Inactivated tick-borne encephalitis vaccine elicits several overlapping waves of T cell response
The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generatio...
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| Vydáno v: | Frontiers in immunology Ročník 13; s. 970285 |
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| Jazyk: | angličtina |
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Frontiers Media S.A
24.08.2022
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| ISSN: | 1664-3224, 1664-3224 |
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| Abstract | The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4
+
and CD8
+
T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4
+
and CD8
+
vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes. |
|---|---|
| AbstractList | The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4
+
and CD8
+
T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4
+
and CD8
+
vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes. The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4+ and CD8+ T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4+ and CD8+ vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes. The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4 and CD8 T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4 and CD8 vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes. The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4+ and CD8+ T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4+ and CD8+ vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes.The development and implementation of vaccines have been growing exponentially, remaining one of the major successes of healthcare over the last century. Nowadays, active regular immunizations prevent epidemics of many viral diseases, including tick-borne encephalitis (TBE). Along with the generation of virus-specific antibodies, a highly effective vaccine should induce T cell responses providing long-term immune defense. In this study, we performed longitudinal high-throughput T cell receptor (TCR) sequencing to characterize changes in individual T cell repertoires of 11 donors immunized with an inactivated TBE vaccine. After two-step immunization, we found significant clonal expansion of both CD4+ and CD8+ T cells, ranging from 302 to 1706 vaccine-associated TCRβ clonotypes in different donors. We detected several waves of T cell clonal expansion generated by distinct groups of vaccine-responding clones. Both CD4+ and CD8+ vaccine-responding T cell clones formed 17 motifs in TCRβ sequences shared by donors with identical HLA alleles. Our results indicate that TBE vaccination leads to a robust T cell response due to the production of a variety of T cell clones with a memory phenotype, which recognize a large set of epitopes. |
| Author | Salnikova, Maria A. Komech, Ekaterina A. Vorovitch, Mikhail F. Komkov, Alexander Y. Mamedov, Ilgar Z. Sycheva, Anastasiia L. Pogorelyy, Mikhail V. Kopantzev, Eugene P. Urazbakhtin, Shamil Z. Zvyagin, Ivan V. Lebedev, Yuri B. Minervina, Anastasia A. |
| AuthorAffiliation | 2 Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University , Moscow , Russia 1 Department of Genomics of Adaptive Immunity, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS , Moscow , Russia 4 Computational Systems Biochemistry Research Group, Max Planck Institute of Biochemistry , Martinsried , Germany 3 Department of Immunology, St. Jude Children’s Research Hospital , Memphis, TN , United States 9 Laboratory of Cytogenetics and Molecular Genetics, Dmitry Rogachev National Medical and Research Centre of Paediatric Haematology, Oncology and Immunology , Moscow , Russia 7 Department of Organization and Technology of Production of Immune-and-Biological Products, Institute for Translational Medicine and Biotechnology, Sechenov First Moscow State Medical University , Moscow , Russia 6 Laboratory of Tick-Borne Encephalitis and Other Encephalitis, Chumakov Federal Scientific Center for Research and Development of Imm |
