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同种异体干细胞移植使用清髓性和强度降低的预处理方案治疗主要组织相容性复合体 II 类缺陷患者。

Allogeneic stem cell transplantation using myeloablative and reduced-intensity conditioning in patients with major histocompatibility complex class II deficiency.

机构信息

Section of Pediatric Allergy and Immunology, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

出版信息

Biol Blood Marrow Transplant. 2010 Jun;16(6):818-23. doi: 10.1016/j.bbmt.2010.01.002. Epub 2010 Jan 14.

Abstract

Major histocompatibility complex class II (MHC II) deficiency is a rare combined immunodeficiency disease. Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment. Between June 1994 and February 2007, 30 children with MHC II deficiency underwent a total of 33 HSCT procedures. Median age at HSCT was 27 months. The stem cell source was unmanipulated bone marrow from HLA-identical related donors in 26 patients, one HLA antigen-mismatched bone marrow in 3 patients, and unrelated umbilical cord blood in 1 patient. Conditioning was with one of 3 myeloablative regimens--regimen A (18 patients): busulfan (Bu), cyclophosphamide (Cy), and etoposide; regimen B (2 patients): Bu, Cy, and antithymocyte globulin (ATG); or regimen C (1 patient): CY and total body irradiation (TBI)--or with a reduced-intensity regimen (12 patients): fludarabine, melphalan, and ATG. The median CD34 cell dose was 8.3 x 10(6)/kg. Twenty patients experienced immune reconstitution and had sustained engraftment ranging from 9% to 100% for lymphoid lines and from 5% to 100% for myeloid lines that were significant to cure the disease. The overall disease-free survival rate was 66% and 76% after HLA-identical HSCT, with a median follow-up of 6.3 years, which is higher than previously reported. In HLA-identical transplant recipients, reliable donor stem cell engraftment and immune reconstitution were achieved through myeloablative or reduced-intensity conditioning. Further studies and long-term follow-up are needed to determine the appropriate conditioning regimen.

摘要

主要组织相容性复合体 II 类(MHC II)缺陷是一种罕见的联合免疫缺陷病。异基因造血干细胞移植(HSCT)是唯一的治愈性治疗方法。1994 年 6 月至 2007 年 2 月,30 例 MHC II 缺陷患儿共进行了 33 次 HSCT 手术。HSCT 时的中位年龄为 27 个月。干细胞来源为 26 例 HLA 完全匹配的相关供者未处理的骨髓、3 例 HLA 抗原错配的骨髓和 1 例无关脐血。预处理方案为 3 种清髓性方案之一:方案 A(18 例):白消安(Bu)、环磷酰胺(Cy)和依托泊苷;方案 B(2 例):Bu、Cy 和抗胸腺细胞球蛋白(ATG);或方案 C(1 例):Cy 和全身照射(TBI)-或采用强度降低的方案(12 例):氟达拉滨、美法仑和 ATG。中位 CD34 细胞剂量为 8.3 x 10(6)/kg。20 例患者发生免疫重建,获得持续的嵌合,从 9%到 100%的淋巴系和从 5%到 100%的髓系嵌合,这对治愈疾病具有重要意义。在 HLA 完全匹配的 HSCT 后,无病生存率分别为 66%和 76%,中位随访时间为 6.3 年,高于既往报道。在 HLA 完全匹配的移植受者中,通过清髓性或强度降低的预处理实现了可靠的供者干细胞植入和免疫重建。需要进一步研究和长期随访来确定合适的预处理方案。

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