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Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans

Author

Listed:
  • Natalia Izotova

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences)

  • Christine Rivat

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences
    University College of London (UCL))

  • Cristina Baricordi

    (Harvard Medical School)

  • Elena Blanco

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences)

  • Danilo Pellin

    (Harvard Medical School)

  • Eleanor Watt

    (Great Ormond Street Hospital)

  • Athina S. Gkazi

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences)

  • Stuart Adams

    (Great Ormond Street Hospital)

  • Kimberly Gilmour

    (Great Ormond Street Hospital)

  • Jinhua Bayford

    (Great Ormond Street Hospital)

  • Claire Booth

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences
    Great Ormond Street Hospital)

  • H. Bobby Gaspar

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences
    University College of London (UCL))

  • Adrian J. Thrasher

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences
    Great Ormond Street Hospital)

  • Luca Biasco

    (Great Ormond Street Institute of Child Health Faculty of Population Health Sciences
    Harvard Medical School)

Abstract

Our mathematical model of integration site data in clinical gene therapy supported the existence of long-term lymphoid progenitors capable of surviving independently from hematopoietic stem cells. To date, no experimental setting has been available to validate this prediction. We here report evidence of a population of lymphoid progenitors capable of independently maintaining T and NK cell production for 15 years in humans. The gene therapy patients of this study lack vector-positive myeloid/B cells indicating absence of engineered stem cells but retain gene marking in both T and NK. Decades after treatment, we can still detect and analyse transduced naïve T cells whose production is likely maintained by a population of long-term lymphoid progenitors. By tracking insertional clonal markers overtime, we suggest that these progenitors can support both T and NK cell production. Identification of these long-term lymphoid progenitors could be utilised for the development of next generation gene- and cancer-immunotherapies.

Suggested Citation

  • Natalia Izotova & Christine Rivat & Cristina Baricordi & Elena Blanco & Danilo Pellin & Eleanor Watt & Athina S. Gkazi & Stuart Adams & Kimberly Gilmour & Jinhua Bayford & Claire Booth & H. Bobby Gasp, 2021. "Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans," Nature Communications, Nature, vol. 12(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21834-9
    DOI: 10.1038/s41467-021-21834-9
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