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T Cell Responses Induced by SARS-CoV-2 mRNA Vaccination Are Associated With Clonal Replacement

60 Pages Posted: 18 Oct 2022 Publication Status: Review Complete

See all articles by Hiroyasu Aoki

Hiroyasu Aoki

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases

Masahiro Kitabatake

Nara Medical University - Department of Immunology

Haruka Abe

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases

Shigeyuki Shichino

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases

Atsushi Hara

Nara Medical University - Department of Immunology

Noriko Ouji-Sageshima

Nara Medical University - Department of Immunology

Toshihiro Ito

Nara Medical University - Department of Immunology

Kouji Matsushima

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases

Satoshi Ueha

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases

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Abstract

mRNA vaccines against the Spike glycoprotein of severe acute respiratory syndrome type 2 coronavirus (SARS-CoV-2) elicit strong T-cell responses. However, it is unknown whether T cell clones induced by the first vaccination or newly generated T cell clones dominate responses to the secondary vaccination. Here, we analyzed the kinetic profile of Spike-reactive T-cell clones before the first dose, one week after the first and second dose, and four weeks after the second dose of the BNT162b mRNA vaccine. Interestingly, a new set of Spike-reactive CD8 + T cell clones exhibited the greatest expansion following secondary vaccination and replaced the clones that had responded to the primary vaccination. Single-cell mRNA/protein/TCR analysis revealed that the first-responder clones exhibited a terminally differentiated phenotype, whereas second-responder clones exhibited an actively proliferating phenotype. These results show that Spike-reactive T cell responses induced by repetitive mRNA vaccination are augmented and maintained by replacement with newly-generated clones with proliferative potential.

Funding Information: This work was supported by Japan Society for the Promotion of Science (JSPS) under Grant Number 17929397 and 20281832, and Japan Agency for Medical Research and Development (AMED) under Grant Number JP22fk0310509, JP22ama221306, and P21gm6210025.

Declaration of Interests: H.A. reports stock for ImmunoGeneTeqs, Inc. S.S. reports advisory role for ImmunoGeneTeqs, Inc; stock for ImmunoGeneTeqs, Inc, T.I. reports research funding from Rohto Pharmaceutical Co., Ltd. and Biometrics Sympathies Inc. K.M. reports consulting or advisory role for Kyowa-Hakko Kirin, ImmunoGeneTeqs, Inc; research funding from Kyowa-Hakko Kirin, and Ono; stock for ImmunoGeneTeqs, Inc, IDAC Theranostics, Inc. S.U. reports advisory role for ImmunoGeneTeqs, Inc; stock for ImmunoGeneTeqs, Inc, IDAC Theranostics, Inc. M.K., H.A., A.H., and N.O.S. report no conflict of interest to disclose.

Ethics Approval Statement: The Nara Medical University Ethics Committee approved the study (No. 3168). The study was conducted in accordance with the Declaration of Helsinki and Good Clinical Practice Guidelines, following approval by the ethics board in each institution. All study participants provided written informed consent.

Keywords: SARS-CoV-2, mRNA vaccine, CD8 T cells, T cell memory, TCR repertoire, single-cell TCR/RNAseq, Clonal replacement

Suggested Citation

Aoki, Hiroyasu and Kitabatake, Masahiro and Abe, Haruka and Shichino, Shigeyuki and Hara, Atsushi and Ouji-Sageshima, Noriko and Ito, Toshihiro and Matsushima, Kouji and Ueha, Satoshi, T Cell Responses Induced by SARS-CoV-2 mRNA Vaccination Are Associated With Clonal Replacement. Available at SSRN: https://ssrn.com/abstract=4232457 or http://dx.doi.org/10.2139/ssrn.4232457
This version of the paper has not been formally peer reviewed.

Hiroyasu Aoki

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases ( email )

Masahiro Kitabatake

Nara Medical University - Department of Immunology ( email )

Haruka Abe

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases ( email )

Shigeyuki Shichino

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases ( email )

Atsushi Hara

Nara Medical University - Department of Immunology ( email )

Noriko Ouji-Sageshima

Nara Medical University - Department of Immunology ( email )

Toshihiro Ito

Nara Medical University - Department of Immunology ( email )

Kouji Matsushima

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases ( email )

Satoshi Ueha (Contact Author)

Tokyo University of Science - Division of Molecular Regulation of Inflammatory and Immune Diseases ( email )

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