Outcomes of patients with severe combined immunodeficiency treated with hematopoietic stem cell transplantation with and without preconditioning

被引:37
作者
Patel, Niraj C. [1 ]
Chinen, Javier [1 ]
Rosenblatt, Howard M. [2 ]
Hanson, I. Celine [1 ]
Krance, Robert A. [3 ]
Paul, Mary E. [1 ]
Abramson, Stuart L. [1 ]
Noroski, Lenora M. [1 ]
Davis, Carla M. [1 ]
Seeborg, Filiz O. [1 ]
Foster, Samuel B. [1 ]
Leung, Kathryn S. [3 ]
Brown, Betty S. [1 ]
Ritz, Jerome [4 ,5 ,6 ]
Shearer, William T. [1 ]
机构
[1] Texas Childrens Hosp, Dept Pediat, Sect Allergy & Immunol, Baylor Coll Med, Houston, TX 77039 USA
[2] Dell Childrens Med Ctr Cent Texas, Austin, TX USA
[3] Texas Childrens Hosp, Sect Hematol & Oncol, Baylor Coll Med, Houston, TX 77039 USA
[4] Harvard Univ, Sch Med, Div Hematol Malignancies, Boston, MA USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Harvard Stem Cell Inst, Boston, MA USA
关键词
Hematopoietic stem cell transplantation; graft-versus-host disease; severe combined immunodeficiency; immune reconstitution; primary immunodeficiency; conditioning; BONE-MARROW-TRANSPLANTATION; IMMUNE RECONSTITUTION; SINGLE-CENTER; DEFICIENCY; BMT;
D O I
10.1016/j.jaci.2009.08.041
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The effect of pretransplantation conditioning on the long-term outcomes of patients receiving hematopoietic stem cell transplantation for severe combined immunodeficiency (SCID) has not been completely determined. Objective: We sought to assess the outcomes of 23 mostly conditioned patients with SCID and compare their outcomes with those of 25 previously reported nonconditioned patients with SCID who underwent transplantation. Methods: In the present study we reviewed the medical records of these 23 consecutive, mostly conditioned patients with SCID who underwent transplantation between 1998 and 2007. Results: Eighteen patients (median age at transplantation, 10 months; range, 0.8-108 months) received haploidentical mismatched related donor, matched unrelated donor, or mismatched unrelated donor transplants, 17 of whom received pretransplantation conditioning (with I not conditioned); 13 (72%) patients engrafted with donor cells and survive at a median of 3.8 years (range, 1.8-9.8 year); 5 (38%) of 13 patients require intravenous immunoglobulin; and 6 of 6 age-eligible children attend school. Of 5 recipients (median age at transplantation, 7 months; range, 2-23 months) of matched related donor transplants, all 5 engrafted and survive at a median of 7.5 years (range, 1.5-9.5 year), I recipient requires intravenous immunoglobulin, and 3 of 3 age-eligible children attend school. Gene mutations were known in 16 cases: mutation in the common gamma chain of the IL-2 receptor (IL2RG) in 7 patients, mutation in the alpha chain of the IL-7 receptor (IL7RA) in 4 patients, mutation in the recombinase-activating gene (RAG1) in 2 patients, adenosine deaminase deficiency (ADA) in 2 patients, and adenylate kinase 2 (AK2) in I patient. Early outcomes and quality of life of the previous nonconditioned versus the present conditioned cohorts were not statistically different, but longer-term follow-up is necessary for confirmation. Conclusions: Hematopoietic stem cell transplantation in patients with SCED results in engraftment, long-term survival, and a good quality of life for the majority of patients with or without pretransplantation conditioning. (J Allergy Clin Immunol 2009;124:1062-9.)
引用
收藏
页码:1062 / 1069
页数:8
相关论文
共 17 条
[1]   Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies:: report of the European experience 1968-99 [J].
Antoine, C ;
Müller, S ;
Cant, A ;
Cavazzana-Calvo, M ;
Veys, P ;
Vossen, J ;
Fasth, A ;
Heilmann, C ;
Wulffraat, N ;
Seger, R ;
Blanche, S ;
Friedrich, W ;
Abinun, M ;
Davies, G ;
Bredius, R ;
Schulz, A ;
Landais, P ;
Fischer, A .
LANCET, 2003, 361 (9357) :553-560
[2]   Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell-depleted bone marrow transplantation - A retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society for Immunodeficiency [J].
Bertrand, Y ;
Landais, P ;
Friedrich, W ;
Gerritsen, B ;
Morgan, G ;
Fasth, A ;
Cavazzana-Calvo, M ;
Porta, F ;
Cant, A ;
Espanol, T ;
Müller, S ;
Veys, P ;
Vossen, J ;
Haddad, E ;
Fischer, A .
JOURNAL OF PEDIATRICS, 1999, 134 (06) :740-748
[3]  
BREARD J, 1980, J IMMUNOL, V124, P1943
[4]   Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency [J].
Buckley, RH ;
Schiff, SE ;
Schiff, RI ;
Markert, ML ;
Williams, LW ;
Roberts, JL ;
Myers, LA ;
Ward, FE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (07) :508-516
[5]   Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution [J].
Buckley, RH .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :625-655
[6]  
BUCKLEY RH, 1986, J IMMUNOL, V136, P2398
[7]   In vitro T cell depletion using Campath 1M for mismatched BMT for severe combined immunodeficiency (SCID) [J].
Dickinson, AM ;
Reid, MM ;
Abinun, M ;
Peak, J ;
Brigham, K ;
Dunn, J ;
Cant, AJ .
BONE MARROW TRANSPLANTATION, 1997, 19 (04) :323-329
[8]   Severe combined immunodeficiency.: A model disease for molecular immunology and therapy [J].
Fischer, A ;
Le Deist, F ;
Hacein-Bey-Abina, S ;
André-Schmutz, I ;
Basile, GD ;
de Villartay, JP ;
Cavazzana-Calvo, M .
IMMUNOLOGICAL REVIEWS, 2005, 203 :98-109
[9]   Bone marrow transplantation for severe combined immune deficiency [J].
Grunebaum, E ;
Mazzolari, E ;
Porta, F ;
Dallera, D ;
Atkinson, A ;
Reid, B ;
Notarangelo, LD ;
Roifman, CM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (05) :508-518
[10]   Long-term chimerism and B-cell function after bone marrow transplantation in patients with severe combined immunodeficiency with B cells: A single-center study of 22 patients [J].
Haddad, E ;
Le Deist, F ;
Aucouturier, P ;
Cavazzana-Calvo, M ;
Blanche, S ;
De Saint Basile, G ;
Fischer, A .
BLOOD, 1999, 94 (08) :2923-2930