Monitoring mRNA vaccine antigen expression in vivo using PET/CT

Noninvasive visualization of the distribution and persistence of mRNA vaccine antigen expression in mammalian systems has implications for the development and evaluation of future mRNA vaccines. Here, we genetically fuse E. coli dihydrofolate reductase (eDHFR) to the delta furin diproline modified SARS-CoV-2 spike glycoprotein (S2P<sup>∆f</sup>) mRNA vaccine and image its expression in female mice and male non-human primates using [<sup>18</sup>F]fluoropropyl-trimethoprim ([<sup>18</sup>F]FP-TMP). Whole body positron emission tomography (PET) imaging revealed transient expression of the vaccine antigen in the injection site and draining lymph nodes (dLNs). Fusion of eDHFR did not impact S2P immunogenicity and no humoral or cellular immune response was detected against eDHFR in either species. In this work, we show that eDHFR can be used as an mRNA-encoded PET reporter gene to monitor the spatiotemporal dynamics of mRNA vaccine antigen expression in vivo. This technique could be applied in clinical translation of future mRNA vaccines or therapeutics.

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Publication Details

Journal
Nature Communications
Published
2025-03-06
DOI
https://doi.org/10.1038/s41467-025-57446-w
Citations
13
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
10.37

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article

Monitoring mRNA vaccine antigen expression in vivo using PET/CT

Marc Lavertu, Jean M. Etersque, Robert H. Mach, Gabrielle S. Blizard et al.
13 citations
Nature Communications
Immunotherapy and Immune Responses
10.37
article

Monitoring mRNA vaccine antigen expression in vivo using PET/CT

Marc Lavertu, Jean M. Etersque, Robert H. Mach, Gabrielle S. Blizard, Benjamin Davis, Garima Dwivedi, Quy Cao, Mark A. Sellmyer, Ying K. Tam, Anik Chevrier, Mohamad‐Gabriel Alameh, Houping Ni, Catherine Hou, Yi‐Gen Pan, Hooda Said
article en
13 citations

Abstract

Noninvasive visualization of the distribution and persistence of mRNA vaccine antigen expression in mammalian systems has implications for the development and evaluation of future mRNA vaccines. Here, we genetically fuse E. coli dihydrofolate reductase (eDHFR) to the delta furin diproline modified SARS-CoV-2 spike glycoprotein (S2P<sup>∆f</sup>) mRNA vaccine and image its expression in female mice and male non-human primates using [<sup>18</sup>F]fluoropropyl-trimethoprim ([<sup>18</sup>F]FP-TMP). Whole body positron emission tomography (PET) imaging revealed transient expression of the vaccine antigen in the injection site and draining lymph nodes (dLNs). Fusion of eDHFR did not impact S2P immunogenicity and no humoral or cellular immune response was detected against eDHFR in either species. In this work, we show that eDHFR can be used as an mRNA-encoded PET reporter gene to monitor the spatiotemporal dynamics of mRNA vaccine antigen expression in vivo. This technique could be applied in clinical translation of future mRNA vaccines or therapeutics.

Nature CommunicationsVol. 16(1)
Children's Hospital of Philadelphia (US), Penn Center for AIDS Research (US), Acuitas Therapeutics (Canada) (CA), Polytechnique Montréal (CA), University of Pennsylvania (US)
Burroughs Wellcome Fund, Cancer Research Institute, NIH Office of the Director, National Institute of General Medical Sciences
Openalex Percentile: Top 1%
Immunotherapy and Immune Responses
10.37
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