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The T cell receptor repertoire reflects the dynamics of the immune response to vaccination
Kevin Mohammed; Austin Meadows; Sandra Hatem; Saboor Hekmaty; Viviana Simon; Anitha D Jayaprakash; Ravi Sachidanandam.
Affiliation
  • Kevin Mohammed; Icahn School of Medicine at Mount Sinai, NY 10029
  • Austin Meadows; Girihlet Inc., 355 30th St., Oakland, CA 94609
  • Sandra Hatem; Icahn School of Medicine at Mount Sinai, NY 10029
  • Saboor Hekmaty; Icahn School of Medicine at Mount Sinai
  • Viviana Simon; Icahn School of Medicine at Mount Sinai, NY 10029
  • Anitha D Jayaprakash; Girihlet Inc., 355 30th St, Oakland, CA 94609
  • Ravi Sachidanandam; Icahn School of Medicine at Mount Sinai
Preprint in English | bioRxiv | ID: ppbiorxiv-471735
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.
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies Language: English Year: 2021 Document type: Preprint
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