Effects and long-term follow-up of using umbilical cord blood-derived mesenchymal stromal cells in pediatric patients with severe BK virus-associated late-onset hemorrhagic cystitis after unrelated cord blood transplantation.
Juan TongHuiLan LiuChangCheng ZhengXiaoYu ZhuBaoLin TangXiang WanWen YaoKaiDi SongLei ZhangXuHan ZhangZiMin SunPublished in: Pediatric transplantation (2020)
This is a retrospective study to evaluate the efficacy and safety of umbilical cord blood-derived mesenchymal stromal cells (MSCs) for the treatment of pediatric patients with severe BK virus-associated late-onset hemorrhagic cystitis (BKV-HC) after unrelated cord blood transplantation (UCBT). Thirteen pediatric patients with severe BKV-HC from December 2013 to December 2015 were treated with MSCs. The number of MSCs transfused in each session was 1 × 106 /kg once a week until the symptoms improved. The median follow-up time was 1432 (89-2080) days. The median frequency of MSC infusion was 2 (1-3), with eight cured cases and five effective cases; the total efficacy rate was 100%. The copy number of urine BKV DNA was 4.43 (0.36-56.9) ×108 /mL before MSC infusion and 2.67 (0-56.3) ×108 /mL after MSC infusion; the difference was not significant (P = .219). There were no significant differences in the overall survival, disease-free survival, and the incidence of relapse and acute and chronic graft-versus-host disease between the MSC infusion group and non-MSC infusion group. There was also no significant difference in the cytomegalovirus, Epstein-Barr virus (EBV), and fungal and bacterial infection rates between the two groups. Although umbilical cord blood-derived MSCs do not reduce the number of BKV DNA copies in the urine, the cells have a high efficacy rate and minimal side effects in treating severe BKV-HC after UCBT among pediatric patients. MSCs do not affect the rates of relapse, long-term infection, or survival of patients with leukemia.
Keyphrases
- umbilical cord
- cord blood
- late onset
- mesenchymal stem cells
- free survival
- early onset
- epstein barr virus
- bone marrow
- copy number
- low dose
- cell therapy
- diffuse large b cell lymphoma
- drug induced
- mitochondrial dna
- liver failure
- genome wide
- circulating tumor
- risk factors
- gene expression
- dna methylation
- clinical trial
- acute myeloid leukemia
- intensive care unit
- randomized controlled trial
- young adults
- physical activity
- replacement therapy
- sleep quality
- mechanical ventilation
- study protocol