bioRxivImmunologyPreprint
Cross-competition shapes CD8+ T cell hierarchies and differentiation after RNA vaccination
Mark J. McCarroniD, Milena Hornburg, Thomas D. WuiD, Ann-Jay TongiD, Siri TähtineniD, Martine DarwishiD, Emily C. FreundiD, Ying FengiD, David EiseliD, Camille-Charlotte BalançaiD, Itai Doron, Huan Lan, Sophie M. Lehar, Tamaki Nozawa, Yoko A. Oei, Vincent Javinal, Armando Navarro, Yajun Chestnut, Alan Gutierrez, Sara M. WichneriD, Cecile de la Cruz, Benjamin HaleyiD, Craig BlanchetteiD, Mathias VormehriD, Lena M. KranziD, , Lélia DelamarreiD
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.
- organism: human
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: cell signaling & trafficking
- approach: experimental assay
- Citations
- 5
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