Jul 2026· Journal of Immunology· Vol 215· 0 citations
TL;DR
It is demonstrated that the optimal induction of CD8 T-cells requires IFN-I signaling in multiple myeloid cell types, not just in CD8 T-cells, dendritic cells, or monocytes, and that regulation of IFN-β by NF-κB and all IFN-I subtypes by IRF is required to induce protective CD8 T-cells.
Abstract
The modification of RNA by the incorporation of N-methyl pseudo-uridine (N1mψ) renders the mRNA less inflammatory, resulting in durable cellular and humoral responses. Interestingly, mRNA-LNP vaccines still elicit strong innate immune activation and stimulate the production of type I interferons (IFN-I) by antigen-presenting cells (APCs). IFN-I is critical in the induction of CD8 T-cell responses to mRNA vaccines; however, the mechanisms underlying this process are poorly understood.
We determined protection from lethal infection with ectromelia virus in mice with cell-specific deletion of IFNAR1, as well as in mice deficient in specific IFN-I, following vaccination with a previously described EVM158 mRNA-LNP vaccine containing an immunodominant CD8 T-cell epitope.
We demonstrate that the optimal induction of CD8 T-cells requires IFN-I signaling in multiple myeloid cell types, not just in CD8 T-cells, dendritic cells, or monocytes. We also show that at optimal vaccine doses, IFN-β- and IFN-α-deficient mice generate protective CD8 T-cell responses. However, at suboptimal doses, male mice deficient in IFN-β and in IFN-α4, which are regulated by constitutive transcription factors, do not generate completely protective CD8 T cells. Moreover, mice deficient in the NF-κB binding site in the IFN-β promoter and the transcription factor IRF7 generate poorly protective responses.
Our results indicate that optimal induction of protective CD8 T-cell responses by mRNA LNP vaccines requires IFN-I signaling in myeloid cells but not in CD8 T-cells, that IFN-β and IFN-α can individually provide the signals required for protection, and that regulation of IFN-β by NF-κB and all IFN-I subtypes by IRF is required to induce protective CD8 T-cells.
NIAID, NIH
Vaccines and Immunotherapy (VAC)
Tuberculosis (TB) remains the leading cause of death from a single infectious agent worldwide, highlighting the need for improved vaccines beyond the limited protection currently provided by the Bacillus Calmette-Guérin (BCG) vaccine. Here we investigated the immunological impact of incorporating alpha-Galactosylcera...
Ilke Aernout, Thomas Ehouarne, Kevin Mwangi et al.· Frontiers in Immunology· 0 citations
It is demonstrated that PAR-2 activation functions as a potent mucosal adjuvant by enhancing early immune cell recruitment, DC activation, and adaptive T cell responses in lymph nodes, ultimately promoting tissue-resident immunity.
C. Kornuta, Gang Zhou, K. Kane et al.· Vaccine· 0 citations
Dengue virus rNS3pro immunization drives a robust expansion of multifaceted regulatory-like T-cell phenotypes, identifying the NS3 protease domain as a potential player in DENV immune evasion strategies.
V. Romero-Cruz, A. Ramos-Ligonio, Diana Lizzet Murrieta-León et al.· Acta Tropica· 0 citations
Background/Objectives: Systemic administration of recombinant cytokines for immunomodulation in cancer and chronic infection is limited by toxicity and poor spatial control. Messenger RNA (mRNA)-encoded cytokines offer a programmable alternative, but the immunological consequences of interferon-β (IFN-β) mRNA delivery...
Silvia Fraude-El Ghazi, M. Limeres, R. Gambaro et al.· Vaccines· 0 citations
INTRODUCTION.
Despite the effectiveness of existing COVID-19 vaccines, the emergence of new SARS-CoV-2 variants necessitates the development of immunogens capable of eliciting a broad, cross-reactive immune response. A promising approach is the development of mRNA vaccines that induce both humoral and T-cell respons...
M. B. Borgoyakova, A. P. Rudometov, S. V. Sharabrin et al.· Biological Products. Prevent...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.