P-1454. mRNA-Based Respiratory Syncytial Virus Vaccine mRNA-1345 Induces Robust, Polyfunctional, and Durable CD4+ and CD8+ T Cell Responses with Similar Features in Adults Across Age Groups
Yanbo Sun, Emily Marcisak, Daniel Makrinos, Jenna Landy, Shannon McGrath, Hsiaohsuan Kuo, Maria Cavallaro, Christopher Wu, Adam Essene, Haining Lin, Wen-Han Yu, Anthony DiPiazza, Jaap Oostendorp, Robert Paris

TL;DR
An mRNA-based RSV vaccine induces strong and lasting T-cell responses in adults of all ages.
Contribution
The study demonstrates durable and polyfunctional CD4+ and CD8+ T-cell responses to mRNA-1345 across age groups.
Findings
mRNA-1345 induces robust and sustained CD4+ T-cell responses in both younger and older adults.
Vaccination increases CD8+ T-cell frequencies and enhances T-cell polyfunctionality.
Single-cell analysis shows similar T-cell phenotypes and clonal architecture across age groups.
Abstract
Respiratory syncytial virus (RSV) remains a major cause of morbidity and mortality, particularly among infants, the elderly, and individuals with high-risk conditions associated with severe outcomes. While neutralizing antibodies play a key role in protecting against initial infection and limiting viral replication, T cells are increasingly recognized as a critical component of the immune response to mitigate disease severity. Given the age-associated decline in T-cell function, evaluating T-cell responses to the mRNA-based RSV vaccine mRNA-1345 across age groups is important. In this clinical study (NCT05397223), healthy adults 18 to 75 years of age received 1 dose of mRNA-1345 (50 µg). Participant T-cell responses were evaluated by intracellular cytokine staining, activation-induced marker, and Meso Scale Discovery assays at several time points, up to 24 months after vaccination.…
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Taxonomy
TopicsRespiratory viral infections research · Virology and Viral Diseases · Virus-based gene therapy research
