• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

获得性再生障碍性贫血的移植物排斥反应及二次骨髓移植:欧洲骨髓移植组再生障碍性贫血工作组报告

Graft rejection and second bone marrow transplants for acquired aplastic anaemia: a report from the Aplastic Anaemia Working Party of the European Bone Marrow Transplant Group.

作者信息

McCann S R, Bacigalupo A, Gluckman E, Hinterberger W, Hows J, Ljungman P, Marin P, Nissen C, van't Veer Kerthof E, Raghavachar A

机构信息

Department of Haematology, St. James Hospital, Dublin, Ireland.

出版信息

Bone Marrow Transplant. 1994 Mar;13(3):233-7.

PMID:8199566
Abstract

Six hundred and eighteen patients with acquired aplastic anaemia grafted from an HLA-identical sibling donor between 1976 and 1990 in eight European centres were reported to the Working Party for Severe Aplastic Anaemia (SAA) Registry and were evaluable for analysis of the incidence of graft failure/rejection and the outcome of second bone marrow transplants (BMT). The number of patients experiencing graft rejection declined significantly over the study period from 32% to 8% (p < 0.0001). This coincided with the introduction of cyclosporine to the conditioning regimen for BMT. The graft rejection rate in the post-hepatitis SAA group was significantly lower than in the group with idiopathic SAA (4% vs 20%) (p = 0.001). The use of irradiation in the conditioning regimen significantly reduced the number of patients experiencing graft rejection (7% vs 21%) (p = 0.004). Age, sex and severity of disease did not influence the rate of sustained engraftment. Of the 85 patients experiencing graft rejection, 41 received a second transplant: their survival is 33% vs 8% for patients not transplanted a second time (p = 0.003). The major factor predicting the outcome of second BMT for SAA was the interval from first BMT. Patients receiving a second BMT within 60 days from the first BMT had a significantly poorer outcome.

摘要

1976年至1990年间,欧洲8个中心有618例获得性再生障碍性贫血患者接受了来自HLA相合同胞供者的移植,并被报告给严重再生障碍性贫血(SAA)登记工作组,可用于分析移植失败/排斥的发生率以及第二次骨髓移植(BMT)的结果。在研究期间,发生移植排斥的患者数量从32%显著下降至8%(p<0.0001)。这与环孢素被引入BMT预处理方案的时间相吻合。肝炎后SAA组的移植排斥率显著低于特发性SAA组(4%对20%)(p=0.001)。预处理方案中使用放疗显著减少了发生移植排斥的患者数量(7%对21%)(p=0.004)。年龄、性别和疾病严重程度不影响持续植入率。在85例发生移植排斥的患者中,41例接受了第二次移植:他们的生存率为33%,而未接受第二次移植的患者为8%(p=0.003)。预测SAA第二次BMT结果的主要因素是距首次BMT的时间间隔。在首次BMT后60天内接受第二次BMT的患者结局明显较差。

相似文献

1
Graft rejection and second bone marrow transplants for acquired aplastic anaemia: a report from the Aplastic Anaemia Working Party of the European Bone Marrow Transplant Group.获得性再生障碍性贫血的移植物排斥反应及二次骨髓移植:欧洲骨髓移植组再生障碍性贫血工作组报告
Bone Marrow Transplant. 1994 Mar;13(3):233-7.
2
Bone marrow transplantation for severe aplastic anemia: the Barcelona Hospital Clinic experience.严重再生障碍性贫血的骨髓移植:巴塞罗那医院诊所的经验
Haematologica. 1999 Jan;84(1):26-31.
3
BMT for severe aplastic anemia using cyclosporine.使用环孢素治疗重型再生障碍性贫血的骨髓移植
Bone Marrow Transplant. 1993 Jun;11(6):459-64.
4
Bone marrow transplantation for severe aplastic anemia from donors other than HLA identical siblings: a report of the BMT Working Party.非 HLA 全相合同胞供者的严重再生障碍性贫血骨髓移植:骨髓移植工作组报告
Bone Marrow Transplant. 1988 Nov;3(6):531-5.
5
Allogeneic bone marrow transplantation for severe aplastic anemia: the Vancouver experience.严重再生障碍性贫血的异基因骨髓移植:温哥华的经验。
Clin Invest Med. 1995 Apr;18(2):122-30.
6
Survival of patients with documented autologous recovery after SCT for severe aplastic anemia: a study by the WPSAA of the EBMT.SCT 治疗重型再生障碍性贫血后有自体造血恢复记录的患者的生存:来自 EBMT 的 WPSAA 的研究。
Bone Marrow Transplant. 2010 Jun;45(6):1008-13. doi: 10.1038/bmt.2009.296. Epub 2009 Nov 16.
7
Preceding immunosuppressive therapy with antithymocyte globulin and ciclosporin increases the incidence of graft rejection in children with aplastic anaemia who underwent allogeneic bone marrow transplantation from HLA-identical siblings.在接受来自 HLA 同型同胞的异基因骨髓移植的再生障碍性贫血儿童中,术前使用抗胸腺细胞球蛋白和环孢素进行免疫抑制治疗会增加移植排斥反应的发生率。
Br J Haematol. 2006 Dec;135(5):693-6. doi: 10.1111/j.1365-2141.2006.06352.x. Epub 2006 Oct 19.
8
CsA-based post-graft immunosuppression: the main factor for improving outcome of allografted patients with acquired aplastic anemia. A retrospective survey by the Spanish Group of Hematopoietic Transplantation.基于环孢素A的移植后免疫抑制:改善获得性再生障碍性贫血同种异体移植患者预后的主要因素。西班牙造血移植小组的一项回顾性调查。
Bone Marrow Transplant. 2002 Feb;29(3):205-11. doi: 10.1038/sj.bmt.1703349.
9
Aetiology of severe aplastic anaemia and outcome after allogeneic bone marrow transplantation or immunosuppression therapy. Working Party on Severe Aplastic Anaemia of the European Blood and Marrow Transplantation Group.重型再生障碍性贫血的病因及异基因骨髓移植或免疫抑制治疗后的结局。欧洲血液和骨髓移植组重型再生障碍性贫血工作组
Eur J Haematol Suppl. 1996;60:16-9.
10
Successful allogeneic hematopoietic stem cell transplantation using triple agent immunosuppression in severe aplastic anemia patients.在重型再生障碍性贫血患者中使用三联免疫抑制剂进行成功的异基因造血干细胞移植。
Bone Marrow Transplant. 2003 Jan;31(2):79-86. doi: 10.1038/sj.bmt.1703786.

