The T cell receptor repertoire reflects the dynamics of the immune response to vaccination
K. Mohammed, A. Meadows, S. Hatem, S. Hekmaty, V. Simon, A. D. Jayaprakash, R. Sachidanandam
Abstract
Early, high-resolution metrics are needed to ascertain the immune response to vaccinations. The T cell receptor (TCR), a heterodimer of one and one {beta} chain, is a promising target, with the complete TCR repertoire reflecting the T cells present in an individual. To this end, we developed Tseek, an unbiased and accurate method for profiling the TCR repertoire by sequencing the TCR and {beta} chains and developing a suite of tools for repertoire analysis. An added advantage is the ability to non-invasively analyze T cells in peripheral blood mononuclear cells (PBMCs). Tseek and the analytical suite were used to explore the T cell response to both the COVID-19 mRNA vaccine (n=9) and the seasonal inactivated Influenza vaccine (n=5) at several time points. Neutralizing antibody titers were also measured in the covid vaccine samples. The COVID-19 vaccine elicited a broad T cell response involving multiple expanded clones, whereas the Influenza vaccine elicited a narrower response involving fewer clones. Many distinct T cell clones responded at each time point, over a month, providing temporal details lacking in the antibody measurements, especially before the antibodies are detectable. In individuals recovered from a SARS-CoV-2 infection, the first vaccine dose elicited a robust T cell response, while the second dose elicited a comparatively weaker response, indicating a saturation of the response. The physical symptoms experienced by the recipients immediately following the vaccinations were not indicative of the TCR/antibody responses. The TCR responses broadly presaged the antibody responses. We also found that the TCR repertoire acts as an individual fingerprint: donors of blood samples taken years apart could be identified solely based upon their TCR repertoire, hinting at other surprising uses the TCR repertoire may have. These results demonstrate the promise of TCR repertoire sequencing as an early and sensitive measure of the adaptive immune response to vaccination, which can help improve immunogen selection and optimize vaccine dosage and spacing between doses.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Contrasting Effects of SARS-CoV-2 Vaccination vs. Infection on Antibody and TCR Repertoires
J. Braun, E. D. Hill, … R. Arnaout·bioRxiv·Sep 8, 2023
- Longitudinal high-throughput TCR repertoire profiling reveals the dynamics of T cell memory formation after mild COVID-19 infection
A. A. Minervina, E. A. Komech, … M. V. Pogorelyy·bioRxiv·May 18, 2020
- Single cell profiling of T and B cell repertoires following SARS-CoV-2 mRNA vaccine
S. Sureshchandra, S. A. Lewis, … I. Messaoudi·bioRxiv·Jul 14, 2021
- Association between COVID-19 Disease Severity and T Cell Receptor Repertoire
Xinyi Chen, Yapeng Su, … Wei Sun·bioRxiv·Nov 26, 2024
- Quality of vaccination-induced T cell responses is conveyed by polyclonality and high, but not maximum, antigen receptor avidity
Katharina Kocher, Felix Drost, … Kilian Schober·Science ImmunologyPeer-reviewed·Oct 3, 2025
- Precise tracking of vaccine-responding T-cell clones reveals convergent and personalized response in identical twins
M. V. Pogorelyy, A. A. Minervina, … Y. B. Lebedev·bioRxiv·Apr 13, 2018