Long-term outcome of hematopoietic stem cell transplantation in two children with Mucopolysaccharidosis.
10.3760/cma.j.cn511374-20220429-00298
- Author:
Jianmin WANG
1
;
Jing CHEN
;
Changying LUO
;
Huiwen ZHANG
;
Xuefan GU
;
Weimin ZHANG
Author Information
1. Department of Hematological and Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China. chenjing@scmc.com.cn.
- Publication Type:Journal Article
- MeSH:
Humans;
Child;
Male;
Female;
Infant;
Child, Preschool;
Graft vs Host Disease/etiology*;
China;
Hematopoietic Stem Cell Transplantation/adverse effects*;
Mucopolysaccharidoses/etiology*;
Busulfan;
Treatment Outcome
- From:
Chinese Journal of Medical Genetics
2023;40(12):1489-1495
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the long-term efficacy of allogeneic hematopoietic stem cell transplantation (alloHSCT) in patients with Mucopolysaccharidosis (MPS), which has rarely been reported in China.
METHODS:A 18-month-old boy and a 23-month-old girl undergoing alloHSCT for MPS VI and MPS IH Shanghai Children's Medical Center on March 30, 2006 and September 6, 2006 were selected as the study subjects. A busulfan-based myeloablative regimen was used as the conditioning regimen. Peripheral stem cells were respectively collected from a human leucocyte antigen (HLA) matched sibling carrier donor and a HLA 9/10 matched unrelated donor. Both patients were followed up for more than 15 years. The functions of internal organs before and after the transplantation were compared, and child 1 was also compared with his untreated brother and healthy brother.
RESULTS:Both children have achieved full donor chimerism after the transplantation, and their enzymatic activities have remained stable. The enzymatic activity of the child 1 was slightly lower than normal but similar to that of his carrier donor, whilst that of the child 2 was normal. Both children have attended schools with good academic performance. Compared with his untreated brother, the respiratory function and hearing of child 1 have significantly improved. However, his orthopedic and cardiac disorders have still remained and required medical intervention. For child 2, her obstructive pulmonary disease was resolved and cognitive development was well preserved after the HSCT. Her heart disease has become stabilized and even improved with time, though her corneal clouding and skeletal malformation still required surgery.
CONCLUSION:MPS patients can sustain long-term and stable enzymatic activities after successful alloHSCT. Compared with untreated patients, their health can be significantly improved, along with considerably prolonged survival, though the long-term efficacy of HSCT for different organs may vary to a certain extent.