引用本文的文献

1
Outcomes Following Second Allogeneic Stem Cell Transplant for Graft Failure or Poor Graft Function: A Single Centre Experience.第二次异基因干细胞移植治疗移植物失败或移植物功能不良后的结局:单中心经验
Stem Cell Rev Rep. 2025 Jun 5. doi: 10.1007/s12015-025-10903-x.
2
The outcomes of second haploidentical donor transplantation for graft failure in patients with severe aplastic anaemia.严重再生障碍性贫血患者移植物失败后二次单倍型相合供体移植的结果
Ann Hematol. 2025 Jun 4. doi: 10.1007/s00277-025-06440-9.
3
Graft failure after allogeneic hematopoietic stem cell transplantation in pediatric patients with acute leukemia: autologous reconstitution or second transplant?
急性白血病患儿异基因造血干细胞移植后的移植物失败:自体重建还是二次移植?
Stem Cell Res Ther. 2024 Apr 22;15(1):111. doi: 10.1186/s13287-024-03726-z.
4
Outcome of Second Allogeneic HSCT for Patients with Inborn Errors of Immunity: Retrospective Study of 20 Years' Experience.同种异体 HSCT 治疗原发性免疫缺陷病的疗效:20 年回顾性研究
J Clin Immunol. 2023 Nov;43(8):1812-1826. doi: 10.1007/s10875-023-01549-w. Epub 2023 Jul 14.
5
Pathogenicity and impact of HLA class I alleles in aplastic anemia patients of different ethnicities.不同种族再生障碍性贫血患者 HLA Ⅰ类等位基因的致病性和影响。
JCI Insight. 2022 Nov 22;7(22):e163040. doi: 10.1172/jci.insight.163040.
6
Salvage HLA-haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide for graft failure in non-malignant disorders.挽救性 HLA 单倍体相合造血干细胞移植联合移植后环磷酰胺治疗非恶性疾病移植物失败。
Bone Marrow Transplant. 2021 Sep;56(9):2248-2258. doi: 10.1038/s41409-021-01323-9. Epub 2021 May 9.
7
Graft failure.移植物失败。
Bone Marrow Transplant. 2020 Oct;55(10):1888-1889. doi: 10.1038/s41409-020-0860-2. Epub 2020 Mar 11.
8
Bone Marrow-Derived Mesenchymal Stromal Cells: A Novel Target to Optimize Hematopoietic Stem Cell Transplantation Protocols in Hematological Malignancies and Rare Genetic Disorders.骨髓来源的间充质基质细胞:优化血液系统恶性肿瘤和罕见遗传疾病造血干细胞移植方案的新靶点。
J Clin Med. 2019 Dec 18;9(1):2. doi: 10.3390/jcm9010002.
9
Feasibility of salvage cord blood transplantation using a fludarabine, melphalan, and low-dose anti-thymocyte globulin conditioning regimen.采用氟达拉滨、美法仑和低剂量抗胸腺细胞球蛋白预处理方案进行挽救性脐血移植的可行性。
Int J Hematol. 2019 Apr;109(4):463-469. doi: 10.1007/s12185-019-02610-4. Epub 2019 Feb 8.
10
Allogeneic Matched Related Donor Bone Marrow Transplantation for Pediatric Patients With Severe Aplastic Anemia Using "Low-dose" Cyclophosphamide, ATG Plus Fludarabine.使用“低剂量”环磷酰胺、抗胸腺细胞球蛋白加氟达拉滨对患有严重再生障碍性贫血的儿科患者进行异基因匹配相关供体骨髓移植。
J Pediatr Hematol Oncol. 2018 May;40(4):e220-e224. doi: 10.1097/MPH.0000000000001106.