First successful bone marrow transplantation for X-linked chronic granulomatous disease by using preimplantation female gender typing and HLA matching

被引:21
|
作者
Reichenbach, Janine [1 ]
Van de Velde, Hilde [2 ]
De Rycke, Martine [3 ]
Staessen, Catherine [3 ]
Platteau, Peter [2 ]
Baetens, Patricia [2 ]
Guengoer, Tayfun [1 ]
Ozsahin, Hulya [4 ]
Scherer, Franziska [1 ]
Siler, Ulrich [1 ]
Seger, Reinhard A. [1 ]
Liebaers, Inge [3 ]
机构
[1] Univ Childrens Hosp Zurich, Div Immunol Hematol BMT, CH-8032 Zurich, Switzerland
[2] UZ Brussels, Ctr Reprod Med, Brussels, Belgium
[3] UZ Brussels, Ctr Med Genet, Brussels, Belgium
[4] Univ Hosp Geneva, Dept Pediat, Div Hematol Oncol, Geneva, Switzerland
关键词
preimplantation genetic diagnosis; hematopoietic stem cell transplantation; chronic granulomatous disease; female sexing; HLA matching;
D O I
10.1542/peds.2008-0123
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Allogeneic hematopoietic stem cell transplantation from an human leukocyte antigen (HLA)-identical donor is currently the only proven curative treatment for chronic granulomatous disease. Hematopoietic stem cell transplantation with alternative donors is associated with higher morbidity and mortality. Therefore, we performed in vitro fertilization and preimplantation HLA matching combined with female sexing for hematopoietic stem cell transplantation in chronic granulomatous disease. Ethical and psychological issues were considered carefully. We used in vitro fertilization with X-enriched spermatozoa followed by preimplantation genetic diagnosis to identify female HLA-genoidentical embryos in a family in need of a suitable donor for their boy affected with severe X-linked chronic granulomatous disease. Two preimplantation genetic diagnosis cycles were performed in the family. In the second cycle, 2 HLA-genoidentical female embryos were transferred and a singleton pregnancy was obtained, resulting in the birth of an unaffected girl at term. Because of insufficient cell numbers in the cord-blood source, conventional hematopoietic stem cell transplantation had to be performed at 12 months of age of the donor and 5(8/12) years of age of the recipient and resulted in complete stable donor chimerism and immunologic reconstitution up to 25 months post-hematopoietic stem cell transplantation. Hematopoietic stem cell transplantation after in vitro fertilization and combined female sexing and HLA matching offers a new and relatively rapid therapeutic option for patients with X-linked primary immunodeficiency such as chronic granulomatous disease who need hematopoietic stem cell transplantation but lack an HLA-genoidentical donor.
引用
收藏
页码:E778 / E782
页数:5
相关论文
共 50 条
  • [31] Correction to: Hematopoietic Stem Cell Transplantation in late-onset X-linked Chronic Granulomatous Disease in a female carrier
    Matteo Trevisan
    Elizabeth M. Kang
    Alberto Tommasini
    Marco Confalonieri
    Journal of Clinical Immunology, 2022, 42 : 1400 - 1400
  • [32] Successful haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide in a child with X-linked chronic granulomatous disease: A first report in Asia
    Janjindamai, Chawisa
    Manuyakorn, Wiparat
    Anurathapan, Usanarat
    Pakakasama, Samart
    Wattanasirichaigoon, Duangrurdee
    Kamchaisatian, Wasu
    Benjaponpitak, Suwat
    Hongeng, Suradej
    ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY, 2022, 40 (03): : 278 - 282
  • [33] Detection of X-linked chronic granulomatous disease variants using dihydrorhodamine assay
    Jirapongsananuruk, O
    Kuhns, DB
    Anderson-Cohen, M
    Brown, MR
    Niemela, JE
    Malech, HL
    Fleisher, TA
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (01) : S277 - S277
  • [34] X-linked chronic granulomatous disease secondary to skewed X-chromosome inactivation in female patients
    Zhang, Yue
    Shu, Zhou
    Li, Yan
    Piao, Yurong
    Sun, Fei
    Han, Tongxin
    Wang, Tianyou
    Mao, Huawei
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2024, 215 (03): : 261 - 267
  • [35] UNEXPECTED DIAGNOSIS OF X-LINKED CHRONIC GRANULOMATOUS DISEASE IN A MIDDLE-AGED FEMALE CARRIER
    Wang, Z.
    Tang, W.
    Sheng, G.
    Kachru, R.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2021, 127 (05) : S106 - S106
  • [36] Successful bone marrow transplantation in 9-month-old patient with chronic granulomatous disease
    Kansoy, S
    Aksoylar, S
    Kutukculer, N
    Kantar, M
    Kavakli, K
    Cetingul, N
    BONE MARROW TRANSPLANTATION, 2003, 31 : S228 - S228
  • [37] Successful bone marrow transplantation in an 8-month-old patient with chronic granulomatous disease
    Kansoy, Savas
    Kuetuekcueler, Necil
    Aksoylar, Serap
    Aksu, Guezide
    Kantar, Mehmet
    Cetinguel, Nazan
    TURKISH JOURNAL OF PEDIATRICS, 2006, 48 (03) : 253 - 255
  • [38] Preimplantation genetic testing for X-linked chronic granulomatous disease induced by a CYBB gene variant: A case report
    Chen, Xinlian
    Peng, Cuiting
    Chen, Han
    Zhou, Fan
    Keqie, Yuezhi
    Li, Yutong
    Liu, Shanling
    Ren, Jun
    MEDICINE, 2024, 103 (05) : E37198
  • [39] CHRONIC GRANULOMATOUS-DISEASE IN AN ADULT FEMALE WITH GRANULOMATOUS CHEILITIS - EVIDENCE FOR AN X-LINKED PATTERN OF INHERITANCE WITH EXTREME LYONIZATION
    DUSI, S
    POLI, G
    BERTON, G
    CATALANO, P
    FORNASA, CV
    PESERICO, A
    ACTA HAEMATOLOGICA, 1990, 84 (01) : 49 - 56
  • [40] X-linked chronic granulomatous disease in a female carrier with novel pathogenic mutation and skewed X-inactivation
    Amaral, Joana Barroso
    Paiva, Artur Augusto
    Ramos, Fabiana Viana
    Stasia, Marie Jose
    Lemos, Sonia Gaspar
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2018, 120 (03) : 328 - 329