Статья

CD4+ T Follicular Helper Cells in Human Tonsils and Blood Are Clonally Convergent but Divergent from Non-Tfh CD4+ Cells

E. Brenna, A. Davydov, K. Ladell, J. McLaren, P. Bonaiuti, M. Metsger, J. Ramsden, S. Gilbert, T. Lambe, D. Price, S. Campion, D. Chudakov, P. Borrow, A. McMichael,
2021

T follicular helper (Tfh) cells are fundamental for B cell selection and antibody maturation in germinal centers. Circulating Tfh (cTfh) cells constitute a minor proportion of the CD4+ T cells in peripheral blood, but their clonotypic relationship to Tfh populations resident in lymph nodes and the extent to which they differ from non-Tfh CD4+ cells have been unclear. Using donor-matched blood and tonsil samples, we investigate T cell receptor (TCR) sharing between tonsillar Tfh cells and peripheral Tfh and non-Tfh cell populations. TCR transcript sequencing reveals considerable clonal overlap between peripheral and tonsillar Tfh cell subsets as well as a clear distinction between Tfh and non-Tfh cells. Furthermore, influenza-specific cTfh cell clones derived from blood can be found in the repertoire of tonsillar Tfh cells. Therefore, human blood samples can be used to gain insight into the specificity of Tfh responses occurring in lymphoid tissues, provided that cTfh subsets are studied. © 2019 The AuthorsCD4+ T follicular helper (Tfh) cells are fundamental for antibody production. Brenna et al. demonstrate extensive repertoire overlap between Tfh populations in human blood and tonsils, whereas non-Tfh repertoires differ profoundly. Therefore, analysis of Tfh but not of total circulating CD4+ T cells can reflect the specificity of lymphoid tissue Tfh cells. © 2019 The Authors

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  • 1. Version of Record от 2021-04-27

Метаданные

Об авторах
  • E. Brenna
    Nuffield Department of Clinical Medicine, University of Oxford, Oxford, OX3 7FZ, United Kingdom
  • A. Davydov
    Central European Institute of Technology, Brno, 601 77, Czech Republic
  • K. Ladell
    Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, United Kingdom
  • J. McLaren
    Istituto Firc di Oncologia Molecolare, Milano, 20139, Italy
  • P. Bonaiuti
    West Wing ENT, John Radcliffe Hospital, Oxford, OX3 9DU, United Kingdom
  • M. Metsger
    The Jenner Institute, University of Oxford, Oxford, OX3 7DQ, United Kingdom
  • J. Ramsden
    Systems Immunity Research Institute, Cardiff University School of Medicine, Cardiff, CF14 4XN, United Kingdom
  • S. Gilbert
    Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, Moscow, 117997, Russian Federation
  • T. Lambe
    Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, Moscow, 117997, Russian Federation
  • D. Price
  • S. Campion
  • D. Chudakov
  • P. Borrow
  • A. McMichael
Название журнала
  • Cell Reports
Том
  • 30
Выпуск
  • 1
Страницы
  • 137-152.e5
Ключевые слова
  • chemokine receptor CXCR3; Influenza virus hemagglutinin; adolescent; adult; CD4+ T lymphocyte; cell clone; cell size; computer simulation; cytology; donor; human; immunology; lymphocyte subpopulation; metabolism; middle aged; palatine tonsil; Tfh cell; young adult; Adolescent; Adult; CD4-Positive T-Lymphocytes; Cell Size; Clone Cells; Computer Simulation; Hemagglutinin Glycoproteins, Influenza Virus; Humans; Lymphocyte Subsets; Middle Aged; Palatine Tonsil; Receptors, CXCR3; T Follicular Helper Cells; Tissue Donors; Young Adult
Издатель
  • Elsevier B.V.
Тип документа
  • journal article
Тип лицензии Creative Commons
  • CC
Правовой статус документа
  • Свободная лицензия
Источник
  • scopus