Fighting against Klebsiella pneumoniae: vaccine for prevention of antibiotic resistant infections.
Palabras clave:
AMR (antimicrobial resistance), vaccine, Klebsiella pneumoniaeResumen
The World Health Organization recognises antimicrobial resistance (AMR) as one of the top 10 threats to human health. The
pathogens commonly implicated in AMR infections are known as ESKAPE pathogens, where we find Klebsiella pneumoniae. It
is a highly antibiotic-resistant opportunistic Enterobacteriaceae leading to a variety of diseases due to urinary-tract-infections,
nosocomial, pneumonia, intra-abdominal infections and surgical wound infections that can potentially cause bacteremia and
septicemia. Furthermore, it is the leading cause of neonatal sepsis worldwide.
Klebsiella pneumoniae is causing 650.000 deaths worldwide associated with antibiotic-resistance, focusing in neonates and
elderly population affected by chronic diseases. Therefore, the focus of vaccine development has moved to preventing infections
that occur throughout all life stages by bacterial vaccines. One of these is K-vax. It is a modified inactivated whole cell bacterial
vaccine, under development by Vaxdyn.
In K-Vax, the major antigens leading to protective immunity are four full-length outer-membrane proteins (OMPs) expressed in
a LPS-null inactivated Acinetobacter baumannii carrier cell. For vaccine approval by regulatory authorities, probing the
mechanism of action of the vaccine and showing the contribution of the key antigens is essential.
In this work, first, we have analyzed the data presented previously by similar marketed vaccines to defend the mechanism of
action before engaging in human clinical trials. Then, we have gathered the immunogenicity data available for K-Vax to present
a proposal for mechanism of action. In particular, we have demonstrated that vaccination of animal models, including mice and
rabbits, leads to a specific humoral response against K. pneumoniae OMPs. The antisera carries functional antibodies able to
opsonize and promote killing of K. pneumoniae cells by complement or human phagocytes. The mechanism of action is effective
against several K. pneumoniae clinical strains, including hypervirulent strains, showing the high strain coverage of the vaccine
K-Vax.
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Hoppe, S., Bier, F. F., & Von Nickisch-Rosenegk, M. (2014). Identification of antigenic proteins of the nosocomial pathogen klebsiella pneumoniae. PLoS ONE, 9(10). https://doi.org/10.1371/journal.pone.0110703
Kumar, C. K., Sands, K., Walsh, T. R., OBrien, S., Sharland, M., Lewnard, J. A., Hu, H., Srikantiah, P., & Laxminarayan, R. (2023). Global, regional, and national estimates of the impact of a maternal Klebsiella pneumoniae vaccine: A Bayesian modeling analysis. PLoS Medicine, 20(5), 1–17. https://doi.org/10.1371/journal.pmed.1004239
Poolman, J. T. (2020). Expanding the role of bacterial vaccines into life-course vaccination strategies and prevention of antimicrobial-resistant infections. Npj Vaccines, 5(1). https://doi.org/10.1038/s41541-020-00232-0
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Derechos de autor 2024 Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria

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