AI Article Synopsis

  • A standardized multiplex immunoassay for measuring IgG antibodies against group B streptococcus (GBS) capsular polysaccharide (CPS) is essential for evaluating maternal GBS vaccines and establishing protection correlates in infants.
  • An interlaboratory study involving five labs used consistent reagents and protocols with 44 human sera, achieving good precision and reproducibility across all six GBS serotypes.
  • The study confirmed the assay's robustness, showing that anti-CPS IgG concentrations were reliably produced across different laboratories when following standardized methods.

Article Abstract

Measurement of IgG antibodies against group B streptococcus (GBS) capsular polysaccharide (CPS) by use of a standardized and internationally accepted multiplex immunoassay is important for the evaluation of candidate maternal GBS vaccines in order to compare results across studies. A standardized assay is also required if serocorrelates of protection against invasive GBS disease are to be established in infant sera for the six predominant GBS serotypes since it would permit the comparison of results across the six serotypes. We undertook an interlaboratory study across five laboratories that used standardized assay reagents and protocols with a panel of 44 human sera to measure IgG antibodies against GBS CPS serotypes Ia, Ib, II, III, IV, and V. The within-laboratory intermediate precision, which included factors like the lot of coated beads, laboratory analyst, and day, was generally below 20% relative standard deviation (RSD) for all six serotypes, across all five laboratories. The cross-laboratory reproducibility was < 25% RSD for all six serotypes, which demonstrated the consistency of results across the different laboratories. Additionally, anti-CPS IgG concentrations for the 44-member human serum panel were established. The results of this study showed assay robustness and that the resultant anti-CPS IgG concentrations were reproducible across laboratories for the six GBS CPS serotypes when the standardized assay was used.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11018077PMC
http://dx.doi.org/10.1080/21645515.2024.2330138DOI Listing

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