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10.3390/ijms22052723

http://scihub22266oqcxt.onion/10.3390/ijms22052723
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33800363!7962843!33800363
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suck abstract from ncbi


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pmid33800363      Int+J+Mol+Sci 2021 ; 22 (5): ä
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  • Towards Quantitative and Standardized Serological and Neutralization Assays for COVID-19 #MMPMID33800363
  • Tian L; Elsheikh EB; Patrone PN; Kearsley AJ; Gaigalas AK; Inwood S; Lin-Gibson S; Esposito D; Wang L
  • Int J Mol Sci 2021[Mar]; 22 (5): ä PMID33800363show ga
  • Quantitative and robust serology assays are critical measurements underpinning global COVID-19 response to diagnostic, surveillance, and vaccine development. Here, we report a proof-of-concept approach for the development of quantitative, multiplexed flow cytometry-based serological and neutralization assays. The serology assays test the IgG and IgM against both the full-length spike antigens and the receptor binding domain (RBD) of the spike antigen. Benchmarking against an RBD-specific SARS-CoV IgG reference standard, the anti-SARS-CoV-2 RBD antibody titer was quantified in the range of 37.6 microg/mL to 31.0 ng/mL. The quantitative assays are highly specific with no correlative cross-reactivity with the spike proteins of MERS, SARS1, OC43 and HKU1 viruses. We further demonstrated good correlation between anti-RBD antibody titers and neutralizing antibody titers. The suite of serology and neutralization assays help to improve measurement confidence and are complementary and foundational for clinical and epidemiologic studies.
  • |Antibodies, Neutralizing/blood/immunology[MESH]
  • |Antibodies, Viral/blood/immunology[MESH]
  • |COVID-19 Serological Testing/*methods/*standards[MESH]
  • |COVID-19/*blood/*immunology[MESH]
  • |Cross Reactions[MESH]
  • |Flow Cytometry/methods[MESH]
  • |Fluorescence[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/blood/immunology[MESH]
  • |Immunoglobulin M/blood/immunology[MESH]
  • |Microspheres[MESH]
  • |Neutralization Tests/*methods/*standards[MESH]
  • |Receptors, Virus/chemistry/immunology[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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