Klebsiella pneumoniae bioconjugate vaccine functional durability in mice

Klebsiella pneumoniae is a leading cause of hospital-acquired infections as well as the leading cause of neonatal sepsis worldwide. Further, increasing antibiotic resistance in this pathogen makes K. pneumoniae troublesome to treat. Despite its clinical importance, there is not yet an approved K. pneumoniae vaccine available. Here we tested antibody durability and long-term functionality of two previously reported bioconjugate vaccines targeting the K. pneumoniae capsular type K2 and O-antigen type O1v1. We demonstrate that both antibodies are durable in mice for up to six months with significant IgG titers. However, only the K2 antibodies exhibit functionality out to six months as evidenced by serum bactericidal activity and survival in a murine bacteremia challenge model. These results are another promising step towards demonstrating the clinical capacity of bioconjugate vaccines and their induction of durable antibody responses.

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Publication Details

Journal
Vaccine
Published
2024-11-20
DOI
https://doi.org/10.1016/j.vaccine.2024.126536
Citations
13
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
2.21

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article

Klebsiella pneumoniae bioconjugate vaccine functional durability in mice

Cory J. Knoot, Paeton L. Wantuch, Christian M. Harding, David A. Rosen et al.
13 citations
Vaccine
Antibiotic Resistance in Bacteria
2.21
article

Klebsiella pneumoniae bioconjugate vaccine functional durability in mice

Cory J. Knoot, Paeton L. Wantuch, Christian M. Harding, David A. Rosen, Emily C. Marino
article en
13 citations

Abstract

Klebsiella pneumoniae is a leading cause of hospital-acquired infections as well as the leading cause of neonatal sepsis worldwide. Further, increasing antibiotic resistance in this pathogen makes K. pneumoniae troublesome to treat. Despite its clinical importance, there is not yet an approved K. pneumoniae vaccine available. Here we tested antibody durability and long-term functionality of two previously reported bioconjugate vaccines targeting the K. pneumoniae capsular type K2 and O-antigen type O1v1. We demonstrate that both antibodies are durable in mice for up to six months with significant IgG titers. However, only the K2 antibodies exhibit functionality out to six months as evidenced by serum bactericidal activity and survival in a murine bacteremia challenge model. These results are another promising step towards demonstrating the clinical capacity of bioconjugate vaccines and their induction of durable antibody responses.

VaccineVol. 43(Pt 2)
Washington University in St. Louis (US)
National Institutes of Health, National Institute of Allergy and Infectious Diseases
Zero hunger
Openalex Percentile: Top 11%
Antibiotic Resistance in Bacteria
2.21
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