A multivalent mRNA-LNP vaccine protects against <i>Clostridioides difficile</i> infection

<i>Clostridioides difficile</i> infection (CDI) is an urgent public health threat with limited preventative options. In this work, we developed a messenger RNA (mRNA)-lipid nanoparticle (LNP) vaccine targeting <i>C. difficile</i> toxins and virulence factors. This multivalent vaccine elicited robust and long-lived systemic and mucosal antigen-specific humoral and cellular immune responses across animal models, independent of changes to the intestinal microbiota. Vaccination protected mice from lethal CDI in both primary and recurrent infection models, and inclusion of non-toxin cellular and spore antigens improved decolonization of toxigenic <i>C. difficile</i> from the gastrointestinal tract. Our studies demonstrate mRNA-LNP vaccine technology as a promising platform for the development of novel <i>C. difficile</i> therapeutics with potential for limiting acute disease and promoting bacterial decolonization.

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Publication Details

Journal
Science
Published
2024-10-03
DOI
https://doi.org/10.1126/science.adn4955
Citations
66
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
Field-Weighted Citation Impact
25.68

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article

A multivalent mRNA-LNP vaccine protects against Clostridioides difficile infection

Qianxuan She, Marc Lavertu, Robert H. Mach, Ceylan Tanes et al.
66 citations
Science
Clostridium difficile and Clostridium perfringens research
25.68
article

A multivalent mRNA-LNP vaccine protects against Clostridioides difficile infection

Qianxuan She, Marc Lavertu, Robert H. Mach, Ceylan Tanes, Paula C. Rangel, Gabrielle S. Blizard, Jeffrey R. Maslanka, James J. Knox, Paul J. Planet, Benjamin Davis, Emma E. Furth, Garima Dwivedi, Joseph P. Zackular, Nile U. Bayard, Mark A. Sellmyer, Ying K. Tam, Ahmed M. Moustafa, Kyle Bittinger, Anik Chevrier, Drew Weissman, Mohamad‐Gabriel Alameh, Houping Ni, Mitchell Beattie, Alexa Semon, Yi‐Gen Pan, Michael C. Abt, Haitao Hu, Rochelle C. Glover, Srinivasa Reddy Bonam
article en
66 citations

Abstract

<i>Clostridioides difficile</i> infection (CDI) is an urgent public health threat with limited preventative options. In this work, we developed a messenger RNA (mRNA)-lipid nanoparticle (LNP) vaccine targeting <i>C. difficile</i> toxins and virulence factors. This multivalent vaccine elicited robust and long-lived systemic and mucosal antigen-specific humoral and cellular immune responses across animal models, independent of changes to the intestinal microbiota. Vaccination protected mice from lethal CDI in both primary and recurrent infection models, and inclusion of non-toxin cellular and spore antigens improved decolonization of toxigenic <i>C. difficile</i> from the gastrointestinal tract. Our studies demonstrate mRNA-LNP vaccine technology as a promising platform for the development of novel <i>C. difficile</i> therapeutics with potential for limiting acute disease and promoting bacterial decolonization.

ScienceVol. 386(6717)
Children's Hospital of Philadelphia (US), American Museum of Natural History (US), Acuitas Therapeutics (Canada) (CA), Polytechnique Montréal (CA), The University of Texas Medical Branch at Galveston (US), University of Pennsylvania (US)
Children's Hospital of Philadelphia, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 0%
Clostridium difficile and Clostridium perfringens research
25.68
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