Literature DB >> 12756384

Umbilical cord blood transplantation in Wiskott Aldrich syndrome.

Alan P Knutsen1, Marsha Steffen, Kris Wassmer, Donna A Wall.   

Abstract

OBJECTIVE: To report the use of umbilical cord blood (UCB) stem cell transplantation in Wiskott Aldrich syndrome (WAS) when a matched sibling donor was unavailable.
METHODS: Three children with WAS received unrelated umbilical cord blood stem cell transplantation after a preparative regimen for the treatment of combined immunodeficiency diseases. The patients ranged in age from 1.9 to 7.9 years. The cord blood units were 4/6 HLA antigen matches in 2 children and 5/6 in 1 child, with molecular HLA-DR match in all 3 children.
RESULTS: The time for neutrophil engraftment (ANC >500/mm(3)) was 11 to 16 days, and the average time for platelet engraftment was 36 to 49 days. One patient had no evidence of GvHD, 1 patient grade I, and 1 patient grade II. No patient had chronic GvHD. The patient with grade II GvHD also had gut involvement. Immunologic reconstitution demonstrated that cord blood stem cell transplantation resulted in consistent and stable T-, B-, and NK-cell development. Functional B-cell antibody responses revealed that 2 of the patients in whom IVIG has been discontinued had low detectable antibody responses to tetanus and diphtheria toxoid immunizations at 18 to 24 months after transplantation.
CONCLUSIONS: Unrelated umbilical donor cord blood is an alternative source of stem cells for transplantation in children with WAS when a suitable HLA-matched donor is not available. Benefits of UCB include rapid and reliable recovery of immune function, low risk of GvHD, and low viral transmission rate.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12756384     DOI: 10.1067/mpd.2003.155

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  5 in total

Review 1.  Hematopoietic cell transplantation for Wiskott-Aldrich syndrome: advances in biology and future directions for treatment.

Authors:  Sung-Yun Pai; Luigi D Notarangelo
Journal:  Immunol Allergy Clin North Am       Date:  2010-05       Impact factor: 3.479

2.  Effects of conditioning regimens and T cell depletion in hematopoietic cell transplantation for primary immune deficiency.

Authors:  Brandon M Triplett; Chong Wang; Jie Yang; Mari Dallas; Christine Hartford; Vanessa Howard; Asha Pillai; David Shook; Ashok Srinivasan; Joseph Laver; Wing Leung
Journal:  Biol Blood Marrow Transplant       Date:  2012-07-27       Impact factor: 5.742

3.  Phenotypic and genotypic correction of WASP gene mutation in Wiskott-Aldrich syndrome by unrelated cord blood stem cell transplantation.

Authors:  Young-Ho Lee; Yeon-Jung Lim; Su-Ah Shin; Chang-Hwa Song; Eun-Kyeong Jo; Jin-A Jung; Ha-Baik Lee
Journal:  J Korean Med Sci       Date:  2009-07-30       Impact factor: 2.153

4.  Successful unrelated cord blood transplantation in an infant with Wiskott-Aldrich syndrome following recurrent cytomegalovirus disease.

Authors:  Michiya Kaneko; Tsutomu Watanabe; Hiroyoshi Watanabe; Masahiro Kimura; Hiroko Suzuya; Yasuhiro Okamoto; Ryuji Nakagawa; Yasuhiro Kuroda
Journal:  Int J Hematol       Date:  2003-12       Impact factor: 2.490

5.  A risk factor analysis of outcomes after unrelated cord blood transplantation for children with Wiskott-Aldrich syndrome.

Authors:  Zhanna Shekhovtsova; Carmem Bonfim; Annalisa Ruggeri; Samantha Nichele; Kristin Page; Amal AlSeraihy; Francisco Barriga; José Sánchez de Toledo Codina; Paul Veys; Jaap Jan Boelens; Karin Mellgren; Henrique Bittencourt; Tracey O'Brien; Peter J Shaw; Alicja Chybicka; Fernanda Volt; Federica Giannotti; Eliane Gluckman; Joanne Kurtzberg; Andrew R Gennery; Vanderson Rocha
Journal:  Haematologica       Date:  2017-03-02       Impact factor: 9.941

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.