| AuthorAffiliation_xml | – name: 2 Department of Molecular Technologies, Institute of Translational Medicine, Pirogov Russian National Research Medical University , Moscow , Russia – name: 6 Laboratory of Tick-Borne Encephalitis and Other Encephalitis, Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products of RAS (FSASI “Chumakov FSC R&D IBP RAS”) , Moscow , Russia – name: 5 Department of Immunology, Faculty of Biology, Lomonosov Moscow State University , Moscow , Russia – name: 1 Department of Genomics of Adaptive Immunity, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS , Moscow , Russia – name: 7 Department of Organization and Technology of Production of Immune-and-Biological Products, Institute for Translational Medicine and Biotechnology, Sechenov First Moscow State Medical University , Moscow , Russia – name: 4 Computational Systems Biochemistry Research Group, Max Planck Institute of Biochemistry , Martinsried , Germany – name: 8 Department of Genomics and Postgenomic Technologies, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS , Moscow , Russia – name: 3 Department of Immunology, St. Jude Children’s Research Hospital , Memphis, TN , United States – name: 9 Laboratory of Cytogenetics and Molecular Genetics, Dmitry Rogachev National Medical and Research Centre of Paediatric Haematology, Oncology and Immunology , Moscow , Russia |
| Author_xml | – sequence: 1 givenname: Anastasiia L. surname: Sycheva fullname: Sycheva, Anastasiia L. – sequence: 2 givenname: Ekaterina A. surname: Komech fullname: Komech, Ekaterina A. – sequence: 3 givenname: Mikhail V. surname: Pogorelyy fullname: Pogorelyy, Mikhail V. – sequence: 4 givenname: Anastasia A. surname: Minervina fullname: Minervina, Anastasia A. – sequence: 5 givenname: Shamil Z. surname: Urazbakhtin fullname: Urazbakhtin, Shamil Z. – sequence: 6 givenname: Maria A. surname: Salnikova fullname: Salnikova, Maria A. – sequence: 7 givenname: Mikhail F. surname: Vorovitch fullname: Vorovitch, Mikhail F. – sequence: 8 givenname: Eugene P. surname: Kopantzev fullname: Kopantzev, Eugene P. – sequence: 9 givenname: Ivan V. surname: Zvyagin fullname: Zvyagin, Ivan V. – sequence: 10 givenname: Alexander Y. surname: Komkov fullname: Komkov, Alexander Y. – sequence: 11 givenname: Ilgar Z. surname: Mamedov fullname: Mamedov, Ilgar Z. – sequence: 12 givenname: Yuri B. surname: Lebedev fullname: Lebedev, Yuri B. |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36091004$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_3389_fimmu_2023_1245175 crossref_primary_10_3389_fimmu_2024_1352720 crossref_primary_10_1002_eji_70027 crossref_primary_10_3389_fimmu_2023_1182963 crossref_primary_10_7554_eLife_69157 crossref_primary_10_3390_v15040958 |
| Cites_doi | 10.3389/fimmu.2019.02159 10.1016/j.vaccine.2015.12.057 10.1089/088282403322396190 10.1093/nar/gkx760 10.1371/journal.pcbi.1006874 10.1371/journal.pbio.3000314 10.1002/eji.201343751 10.1093/bioinformatics/btz035 10.1073/pnas.1402981111 10.1016/j.vaccine.2018.02.027 10.1038/leu.2016.321 10.1111/bjh.16230 10.1371/journal.pone.0140545 10.1038/s41590-020-0791-5 10.1038/nature22976 10.1073/pnas.1812800116 10.3390/ijms23031029 10.4049/jimmunol.1901115 10.1128/JVI.03474-14 10.3390/vaccines8030451 10.3389/fphys.2018.00879 10.1038/nature22383 10.1016/j.antiviral.2019.01.014 10.1038/s41590-020-00815-y 10.1371/journal.ppat.1004622 10.1126/scitranslmed.aaf1725 10.1093/bioinformatics/btp616 10.4049/immunohorizons.1800029 10.1080/21645515.2019.1600987 10.1073/pnas.1809642115 10.1128/JVI.79.24.15107-15113.2005 10.4049/jimmunol.1300161 10.1126/science.1178334 10.1126/scitranslmed.abj7211 10.1016/j.cell.2021.12.026 10.1128/CVI.00131-10 10.1371/journal.pcbi.1005572 10.1038/nmeth.3364 10.3389/fimmu.2018.02874 10.1017/S1431927621000921 10.1128/JVI.00196-14 10.3389/fimmu.2013.00456 10.7554/eLife.53704 10.1093/infdis/133.1.91 10.1038/s41422-020-0379-5 10.1007/978-1-4614-0980-9_12 10.1038/nri2580 |
