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Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humans.
Izotova, Natalia; Rivat, Christine; Baricordi, Cristina; Blanco, Elena; Pellin, Danilo; Watt, Eleanor; Gkazi, Athina S; Adams, Stuart; Gilmour, Kimberly; Bayford, Jinhua; Booth, Claire; Gaspar, H Bobby; Thrasher, Adrian J; Biasco, Luca.
Afiliación
  • Izotova N; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
  • Rivat C; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
  • Baricordi C; Orchard Therapeutics, University College of London (UCL), London, UK.
  • Blanco E; Gene Therapy Program, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Pellin D; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
  • Watt E; Gene Therapy Program, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA.
  • Gkazi AS; Great Ormond Street Hospital, London, UK.
  • Adams S; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
  • Gilmour K; Great Ormond Street Hospital, London, UK.
  • Bayford J; Great Ormond Street Hospital, London, UK.
  • Booth C; Great Ormond Street Hospital, London, UK.
  • Gaspar HB; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
  • Thrasher AJ; Great Ormond Street Hospital, London, UK.
  • Biasco L; Great Ormond Street Institute of Child Health Faculty of Population Health Sciences, London, UK.
Nat Commun ; 12(1): 1622, 2021 03 12.
Article en En | MEDLINE | ID: mdl-33712608
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Asesinas Naturales / Linfocitos / Linfocitos T / Células Progenitoras Linfoides Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Asesinas Naturales / Linfocitos / Linfocitos T / Células Progenitoras Linfoides Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido
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