AI Article Synopsis

  • A study involving 57 pediatric patients (ages 0.5-11.4 years) focused on harvesting autologous hematopoietic stem progenitor cells (HSPC) for gene therapy aimed at certain inherited disorders like ADA-SCID, Wiskott-Aldrich syndrome, and metachromatic leukodystrophy.
  • The research highlighted that a minimum dose of CD34+ cells needed for effective infusion was 2 × 10/kg, with an optimal target of 5-10 × 10/kg, and the average volume of bone marrow harvested was 34.2 ml/kg.
  • Findings indicated that larger volumes (over 30 ml/kg) harvested from children, even infants with these

Article Abstract

Collection of an adequate amount of autologous haematopoietic stem progenitor cells (HSPC) is required for ex vivo manipulation and successful engraftment for certain inherited disorders. Fifty-seven paediatric patients (age 0.5-11.4 years) underwent a bone marrow harvest for the purpose of HSPC gene therapy (GT), including adenosine deaminase-severe combined immunodeficiency (ADA-SCID), Wiskott-Aldrich syndrome (WAS) and metachromatic leukodystrophy (MLD) patients. Total nucleated cells and the percentage and absolute counts of CD34+ cells were calculated at defined steps of the procedure (harvest, CD34+ cell purification, transduction with the gene transfer vector and infusion of the medicinal product). A minimum CD34+ cell dose for infusion was 2 × 10/kg, with an optimal target at 5-10 × 10/kg. Median volume of bone marrow harvested was 34.2 ml/kg (range 14.2-56.6). The number of CD34+ cells collected correlated inversely with weight and age in all patients and particularly in the MLD children group. All patients reached the minimum target dose for infusion: median dose of CD34+ cells/kg infused was 10.3 × 10/kg (3.7-25.9), with no difference among the three groups. Bone marrow harvest of volumes > 30 ml/kg in infants and children with ADA-SCID, WAS and MLD is well tolerated and allows obtaining an adequate dose of a medicinal product for HSPC-GT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897559PMC
http://dx.doi.org/10.1038/s41409-019-0573-6DOI Listing

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