An mRNA platform to create isolated, monospecific Th1 responses
Helper T cells (CD4 T cells) are lynchpins of adaptive immune responses. Each CD4 T cell expresses a single T-cell receptor, recognizing an epitope presented by major histocompatibility complex class II (MHC-II). Due to the enormous diversity of the T-cell repertoire, it is often desirable to study a population that responds to the same epitope. Here, we devised a novel method of selective immunization to produce a robust, monospecific helper T-cell response in mice using a modular mRNA vector. The vector encodes the target epitope attached via flexible linker to MHC-II. Immunization with this mRNA selectively elicits helper T-cell responses across a range of epitopes and MHC-II alleles. These CD4 T cells show robust, polyfunctional Th1 cytokine release when evaluated ex vivo. We tested the activity of these CD4 T cells in 2 disease models: Salmonella enterica and influenza virus. In both models, these monospecific CD4 T cells influenced the course of infection, demonstrating the utility of this experimental tool, which can produce a monospecific CD4 T-cell response.
Authors
- Michael J. Hogan (ORCID: https://orcid.org/0000-0002-6244-2993)
- Kathleen S Krauss (ORCID: https://orcid.org/0000-0001-9432-6623)
- Stephen D. Carro (ORCID: https://orcid.org/0000-0003-3756-1429)
- Laurence C. Eisenlohr (ORCID: https://orcid.org/0000-0002-8475-7910)
Institutions
- Children's Hospital of Philadelphia (US)
- University of Pennsylvania (US)
Publication Details
- Journal
- The Journal of Immunology
- Published
- 2025-12-02
- DOI
- https://doi.org/10.1093/jimmun/vkaf318
- Citations
- 1
- Primary Topic
- Immunotherapy and Immune Responses
- Type
- article
- Field-Weighted Citation Impact
- 0.80