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Dynamic regulation of TFH selection during the germinal centre reaction

Author

Listed:
  • Julia Merkenschlager

    (The Rockefeller University)

  • Shlomo Finkin

    (The Rockefeller University)

  • Victor Ramos

    (The Rockefeller University)

  • Julian Kraft

    (The Rockefeller University)

  • Melissa Cipolla

    (The Rockefeller University)

  • Carla R. Nowosad

    (The Rockefeller University)

  • Harald Hartweger

    (The Rockefeller University)

  • Wenzhu Zhang

    (The Rockefeller University)

  • Paul Dominic B. Olinares

    (The Rockefeller University)

  • Anna Gazumyan

    (The Rockefeller University
    The Rockefeller University)

  • Thiago Y. Oliveira

    (The Rockefeller University)

  • Brian T. Chait

    (The Rockefeller University)

  • Michel C. Nussenzweig

    (The Rockefeller University
    The Rockefeller University)

Abstract

The germinal centre is a dynamic microenvironment in which B cells that express high-affinity antibody variants produced by somatic hypermutation are selected for clonal expansion by limiting the numbers of T follicular helper cells1,2. Although much is known about the mechanisms that control the selection of B cells in the germinal centre, far less is understood about the clonal behaviour of the T follicular helper cells that help to regulate this process. Here we report on the dynamic behaviour of T follicular helper cell clones during the germinal centre reaction. We find that, similar to germinal centre B cells, T follicular helper cells undergo antigen-dependent selection throughout the germinal centre reaction that results in differential proliferative expansion and contraction. Increasing the amount of antigen presented in the germinal centre leads to increased division of T follicular helper cells. Competition between T follicular helper cell clones is mediated by the affinity of T cell receptors for peptide–major-histocompatibility-complex ligands. T cells that preferentially expand in the germinal centre show increased expression of genes downstream of the T cell receptor, such as those required for metabolic reprogramming, cell division and cytokine production. These dynamic changes lead to marked remodelling of the functional T follicular helper cell repertoire during the germinal centre reaction.

Suggested Citation

  • Julia Merkenschlager & Shlomo Finkin & Victor Ramos & Julian Kraft & Melissa Cipolla & Carla R. Nowosad & Harald Hartweger & Wenzhu Zhang & Paul Dominic B. Olinares & Anna Gazumyan & Thiago Y. Oliveir, 2021. "Dynamic regulation of TFH selection during the germinal centre reaction," Nature, Nature, vol. 591(7850), pages 458-463, March.
  • Handle: RePEc:nat:nature:v:591:y:2021:i:7850:d:10.1038_s41586-021-03187-x
    DOI: 10.1038/s41586-021-03187-x
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    Cited by:

    1. Bonnie Huang & James D. Phelan & Silvia Preite & Julio Gomez-Rodriguez & Kristoffer H. Johansen & Hirofumi Shibata & Arthur L. Shaffer & Qin Xu & Brendan Jeffrey & Martha Kirby & Stacie Anderson & Yan, 2022. "In vivo CRISPR screens reveal a HIF-1α-mTOR-network regulates T follicular helper versus Th1 cells," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Julia Merkenschlager & Riza-Maria Berz & Victor Ramos & Maximilian Uhlig & Andrew J. MacLean & Carla R. Nowosad & Thiago Y. Oliveira & Michel C. Nussenzweig, 2023. "Continually recruited naïve T cells contribute to the follicular helper and regulatory T cell pools in germinal centers," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

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