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  1. Article: Performance of the 4Kscore Test in Plasma and Serum and Stability of the Component Analytes in Clinical Samples.

    Higgins, Christina E / Neybold, Patricia / Holdridge, Marcella B / Barnes, Catherine R / Dong, Yan / Reeve, Michael / Mathur, Vinita / Weisberger, James / Linder, Vincent

    The journal of applied laboratory medicine

    2021  Volume 3, Issue 2, Page(s) 185–199

    Abstract: Background: The 4Kscore Test determines a personalized risk score for aggressive prostate cancer by combining the blood sample measurements of total prostate-specific antigen (tPSA), free PSA (fPSA), intact PSA (iPSA), and human kallikrein-related ... ...

    Abstract Background: The 4Kscore Test determines a personalized risk score for aggressive prostate cancer by combining the blood sample measurements of total prostate-specific antigen (tPSA), free PSA (fPSA), intact PSA (iPSA), and human kallikrein-related peptidase 2 (hK2) with patient clinical information to generate the patient risk's score; thus, accuracy and precision of the 4Kscore depend on the reliability of these measurements. Although tPSA and fPSA are measured on a Food and Drug Administration (FDA)-approved platform, the performance of the iPSA and hK2 assays in the clinical setting has not previously been reported.
    Methods: Analytical performance was determined for the iPSA and hK2 assays in both serum and EDTA plasma, according to Clinical and Laboratory Standards Institute guidelines. Equivalence of the 4Kscore in both sample matrices was demonstrated in a 353-patient clinical cohort, and the stability of endogenous iPSA and hK2 for at least 3 days was demonstrated in a smaller subset.
    Results: Intralaboratory and interlaboratory precision of the iPSA and hK2 assays in both matrices was comparable with that of FDA-approved tPSA and fPSA assays (<18% for iPSA; <8% for hK2). The picogram per milliliter sensitivity and wide dynamic range of the iPSA and hK2 assays allowed for accurate measurements in the target population. The 4Kscore generated in either matrix up to 3 days after collection is equivalent to that measured within 24 h of collection (Passing-Bablok slope 95% CI: plasma, 0.999-1.034; serum, 0.997-1.040).
    Conclusions: The robust performance of component assays and reliable stability of the endogenous analytes in clinical samples proven here ensures an accurate 4Kscore Test result.
    Language English
    Publishing date 2021-01-26
    Publishing country England
    Document type Journal Article
    ISSN 2576-9456
    ISSN 2576-9456
    DOI 10.1373/jalm.2017.024612
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: N-protein presents early in blood, dried blood and saliva during asymptomatic and symptomatic SARS-CoV-2 infection.

    Shan, Dandan / Johnson, Joseph M / Fernandes, Syrena C / Suib, Hannah / Hwang, Soyoon / Wuelfing, Danica / Mendes, Muriel / Holdridge, Marcella / Burke, Elaine M / Beauregard, Katie / Zhang, Ying / Cleary, Megan / Xu, Samantha / Yao, Xiao / Patel, Purvish P / Plavina, Tatiana / Wilson, David H / Chang, Lei / Kaiser, Kim M /
    Nattermann, Jacob / Schmidt, Susanne V / Latz, Eicke / Hrusovsky, Kevin / Mattoon, Dawn / Ball, Andrew J

    Nature communications

    2021  Volume 12, Issue 1, Page(s) 1931

    Abstract: The COVID-19 pandemic continues to have an unprecedented impact on societies and economies worldwide. There remains an ongoing need for high-performance SARS-CoV-2 tests which may be broadly deployed for infection monitoring. Here we report a highly ... ...