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| Copyright | Copyright © 2022 Sycheva, Komech, Pogorelyy, Minervina, Urazbakhtin, Salnikova, Vorovitch, Kopantzev, Zvyagin, Komkov, Mamedov and Lebedev. Copyright © 2022 Sycheva, Komech, Pogorelyy, Minervina, Urazbakhtin, Salnikova, Vorovitch, Kopantzev, Zvyagin, Komkov, Mamedov and Lebedev 2022 Sycheva, Komech, Pogorelyy, Minervina, Urazbakhtin, Salnikova, Vorovitch, Kopantzev, Zvyagin, Komkov, Mamedov and Lebedev |
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| Keywords | TBE vaccination tick-borne encephalitis TCR motif T cell immune response immunological memory clonal expansion TCR repertoire |
| Language | English |
| License | Copyright © 2022 Sycheva, Komech, Pogorelyy, Minervina, Urazbakhtin, Salnikova, Vorovitch, Kopantzev, Zvyagin, Komkov, Mamedov and Lebedev. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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| References | Hopf (B36) 2016; 34 Mamedov (B19) 2013; 4 Robinson (B24) 2010; 26 Miyasaka (B12) 2019; 15 Kubinski (B17) 2020; 8 Mahnke (B38) 2013; 43 Chu (B44) 2020; 21 O’Shea (B32) 2010; 327 Shugay (B27) 2018; 46 Mudd (B15) 2022; 185 Dash (B31) 2017; 547 Choi (B5) 2012 Aberle (B29) 2015; 10 Komkov (B22) 2020; 188 Mayer (B39) 2019; 116 Pogorelyy (B28) 2019; 10 Galletti (B43) 2020; 21 Blom (B46) 2015; 11 Varnaitė (B33) 2020; 204 Schwaiger (B45) 2014; 88 Minervina (B10) 2020; 9 Sethna (B26) 2019; 35 Sycheva (B11) 2018; 36 Gomez (B34) 2003; 16 Ho (B37) 2018; 9 Dupic (B6) 2019; 15 Swanson (B13) 2021; 13 Bortnick (B4) 2013; 190 Zvyagin (B20) 2017; 31 Plotkin Stanley (B2) 2010; 17 Pogorelyy (B9) 2018; 115 Bolotin (B23) 2015; 12 Pogorelyy (B21) 2017; 13 Bunse (B14) 2022; 23 Rappuoli (B1) 2014; 111 Ruzek (B16) 2019; 164 Lampen (B47) 2018; 2 Qi (B8) 2016; 8 Aberle (B35) 2005; 79 Pogorelyy (B25) 2019; 17 DeWitt (B7) 2015; 89 Sullivan (B3) 1976; 133 Barberis (B41) 2018; 9 Glanville (B30) 2017; 547 Moiseenko (B18) 2021; 27 Rochman (B40) 2009; 9 Shyer (B42) 2020; 30 |
| References_xml | – volume: 10 year: 2019 ident: B28 article-title: A framework for annotation of antigen specificities in high-throughput T-cell repertoire sequencing studies publication-title: Front Immunol doi: 10.3389/fimmu.2019.02159 – volume: 34 year: 2016 ident: B36 article-title: Comparable immune responsiveness but increased reactogenicity after subcutaneous versus intramuscular administration of tick borne encephalitis (TBE) vaccine publication-title: Vaccine doi: 10.1016/j.vaccine.2015.12.057 – volume: 16 year: 2003 ident: B34 article-title: Characterization of tick-borne encephalitis virus-specific human T lymphocyte responses by stimulation with structural TBEV proteins expressed in a recombinant baculovirus publication-title: Viral Immunol doi: 10.1089/088282403322396190 – volume: 46 year: 2018 ident: B27 article-title: VDJdb: a curated database of T-cell receptor sequences with known antigen specificity publication-title: Nucleic Acids Res doi: 10.1093/nar/gkx760 – volume: 15 year: 2019 ident: B6 article-title: Genesis of the αβ T-cell receptor publication-title: PloS Comput Biol doi: 10.1371/journal.pcbi.1006874 – volume: 17 year: 2019 ident: B25 article-title: Detecting T cell receptors involved in immune responses from single repertoire snapshots publication-title: PloS Biol doi: 10.1371/journal.pbio.3000314 – volume: 43 year: 2013 ident: B38 article-title: The who’s who of T-cell differentiation: human memory T-cell subsets publication-title: Eur J Immunol doi: 10.1002/eji.201343751 – volume: 35 year: 2019 ident: B26 article-title: OLGA: fast computation of generation probabilities of b- and T-cell receptor amino acid sequences and motifs publication-title: Bioinformatics doi: 10.1093/bioinformatics/btz035 – volume: 111 year: 2014 ident: B1 article-title: Vaccines, new opportunities for a new society publication-title: Proc Natl Acad Sci U.S.A. doi: 10.1073/pnas.1402981111 – volume: 36 year: 2018 ident: B11 article-title: Quantitative profiling reveals minor changes of T cell receptor repertoire in response to subunit inactivated influenza vaccine publication-title: Vaccine doi: 10.1016/j.vaccine.2018.02.027 – volume: 31 year: 2017 ident: B20 article-title: Tracking T-cell immune reconstitution after TCRαβ/CD19-depleted hematopoietic cells