T cell epitope mapping reveals immunodominance of evolutionarily conserved regions within SARS-CoV-2 proteome Journal Article


Authors: Cimen Bozkus, C.; Brown, M.; Velazquez, L.; Thomas, M.; Wilson, E. A.; O'Donnell, T.; Kaminska, A.; Ruchnewitz, D.; Geertz, D.; Bykov, Y.; Kodysh, J.; Oguntuyo, K. Y.; Roudko, V.; Hoyos, D.; Srivastava, K. D.; Kleiner, G.; Alshammary, H.; Karekar, N.; McClain, C.; Gopal, R.; Nie, K.; Del Valle, D.; Delbeau-Zagelbaum, D.; Rodriguez, D.; Setal, J.; The Mount Sinai COVID-19 Biobank Team; Carroll, E.; Wiesendanger, M.; Gulko, P. S.; Charney, A.; Merad, M.; Kim-Schulze, S.; Lee, B.; Wajnberg, A.; Simon, V.; Greenbaum, B. D.; Chowell, D.; Vabret, N.; Luksza, M.; Bhardwaj, N.
Article Title: T cell epitope mapping reveals immunodominance of evolutionarily conserved regions within SARS-CoV-2 proteome
Abstract: Understanding the breadth and functional profile of T cell responses is crucial for assessing their role in immune surveillance of emerging SARS-CoV-2 variants. Sampling healthy individuals, we profiled the kinetics and polyfunctionality of T cell immunity elicited by mRNA vaccination. Modeling of anti-spike T cell responses against ancestral and variant strains suggested epitope immunodominance and cross-reactivity as major predictive determinants of T cell immunity. To identify immunodominant epitopes, we comprehensively mapped CD4+ and CD8+ T cell epitopes within non-spike proteins using samples from convalescent patients. We found that immunodominant epitopes mainly resided within regions that were minimally disrupted by emerging mutations. Conservation analysis across human coronaviruses and in silico alanine scanning highlighted the functional importance of mutationally constrained immunodominant regions. Collectively, these findings identify immunodominant T cell epitopes across the SARS-CoV-2 proteome that may enhance immune surveillance against emerging variants and inform next-generation vaccine designs providing broader and more durable protection. © 2025 The Authors
Keywords: virology; immunology; immunity; microbiology; natural sciences; biological sciences
Journal Title: iScience
Volume: 28
Issue: 8
ISSN: 2589-0042
Publisher: Cell Press  
Date Published: 2025-08-15
Start Page: 113044
Language: English
DOI: 10.1016/j.isci.2025.113044
PROVIDER: scopus
PMCID: PMC12312045
PUBMED: 40746995
DOI/URL:
Notes: Article -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PDF -- Source: Scopus
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  1. David Hoyos
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