Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (45): 8460-8463.doi: 10.3969/j.issn.1673-8225.2010.45.023

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Related factors affecting peripheral blood CD34+ cell purification

Bai Wen, Bai Bin, Wang Li-ming, Zhou Jian-jun, Zhang Cong, Liu Tao    

  1. Cell Therapy Center, the 323 Hospital of Chinese PLA, Xi’an  710054, Shaanxi Province, China  
  • Online:2010-11-05 Published:2010-11-05
  • Contact: Wang Li-ming, Master, Chief physician, Cell Therapy Center, the 323 Hospital of Chinese PLA, Xi’an 710054, Shaanxi Province, China wanglm@fmmu.edu.cn
  • About author:Bai Wen, Associate chief technician, Cell Therapy Center, the 323 Hospital of Chinese PLA, Xi’an 710054, Shaanxi Province, China bai_wen_323@126.com

Abstract:

BACKGROUND: Hemopoietic stem cells have the potential of self replication and renewal. CD34+ cells have the marker of hemopoietic stem cells.
OBJECTIVE: To analyze the related factors that affect the peripheral blood CD34+ cell purification.
METHODS: From 90 cases of patients, the peripheral blood were collected, after human granulocyte colony stimulating factor (G-CSF) 5 μg/kg•d mobilizing for 1-3 days, using COBE machine mononuclear cells fluid 80-100 mL was collcected, the CD34 stem cells were purified by Clini MACS.
RESULTS AND CONCLUSION: The mean value of CD34+ cells was (1.73±1.15)×107 in 90 cases. Using flow cytometry, the positive rate of CD34+ cells was more than 80%. When the circulation blood liquid singly collected by COBE machine was 980- 1 100 mL, it was useful for CD34+ cells collection (P = 0.005). After mobilizing, when the white blood cell concentration was (16-21)×109/L, it was useful for CD34+ cells collection (P < 0.05);  when the general ratio of middle cells to lymphocytes was more than 11%, it was useful for CD34+ cell collection (P < 0.05).  When the concentration of blood platelet in mononuclear cells was less than 2 100×109/L, it was useful for CD34+ cell collection (P < 0.05); when the patient’s age was younger than 16 years, the number of collected CD34+ cells was high (P = 0.003). Moreover, the temperature of CD34+ cells, the magnetism marker, the eccentricity of treating cells, all could affect the CD34+ cells collection. Results indicate that the CD34+ cells purified by Clini MACS machine could fit the clinical need and keep good experiment stability and repeatability. To improve the CD34+ cells collection, the related factors which affect the peripheral blood CD34+ purification should be carefully considered.

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