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Early-life thymectomy leads to an increase of granzyme-producing γδ T cells in children with congenital heart disease

Author

Listed:
  • Alexa Cramer

    (Hannover Medical School)

  • Tao Yang

    (Hannover Medical School)

  • Lennart Riemann

    (Hannover Medical School
    Allergology and Neonatology, Hannover Medical School)

  • Vicente Almeida

    (Hannover Medical School)

  • Christoph Kammeyer

    (Hannover Medical School)

  • Yusuf E. Abu

    (Hannover Medical School)

  • Elisa Gluschke

    (Hannover Medical School)

  • Svea Kleiner

    (Hannover Medical School)

  • Ximena León-Lara

    (Hannover Medical School)

  • Anika Janssen

    (Hannover Medical School)

  • Alejandro Hofmann

    (Hannover Medical School)

  • Alexander Horke

    (Transplantation and Vascular Surgery, Hannover Medical School)

  • Constantin Kaisenberg

    (Gynecology and Reproductive Medicine, Hannover Medical School (MHH))

  • Reinhold Förster

    (Hannover Medical School
    Hannover Medical School)

  • Philipp Beerbaum

    (Hannover Medical School)

  • Martin Boehne

    (Hannover Medical School)

  • Sarina Ravens

    (Hannover Medical School
    Hannover Medical School)

Abstract

Congenital heart disease (CHD) is the most common birth defect in newborns, often requiring cardiac surgery with concomitant thymectomy that is known to increase disease susceptibility later in life. Studies of γδ T cells, which are one of the dominant T cells in the early fetal human thymus, are rare. Here, we provide a comprehensive analysis of the γδ T cell compartment via flow cytometry and next-generation sequencing in children and infants with CHD, who underwent cardiac surgery shortly after birth. A perturbation of the γδ T cell repertoire is evident, and Vδ1 T cell numbers are reduced. However, those cells that are present, do retain cytotoxicity. In contrast, GZMA+CD28+CD161hi innate effector Vγ9Vδ2 T cells are found in higher proportions. TCR-seq identifies an increase in TRDJ3+ γδ T cell clones in children with CHD, but not in a confirmatory group of neonates prior to CHD surgery, which overall points to a persistence of fetal-derived effector γδ T cells in children with CHD.

Suggested Citation

  • Alexa Cramer & Tao Yang & Lennart Riemann & Vicente Almeida & Christoph Kammeyer & Yusuf E. Abu & Elisa Gluschke & Svea Kleiner & Ximena León-Lara & Anika Janssen & Alejandro Hofmann & Alexander Horke, 2024. "Early-life thymectomy leads to an increase of granzyme-producing γδ T cells in children with congenital heart disease," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51673-3
    DOI: 10.1038/s41467-024-51673-3
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    References listed on IDEAS

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    1. Mikhail Shugay & Dmitriy V Bagaev & Maria A Turchaninova & Dmitriy A Bolotin & Olga V Britanova & Ekaterina V Putintseva & Mikhail V Pogorelyy & Vadim I Nazarov & Ivan V Zvyagin & Vitalina I Kirgizova, 2015. "VDJtools: Unifying Post-analysis of T Cell Receptor Repertoires," PLOS Computational Biology, Public Library of Science, vol. 11(11), pages 1-16, November.
    2. Christina Bligaard Pedersen & Søren Helweg Dam & Mike Bogetofte Barnkob & Michael D. Leipold & Noelia Purroy & Laura Z. Rassenti & Thomas J. Kipps & Jennifer Nguyen & James Arthur Lederer & Satyen Har, 2022. "cyCombine allows for robust integration of single-cell cytometry datasets within and across technologies," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
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