Transfer of anti-Klebsiella pneumoniae immunity following infection in mice is protective against lethal challenge in offspring

Klebsiella pneumoniae is a gram-negative, opportunistic pathogen, with high rates of antimicrobial resistance, and is responsible for a wide range of infections of the urinary tract, lungs, and bloodstream, among others. Disease burden is particularly high in neonates, where K. pneumoniae is a leading cause of sepsis. Renewed interest in vaccine development against this critical priority pathogen has focused on this vulnerable population. Vaccination in pregnancy is a promising approach for prevention of neonatal sepsis, however efforts to understand the dynamics, specificity and function of maternally transferred antibodies is ongoing. We report here that K. pneumoniae-specific IgG is readily transferred from dam to pup following wild-type infection in mice, and that maternally-transferred immunity is protective against lethal infection in pups aged 6 weeks. Further work to investigate the mechanisms of protection and explore neonatal challenge models will advance the path to a maternal vaccine to protect against neonatal sepsis.

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Publication Details

Journal
Scientific Reports
Published
2026-01-08
DOI
https://doi.org/10.1038/s41598-025-33619-x
Primary Topic
Bacterial Infections and Vaccines
Type
article
Field-Weighted Citation Impact
0.00

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article

Transfer of anti-Klebsiella pneumoniae immunity following infection in mice is protective against lethal challenge in offspring

R V Patel, Kaitlin Winter, Mandy Lo, Ken Chu et al.
Scientific Reports
Bacterial Infections and Vaccines
article

Transfer of anti-Klebsiella pneumoniae immunity following infection in mice is protective against lethal challenge in offspring

R V Patel, Kaitlin Winter, Mandy Lo, Ken Chu, Emily Mason, Hennady P. Shulha, Tony Harn, Sina Hakimpour, Bing Cai, Jiawei Liang
article en

Abstract

Klebsiella pneumoniae is a gram-negative, opportunistic pathogen, with high rates of antimicrobial resistance, and is responsible for a wide range of infections of the urinary tract, lungs, and bloodstream, among others. Disease burden is particularly high in neonates, where K. pneumoniae is a leading cause of sepsis. Renewed interest in vaccine development against this critical priority pathogen has focused on this vulnerable population. Vaccination in pregnancy is a promising approach for prevention of neonatal sepsis, however efforts to understand the dynamics, specificity and function of maternally transferred antibodies is ongoing. We report here that K. pneumoniae-specific IgG is readily transferred from dam to pup following wild-type infection in mice, and that maternally-transferred immunity is protective against lethal infection in pups aged 6 weeks. Further work to investigate the mechanisms of protection and explore neonatal challenge models will advance the path to a maternal vaccine to protect against neonatal sepsis.

Scientific ReportsVol. 16(1)
University of British Columbia Hospital (CA), University of British Columbia (CA), BC Children's Hospital (CA)
Children's Hospital Foundation, BC Children's Hospital, Canadian Lung Association, Michael Smith Health Research BC, European Society of Clinical Microbiology and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 93%
Bacterial Infections and Vaccines
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