Development and Characterization of a Ten-Plex Assay to Measure Klebsiella pneumoniae Antigen-Specific IgG in Human Sera

<i>Klebsiella pneumoniae</i> is a leading cause of nosocomial infections, neonatal sepsis, and childhood mortality worldwide. A drastic rise in antibiotic-resistant isolates poses an urgent threat to humanity, and the World Health Organization (WHO) has classified this as a critical-priority antimicrobial-resistant (AMR) pathogen. Recent advancements in developing vaccines against <i>Klebsiella pneumoniae</i> have highlighted the lack of standardized assays to evaluate immunogenicity, complicating comparison among different vaccines under development and the establishment of a serological threshold of risk reduction (SToRR). Here, we describe the development of a ten-plex multiplex assay to measure IgG against capsular polysaccharides (K2, K25, K102, K149), O antigens (O1v1, O1v2, O2v1, O2v2 and O5), and a conserved protein (MrkA). A standard curve was established by pooling human sera from naturally exposed subjects and then calibrated in terms of Relative Luminex Units/mL. The assay was fully characterized in terms of specificity, precision, linearity, and repeatability. This immunoassay demonstrates performance suitable for future clinical trials, as well as to perform sero-epidemiological studies to gain insights into naturally occurring immunity, potentially contributing to the establishment of a serological threshold of risk reduction against <i>Klebsiella pneumoniae</i>.

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Publication Details

Journal
Methods and Protocols
Published
2025-05-19
DOI
https://doi.org/10.3390/mps8030052
Citations
1
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.59

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article

Development and Characterization of a Ten-Plex Assay to Measure Klebsiella pneumoniae Antigen-Specific IgG in Human Sera

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1 citations
Methods and Protocols
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article

Development and Characterization of a Ten-Plex Assay to Measure Klebsiella pneumoniae Antigen-Specific IgG in Human Sera

Denasha L. Reddy, Luca Rovetini, Heena Ranchod, Makrina Totsika, Omar Rossi, Renzo Alfini, Mariagrazia Molfetta, Davide Oldrini, Carlo Giannelli, Francesca Micoli, Luisa Massai, Francesca Nonne, Miren Iturriza‐Gómara, Shabir Ahmed Madhi, Martina Carducci, Ziyaad Dangor, Gianina Florentina Belciug
article en
1 citations

Abstract

<i>Klebsiella pneumoniae</i> is a leading cause of nosocomial infections, neonatal sepsis, and childhood mortality worldwide. A drastic rise in antibiotic-resistant isolates poses an urgent threat to humanity, and the World Health Organization (WHO) has classified this as a critical-priority antimicrobial-resistant (AMR) pathogen. Recent advancements in developing vaccines against <i>Klebsiella pneumoniae</i> have highlighted the lack of standardized assays to evaluate immunogenicity, complicating comparison among different vaccines under development and the establishment of a serological threshold of risk reduction (SToRR). Here, we describe the development of a ten-plex multiplex assay to measure IgG against capsular polysaccharides (K2, K25, K102, K149), O antigens (O1v1, O1v2, O2v1, O2v2 and O5), and a conserved protein (MrkA). A standard curve was established by pooling human sera from naturally exposed subjects and then calibrated in terms of Relative Luminex Units/mL. The assay was fully characterized in terms of specificity, precision, linearity, and repeatability. This immunoassay demonstrates performance suitable for future clinical trials, as well as to perform sero-epidemiological studies to gain insights into naturally occurring immunity, potentially contributing to the establishment of a serological threshold of risk reduction against <i>Klebsiella pneumoniae</i>.

Methods and ProtocolsVol. 8(3)
South African Medical Research Council (ZA), University of the Witwatersrand (ZA)
Bill and Melinda Gates Foundation, Pfizer, AstraZeneca
Good health and well-being
Openalex Percentile: Top 36%
Antibiotic Resistance in Bacteria
0.59
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