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Accuracy of quantitative viral secondary standards: a re-examination.
Hayden, R T; Su, Y; Tang, L; Zhu, H; Gu, Z; Glasgow, H L; Sam, S S; Caliendo, A M.
  • Hayden RT; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Su Y; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Tang L; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Zhu H; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Gu Z; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Glasgow HL; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Sam SS; Division of Infectious Diseases, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
  • Caliendo AM; Department of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
J Clin Microbiol ; 62(3): e0166923, 2024 03 13.
Article en En | MEDLINE | ID: mdl-38380932
ABSTRACT
Interlaboratory agreement of viral load assays depends on the accuracy and uniformity of quantitative calibrators. Previous work demonstrated poor agreement of secondary cytomegalovirus (CMV) standards with nominal values. This study re-evaluated this issue among commercially produced secondary standards for both BK virus (BKV) and CMV, using digital polymerase chain reaction (dPCR) to compare the materials from three different manufacturers. Overall, standards showed an improved agreement compared to prior work, against nominal values in both log10 copies/mL and log10 international unit (IU)/mL, with bias from manufacturer-assigned nominal values of 0.0-0.9 log10 units (either copies or IU)/mL. Standards normalized to IU and those values assigned by dPCR rather than by real-time PCR (qPCR) showed better agreement with nominal values. The latter reinforces prior conclusions regarding the utility of using such methods for quantitative value assignment in reference materials. Quantitative standards have improved over the last several years, and the remaining bias from nominal values might be further reduced by universal implementation of dPCR methods for value assignment, normalized to IU. IMPORTANCE Interlaboratory agreement of viral load assays depends on accuracy and uniformity of quantitative calibrators. Previous work, published in JCM several years ago, demonstrated poor agreement of secondary cytomegalovirus (CMV) standards with nominal values. This study re-evaluated this issue among commercially produced secondary standards for both BK virus (BKV) and CMV, using digital polymerase chain reaction (dPCR) to compare the materials from three different manufacturers. Overall, standards showed an improved agreement compared to prior work, against nominal values, indicating a substantial improvement in the production of accurate secondary viral standards, while supporting the need for further work in this area and for the broad adaption of international unit (IU) as a reporting standard for quantitative viral load results.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virus BK / Infecciones por Citomegalovirus Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virus BK / Infecciones por Citomegalovirus Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article