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.

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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
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article

An mRNA platform to create isolated, monospecific Th1 responses

Michael J. Hogan, Kathleen S Krauss, Stephen D. Carro, Laurence C. Eisenlohr
1 citations
The Journal of Immunology
Immunotherapy and Immune Responses
0.80
article

An mRNA platform to create isolated, monospecific Th1 responses

Michael J. Hogan, Kathleen S Krauss, Stephen D. Carro, Laurence C. Eisenlohr
article en
1 citations

Abstract

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.

The Journal of ImmunologyVol. 215(2)
Children's Hospital of Philadelphia (US), University of Pennsylvania (US)
Openalex Percentile: Top 21%
Immunotherapy and Immune Responses
0.80
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