transplantation in children publication-title: Leukemia doi: 10.1038/leu.2016.321 – volume: 188 year: 2020 ident: B22 article-title: High-throughput sequencing of T-cell receptor alpha chain clonal rearrangements at the DNA level in lymphoid malignancies publication-title: Br J Haematol doi: 10.1111/bjh.16230 – volume: 10 year: 2015 ident: B29 article-title: Human CD4+ T helper cell responses after tick-borne encephalitis vaccination and infection publication-title: PloS One doi: 10.1371/journal.pone.0140545 – volume: 21 year: 2020 ident: B43 article-title: Two subsets of stem-like CD8+ memory T cell progenitors with distinct fate commitments in humans publication-title: Nat Immunol doi: 10.1038/s41590-020-0791-5 – volume: 547 year: 2017 ident: B30 article-title: Identifying specificity groups in the T cell receptor repertoire publication-title: Nature doi: 10.1038/nature22976 – volume: 116 year: 2019 ident: B39 article-title: Regulation of T cell expansion by antigen presentation dynamics publication-title: Proc Natl Acad Sci U.S.A. doi: 10.1073/pnas.1812800116 – volume: 23 start-page: 1029 year: 2022 ident: B14 article-title: Common T-Cell-Receptor motifs and features in patients with cytomegalovirus (CMV)-seronegative end-stage renal disease receiving a peptide vaccination against CMV publication-title: Int J Mol Sci doi: 10.3390/ijms23031029 – volume: 204 year: 2020 ident: B33 article-title: Magnitude and functional profile of the human CD4+ T cell response throughout primary immunization with tick-borne encephalitis virus vaccine publication-title: J Immunol doi: 10.4049/jimmunol.1901115 – volume: 89 year: 2015 ident: B7 article-title: Dynamics of the cytotoxic T cell response to a model of acute viral infection publication-title: J Virol doi: 10.1128/JVI.03474-14 – volume: 8 start-page: 451 year: 2020 ident: B17 article-title: Tick-borne encephalitis virus: A quest for better vaccines against a virus on the rise publication-title: Vaccines (Basel) doi: 10.3390/vaccines8030451 – volume: 9 year: 2018 ident: B41 article-title: Simulation of stimulation: Cytokine dosage and cell cycle crosstalk driving timing-dependent T cell differentiation publication-title: Front Physiol doi: 10.3389/fphys.2018.00879 – volume: 547 start-page: 89 year: 2017 ident: B31 article-title: Quantifiable predictive features define epitope-specific T cell receptor repertoires publication-title: Nature doi: 10.1038/nature22383 – volume: 164 start-page: 23 year: 2019 ident: B16 article-title: Tick-borne encephalitis in Europe and Russia: Review of pathogenesis, clinical features, therapy, and vaccines publication-title: Antiviral Res doi: 10.1016/j.antiviral.2019.01.014 – volume: 21 year: 2020 ident: B44 article-title: Two parallel worlds of memory T cells publication-title: Nat Immunol doi: 10.1038/s41590-020-00815-y – volume: 11 year: 2015 ident: B46 article-title: Specificity and dynamics of effector and memory CD8 T cell responses in human tick-borne encephalitis virus infection publication-title: PloS Pathog doi: 10.1371/journal.ppat.1004622 – volume: 8 start-page: 332ra46 year: 2016 ident: B8 article-title: Diversification of the antigen-specific T cell receptor repertoire after varicella zoster vaccination publication-title: Sci Transl Med doi: 10.1126/scitranslmed.aaf1725 – volume: 26 year: 2010 ident: B24 article-title: edgeR: a bioconductor package for differential expression analysis of digital gene expression data publication-title: Bioinformatics doi: 10.1093/bioinformatics/btp616 – volume: 2 year: 2018 ident: B47 article-title: Breadth and dynamics of HLA-A2– and HLA-B7–restricted CD8+ T cell responses against nonstructural viral proteins in acute human tick-borne encephalitis virus infection publication-title: ImmunoHorizons doi: 10.4049/immunohorizons.1800029 – volume: 15 year: 2019 ident: B12 article-title: Next-generation sequencing analysis of the human T-cell and b-cell receptor repertoire diversity before and after hepatitis b vaccination publication-title: Hum Vaccin Immunother doi: 10.1080/21645515.2019.1600987 – volume: 115 year: 2018 