as an optimal predictor of the neutralization capability of CCP.
  • |Angiotensin-Converting Enzyme 2/genetics/immunology[MESH]
  • |Antibodies, Neutralizing/*blood[MESH]
  • |Antibodies, Viral/*blood[MESH]
  • |Blood Donors[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19/diagnosis/immunology/*therapy/virology[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Gene Expression[MESH]
  • |Host-Pathogen Interactions/genetics/immunology[MESH]
  • |Humans[MESH]
  • |Immune Sera/chemistry[MESH]
  • |Immunization, Passive/methods[MESH]
  • |Immunoglobulin G/*blood[MESH]
  • |Neutralization Tests[MESH]
  • |Predictive Value of Tests[MESH]
  • |Protein Binding[MESH]
  • |Protein Domains[MESH]
  • |SARS-CoV-2/*immunology/pathogenicity[MESH]


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