    Abstract The COVID-19 pandemic continues to have an unprecedented impact on societies and economies worldwide. There remains an ongoing need for high-performance SARS-CoV-2 tests which may be broadly deployed for infection monitoring. Here we report a highly sensitive single molecule array (Simoa) immunoassay in development for detection of SARS-CoV-2 nucleocapsid protein (N-protein) in venous and capillary blood and saliva. In all matrices in the studies conducted to date we observe >98% negative percent agreement and >90% positive percent agreement with molecular testing for days 1-7 in symptomatic, asymptomatic, and pre-symptomatic PCR+ individuals. N-protein load decreases as anti-SARS-CoV-2 spike-IgG increases, and N-protein levels correlate with RT-PCR Ct-values in saliva, and between matched saliva and capillary blood samples. This Simoa SARS-CoV-2 N-protein assay effectively detects SARS-CoV-2 infection via measurement of antigen levels in blood or saliva, using non-invasive, swab-independent collection methods, offering potential for at home and point of care sample collection.
    MeSH term(s) COVID-19/diagnosis ; COVID-19/epidemiology ; COVID-19/virology ; COVID-19 Testing/methods ; Coronavirus Nucleocapsid Proteins/blood ; Coronavirus Nucleocapsid Proteins/genetics ; Epidemics ; Home Care Services ; Humans ; Point-of-Care Systems ; ROC Curve ; SARS-CoV-2/genetics ; SARS-CoV-2/metabolism ; SARS-CoV-2/physiology ; Saliva/virology ; Specimen Handling/methods
    Chemical Substances Coronavirus Nucleocapsid Proteins
    Language English
    Publishing date 2021-03-26
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-021-22072-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: SARS-Coronavirus-2 nucleocapsid protein measured in blood using a Simoa ultra-sensitive immunoassay differentiates COVID-19 infection with high clinical sensitivity.

    Shan, Dandan / Johnson, Joseph M / Fernandes, Syrena C / Mendes, Muriel / Suib, Hannah / Holdridge, Marcella / Burke, Elaine M / Beauregard, Katie G / Zhang, Ying / Cleary, Megan / Xu, Samantha / Yao, Xiao / Patel, Purvish P / Plavina, Tatiana / Wilson, David H / Chang, Lei / Kaiser, Kim M / Natterman, Jacob / Schmidt, Susanne V /
    Latz, Eicke / Hrusovsky, Kevin / Mattoon, Dawn / Ball, Andrew J

    medRxiv

    Abstract: The COVID-19 pandemic continues to have an unprecedented impact on societies and economies worldwide. Despite rapid advances in diagnostic test development and scale-up, there remains an ongoing need for SARS-CoV-2 tests which are highly sensitive, ... ...

    Abstract The COVID-19 pandemic continues to have an unprecedented impact on societies and economies worldwide. Despite rapid advances in diagnostic test development and scale-up, there remains an ongoing need for SARS-CoV-2 tests which are highly sensitive, specific, minimally invasive, cost-effective and scalable for broad testing and surveillance. Here we report development of a highly sensitive single molecule array (Simoa) immunoassay on the automated HD-X platform for the detection of SARS-CoV-2 Nucleocapsid protein (N-protein) in venous and capillary blood (fingerstick). In pre-pandemic and clinical sample sets, the assay has 100% specificity and 97.4% sensitivity for serum / plasma samples. The limit of detection (LoD) estimated by titration of inactivated SARS-CoV-2 virus is 0.2 pg/ml, corresponding to 0.05 Median Tissue Culture Infectious Dose (TCID50) per ml, > 2000 times more sensitive than current EUA approved antigen tests. No cross-reactivity to other common respiratory viruses, including hCoV229E, hCoVOC43, hCoVNL63, Influenza A or Influenza B, was observed. We detected elevated N-protein concentrations in symptomatic, asymptomatic, and pre-symptomatic PCR+ individuals using capillary blood from a finger-stick collection device. The Simoa SARS-CoV-2 N-protein assay has the potential to detect COVID-19 infection via antigen in blood with similar or better performance characteristics of molecular tests, while also enabling at home and point of care sample collection.
    Keywords covid19
    Language English
    Publishing date 2020-08-17
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2020.08.14.20175356
    Database COVID19

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