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Cross-competition shapes CD8+ T cell hierarchies and differentiation after RNA vaccination

Delamarre, L.; Mccarron, M.; Hornburg, M.; Wu, T. D.; Tong, A.-J.; Gutierrez, A.; Tahtinen, S.; Darwish, M.; Freund, E.; Feng, Y.; Eisel, D.; Balanca, C.-C.; Doron, I.; Lan, H.; Lehar, S.; Jones, T. N.; Oei, Y.; Javinal, V.; Navarro, A.; Chestnut, Y.; Wichner, S.; de la Cruz, C.; Haley, B.; Blanchette, C.; Vormehr, M.; Kranz, L.; Sahin, U.; Mellman, i.; Schartner, J.

2025-10-27 immunology
10.1101/2025.10.26.684631 bioRxiv
Show abstract

Short SummaryImmunodominance is a universal feature of adaptive immunity that constrains T cell expansion, clonal diversity and breadth resulting in a narrowly focused T cell response. While observed across diverse priming settings and vaccine platforms, the influence of immunodominance on T cell phenotype remains unclear. Using an mRNA lipoplex vaccine encoding multiple antigens to study how immunodominance influences CD8+ T cell fate, we found that dominant CD8+ T cell responses alter the magnitude and phenotype of subdominant responses through peptide-MHC-I stability-mediated T cell cross-competition. Dominant CD8+ T cell responses preferentially acquired markers associated with terminal differentiation and cytotoxic function, while sub-dominant responses adopted memory-precursor and stem-like features. Removal of dominant responses allowed increased expansion of sub-dominant T cell responses and adoption of terminally differentiated effector phenotypes. These findings reveal that immunodominance dynamically shapes the magnitude, breadth and differentiation of CD8+ T cell responses and highlights opportunities to fine-tune T cell responses for therapeutic vaccination.

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