Harmonization of Multiple SARS-CoV-2 Reference Materials Using the WHO IS (NIBSC 20/136): Results and Implications

被引:6
作者
Windsor, William Jonathan [1 ]
Roell, Yannik [1 ]
Tucker, Heidi [2 ]
Cheng, Chi-An [3 ]
Suliman, Sara [4 ,5 ]
Peek, Laura J. [6 ]
Pestano, Gary A. [6 ]
Lee, William T. [2 ]
Zeichhardt, Heinz [7 ,8 ,9 ]
Lamb, Molly M. [1 ]
Kammel, Martin [7 ,8 ,9 ]
Wang, Hui [10 ]
Kedl, Ross [11 ]
Rester, Cody [11 ]
Morrison, Thomas E. [11 ]
Davenport, Bennet J. [11 ]
Carson, Kyle [2 ]
Yates, Jennifer [2 ]
Howard, Kelly [2 ]
Kulas, Karen [2 ]
Walt, David R. [3 ]
Dafni, Aner [12 ]
Taylor, Daniel [12 ]
Chu, May [1 ]
机构
[1] Colorado Sch Publ Hlth, Ctr Global Hlth, Aurora, CO 80045 USA
[2] Wadsworth Ctr, New York State Dept Hlth, Div Infect Dis, Albany, NY USA
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA USA
[4] Brigham & Womens Hosp, Harvard Med Sch, Div Rheumatol, Inflammat & Immun, Boston, MA USA
[5] Univ Calif San Francisco, Zuckerberg San Francisco Gen Hosp, Div Expt Med, San Francisco, CA USA
[6] Biodesix Inc, Boulder, CO USA
[7] INSTAND e V, Soc Promoting Qual Assurance Med Labs, Dusseldorf, Germany
[8] IQVD GmbH, Inst fuer Qualitaetssicherung Virusdiagnost, Berlin, Germany
[9] GBD Gesell fuer Biotechnol Diagnost mbH, Berlin, Germany
[10] Thermo Fisher Sci, Waltham, MA USA
[11] Univ Colorado Anschutz Med Campus, Dept Immunol, Aurora, CO USA
[12] Oneworld Accuracy, Vancouver, BC, Canada
基金
比尔及梅琳达.盖茨基金会;
关键词
SARS-CoV-2; serology; International Standards; concordance; immunology; harmonization; parallel-line assay; STANDARD;
D O I
10.3389/fmicb.2022.893801
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundThere is an urgent need for harmonization between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology platforms and assays prior to defining appropriate correlates of protection and as well inform the development of new rapid diagnostic tests that can be used for serosurveillance as new variants of concern (VOC) emerge. We compared multiple SARS-CoV-2 serology reference materials to the WHO International Standard (WHO IS) to determine their utility as secondary standards, using an international network of laboratories with high-throughput quantitative serology assays. This enabled the comparison of quantitative results between multiple serology platforms. MethodsBetween April and December 2020, 13 well-characterized and validated SARS-CoV-2 serology reference materials were recruited from six different providers to qualify as secondary standards to the WHO IS. All the samples were tested in parallel with the National Institute for Biological Standards and Control (NIBSC) 20/136 and parallel-line assays were used to calculate the relevant potency and binding antibody units. ResultsAll the samples saw varying levels of concordance between diagnostic methods at specific antigen-antibody combinations. Seven of the 12 candidate materials had high concordance for the spike-immunoglobulin G (IgG) analyte [percent coefficient of variation (%CV) between 5 and 44%]. ConclusionDespite some concordance between laboratories, qualification of secondary materials to the WHO IS using arbitrary international units or binding antibody units per milliliter (BAU/ml) does not provide any benefit to the reference materials overall, due to the lack of consistent agreeable international unit (IU) or BAU/ml conversions between laboratories. Secondary standards should be qualified to well-characterized reference materials, such as the WHO IS, using serology assays that are similar to the ones used for the original characterization of the WHO IS.
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页数:13
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