Literature DB >> 12621497

Split chimerism after allogeneic bone marrow transplantation in Chediak-Higashi syndrome.

S Yamazaki1, H Takahashi, H Fujii, T Miyamae, M Mori, K Fujioka, T Funabiki, S Yokota, N Arai, K Ikuta.   

Abstract

Chediak-Higashi Syndrome (CHS) is a hereditary multiorgan disease associated with a lymphoproliferative disorder termed 'accelerated phase' (AP). As AP is often life-threatening, hematopoietic stem cell transplantation has been proposed as the only curative treatment for CHS. Here, we report a 1-year-old Japanese boy with CHS who received an HLA-matched unrelated BMT at the AP stage, which resulted in split chimerism. We evaluated the chimerism status of isolated leukocytes and found that only a limited population of T and NK cells was of donor origin and the majority of these and other hematopoietic cells was of host origin. Clinical outcome was successful, and the patient is currently alive and well, free of AP and serious infections more than 18 months after BMT.

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Year:  2003        PMID: 12621497     DOI: 10.1038/sj.bmt.1703789

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  2 in total

1.  Potential large animal models for gene therapy of human genetic diseases of immune and blood cell systems.

Authors:  Thomas R Bauer; Rima L Adler; Dennis D Hickstein
Journal:  ILAR J       Date:  2009

2.  [Umbilical cord blood transplantation in the treatment of Chediak-Higashi syndrome with hemophagocytic syndrome: a case report and literature review].

Authors:  Y Zhang; Z Y Gao; X J Yu; D P Lu
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2017-11-14
  2 in total

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