Distinct Inflammatory Programs Underlie the Intramuscular Lipid Nanoparticle Response
Developments in mRNA/lipid nanoparticle (LNP) technology have advanced the fields of vaccinology and gene therapy, raising questions about immunogenicity. While some mRNA/LNPs generate an adjuvant-like environment in muscle tissue, other mRNA/LNPs are distinct in their capacity for multiple rounds of therapeutic delivery. We evaluate the adjuvancy of components of mRNA/LNPs by phenotyping cellular infiltrate at injection sites, tracking uptake by immune cells, and assessing the inflammatory state. Delivery of 9 common, but chemically distinct, LNPs to muscle revealed two classes of inflammatory gene expression programs: inflammatory (Class A) and noninflammatory (Class B). We find that intramuscular injection with Class A, but not Class B, empty LNPs (eLNPs) induce robust neutrophil infiltration into muscle within 2 h and a diverse myeloid population within 24 h. Single-cell RNA sequencing revealed SM-102-mediated expression of inflammatory chemokines by myeloid infiltrates within muscle 1 day after injection. Surprisingly, we found direct transfection of muscle infiltrating myeloid cells and splenocytes 24 h after intramuscular mRNA/LNP administration. Transfected myeloid cells within the muscle exhibit an activated phenotype 24 h after injection. Similarly, directly transfected splenic lymphocytes and dendritic cells (DCs) are differentially activated by Class A or Class B containing mRNA/LNP. Within the splenic DC compartment, type II conventional DCs (cDC2s) are directly transfected and activated by Class A mRNA/LNP. Together, we show that mRNA and LNPs work synergistically to provide the necessary innate immune stimuli required for effective vaccination. Importantly, this work provides a design framework for vaccines and therapeutics alike.
Authors
- Amber L. Doiron (ORCID: https://orcid.org/0000-0002-6963-0989)
- Somen K Mistri (ORCID: https://orcid.org/0000-0002-2139-6927)
- Emily R. Clark
- Michael J. Toth (ORCID: https://orcid.org/0000-0003-0668-1911)
- Jonathan E. Boyson (ORCID: https://orcid.org/0000-0003-2673-9148)
- Matthew E. Poynter (ORCID: https://orcid.org/0000-0002-7578-4570)
- Deena B. Snoke (ORCID: https://orcid.org/0000-0003-2189-9441)
- Sylvester Languon (ORCID: https://orcid.org/0000-0001-9924-9006)
- Jacob Dearborn (ORCID: https://orcid.org/0000-0001-8894-1574)
- William Dowell
- Devdoot Majumdar (ORCID: https://orcid.org/0000-0002-2541-3851)
- Kalev Freeman (ORCID: https://orcid.org/0000-0003-4817-2955)
- Zachary D. Miller
- Stephen Paige (ORCID: https://orcid.org/0000-0003-0089-3438)
- Amy Schumer
- Ethan Harby
- Adam B. Zuchowski
- Carlos Lescieur-Garcia
- Jesse Vix
- Tylar Kirch
- Olivia Garvin
- Lily Kjendal
Institutions
- University of Vermont (US)
- University of Vermont Medical Center (US)
Publication Details
- Journal
- ACS Nano
- Published
- 2024-11-20
- DOI
- https://doi.org/10.1021/acsnano.4c08490
- Citations
- 10
- Primary Topic
- Reproductive System and Pregnancy
- Type
- article
- Field-Weighted Citation Impact
- 2.40
Funders
- National Institutes of Health
- Larner College of Medicine, University of Vermont
- National Heart, Lung, and Blood Institute
- National Institute of General Medical Sciences