ident: B9 article-title: Precise tracking of vaccine-responding T cell clones reveals convergent and personalized response in identical twins publication-title: Proc Natl Acad Sci U.S.A. doi: 10.1073/pnas.1809642115 – volume: 79 year: 2005 ident: B35 article-title: Humoral and cellular immune response to RNA immunization with flavivirus replicons derived from tick-borne encephalitis virus publication-title: J Virol doi: 10.1128/JVI.79.24.15107-15113.2005 – volume: 190 year: 2013 ident: B4 article-title: What is and what should always have been: long-lived plasma cells induced by T cell-independent antigens publication-title: J Immunol doi: 10.4049/jimmunol.1300161 – volume: 327 year: 2010 ident: B32 article-title: Mechanisms underlying lineage commitment and plasticity of helper CD4+ T cells publication-title: Science doi: 10.1126/science.1178334 – volume: 13 year: 2021 ident: B13 article-title: AZD1222/ChAdOx1 nCoV-19 vaccination induces a polyfunctional spike protein-specific TH1 response with a diverse TCR repertoire publication-title: Sci Transl Med doi: 10.1126/scitranslmed.abj7211 – volume: 185 start-page: 603 year: 2022 ident: B15 article-title: SARS-CoV-2 mRNA vaccination elicits a robust and persistent T follicular helper cell response in humans publication-title: Cell doi: 10.1016/j.cell.2021.12.026 – volume: 17 year: 2010 ident: B2 article-title: Correlates of protection induced by vaccination publication-title: Clin Vaccine Immunol doi: 10.1128/CVI.00131-10 – volume: 13 year: 2017 ident: B21 article-title: Persisting fetal clonotypes influence the structure and overlap of adult human T cell receptor repertoires publication-title: PloS Comput Biol doi: 10.1371/journal.pcbi.1005572 – volume: 12 year: 2015 ident: B23 article-title: MiXCR: software for comprehensive adaptive immunity profiling publication-title: Nat Methods doi: 10.1038/nmeth.3364 – volume: 9 year: 2018 ident: B37 article-title: Adjuvants enhancing cross-presentation by dendritic cells: The key to more effective vaccines publication-title: Front Immunol doi: 10.3389/fimmu.2018.02874 – volume: 27 year: 2021 ident: B18 article-title: Estimation of the structural heterogeneity of tick-borne encephalitis vaccine particles publication-title: Microsc Microanal doi: 10.1017/S1431927621000921 – volume: 88 year: 2014 ident: B45 article-title: Specificities of human CD4+ T cell responses to an inactivated flavivirus vaccine and infection: correlation with structure and epitope prediction publication-title: J Virol doi: 10.1128/JVI.00196-14 – volume: 4 year: 2013 ident: B19 article-title: Preparing unbiased T-cell receptor and antibody cDNA libraries for the deep next generation sequencing profiling publication-title: Front Immunol doi: 10.3389/fimmu.2013.00456 – volume: 9 start-page: e53704 year: 2020 ident: B10 article-title: Primary and secondary anti-viral response captured by the dynamics and phenotype of individual T cell clones publication-title: Elife doi: 10.7554/eLife.53704 – volume: 133 year: 1976 ident: B3 article-title: Influenza virus infection in nude mice publication-title: J Infect Dis doi: 10.1093/infdis/133.1.91 – volume: 30 year: 2020 ident: B42 article-title: Metabolic signaling in T cells publication-title: Cell Res doi: 10.1038/s41422-020-0379-5 – start-page: 267 volume-title: Viral molecular machines year: 2012 ident: B5 article-title: Viral polymerases doi: 10.1007/978-1-4614-0980-9_12 – volume: 9 year: 2009 ident: B40 article-title: New insights into the regulation of T cells by gamma(c) family cytokines publication-title: Nat Rev Immunol doi: 10.1038/nri2580 |
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| SubjectTerms | Antibodies, Viral CD8-Positive T-Lymphocytes clonal expansion Encephalitis Viruses, Tick-Borne Encephalitis, Tick-Borne - prevention & control Humans immunological memory Immunology T cell immune response TBE vaccination TCR motif TCR repertoire Viral Vaccines |
| Title | Inactivated tick-borne encephalitis vaccine elicits several overlapping waves of T cell response |
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