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Updated: Aug 10, 2026

Pan-myeloid Differentiation of Human Cord Blood Derived CD34+ Hematopoietic Stem and Progenitor Cells
Published on: August 9, 2019
Peripheral blood progenitor cell collection by large-volume leukapheresis in low-weight children
1Department of Pediatric Hematology and Oncology, Hospital Infantil Niño Jesús, Autonomous University of Madrid, Spain.
Insights
Large-volume leukapheresis (LVL) safely collects sufficient peripheral blood progenitor cells (PBPC) in children weighing under 25 kg. This method ensures rapid engraftment and hematologic recovery post-transplantation.
Area of Science:
- Pediatric Hematology
- Cellular Therapy
- Oncology
Background:
- Peripheral blood progenitor cell (PBPC) collection is crucial for pediatric cancer transplantation.
- Large-volume leukapheresis (LVL) is a method for collecting PBPCs, but its application in small children is less established.
Purpose of the Study:
- To evaluate the safety and efficacy of LVL for PBPC collection in pediatric patients weighing 25 kg or less.
- To assess the adequacy of PBPC yield for transplantation and subsequent engraftment kinetics.
Main Methods:
- LVL was performed using a COBE Spectra device in 32 children (10 months-8 years, < or = 25 kg) with malignancies.
- PBPC harvesting commenced after G-CSF cytokine stimulation.
- Modified lymphocytapheresis program with specific anticoagulant (ACD) protocols and flow rates were employed.
Main Results:
- 37 apheresis procedures were conducted; 84% of patients achieved adequate PBPC yield in a single session.
- Median yields included 7.7 x 10(8) MNC/kg, 5.4 x 10(6) CD34+/kg, and 6.2 x 10(4) CFU-GM/kg.
- No significant side effects were observed; LVL was well tolerated. Rapid and sustained engraftment was achieved in 27 transplanted patients.
Conclusions:
- LVL is a safe, well-tolerated, and effective method for PBPC collection in small children.
- This technique facilitates adequate cell collection for transplantation, leading to rapid hematologic recovery.
- CD34+ cell dose positively correlates with engraftment speed.
Abstract:
Large-volume leukapheresis (LVL), defined as the processing of at least three blood volumes in a single session for peripheral blood progenitor cell (PBPC) collection, was performed in 32 small children weighing < or = 25 kg, aged 10 months to 8 years, with a variety of malignancies. Harvesting of PBPC was started after 4 days of cytokine (G-CSF, 12 micrograms/kg s.c.) alone. Procedures were performed using a continuous flow blood cell separator (COBE Spectra). The automated program of lymphocytapheresis was modified to achieve a collection rate of 0.9 ml/min. The extracorporeal line was primed with a unit of a packed red blood cells before the procedure. Acid citrate dextrose (ACD) was used as anticoagulant with an ACD inlet ratio of 1:14 and an ACD infusion rate of 1.1 ml/min/L of total blood volume. The inlet flow ranged between 6 and 35 ml/min (median 20 ml/min). A total of 37 apheresis procedures were performed (median 1, range 1-3). In 84% of patients, a single apheresis yields the minimum number of PBPC cells required for transplantation. No consistent side effects were observed, and LVL was well tolerated by children. A median of 7.7 x 10(8) kg MNC, 5.4 x 10(6)/kg CD34+, and 6.2 x 10(4)/kg CFU-GM per apheresis were harvested. Patients with neuroblastoma had a significantly lower yield than other patients. To date, 27 patients have been transplanted after myeloablative treatment, and rapid and sustained engraftment was achieved in all cases. The number of CD34+ cells infused was highly correlated with engraftment kinetics. LVL can be safely and easily performed in small children, allowing adequate PBPC collection for transplantation with rapid hematologic recovery.
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