用于X连锁凋亡抑制蛋白缺陷型噬血细胞性淋巴组织细胞增生症的干扰素γ阻断、苏消安预处理及αβ T细胞去除的外周血干细胞移植 - Suppr | 超能文献

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IFNɣ Block, Treosulfan Conditioning and αβ T Cell Deplete PBSCT for XIAP-Deficient HLH.用于X连锁凋亡抑制蛋白缺陷型噬血细胞性淋巴组织细胞增生症的干扰素γ阻断、苏消安预处理及αβ T细胞去除的外周血干细胞移植

J Clin Immunol. 2017 Aug;37(6):511-513. doi: 10.1007/s10875-017-0413-7. Epub 2017 Jun 21.

2

Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.XIAP 缺陷的异基因造血细胞移植：国际调查显示预后不良。

Blood. 2013 Feb 7;121(6):877-83. doi: 10.1182/blood-2012-06-432500. Epub 2012 Nov 6.

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Complications of Reduced Intensity Conditioning HSCT for XIAP Deficiency (Alloimmune Cytopenias and HLH) Successfully Managed With Donor Lymphocyte Infusion.低强度预处理造血干细胞移植治疗 XIAP 缺陷（同种免疫性血细胞减少症和噬血细胞性淋巴组织细胞增生症）的并发症通过供体淋巴细胞输注成功处理。

J Pediatr Hematol Oncol. 2015 Apr;37(3):e198-9. doi: 10.1097/MPH.0000000000000191.

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Successful stem cell transplant with antibody-based conditioning for XIAP deficiency with refractory hemophagocytic lymphohistiocytosis.采用基于抗体的预处理方案成功进行干细胞移植治疗伴有难治性噬血细胞性淋巴组织细胞增生症的XIAP缺陷症。

Blood. 2013 Jun 13;121(24):4966-8. doi: 10.1182/blood-2013-01-478735.

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Unrelated CD3/CD19-depleted peripheral stem cell transplantation for Hurler syndrome.无关供者CD3/CD19去除的外周血干细胞移植治疗黏多糖贮积症I型（Hurler综合征）

Pediatr Hematol Oncol. 2014 Nov;31(8):723-30. doi: 10.3109/08880018.2014.939794. Epub 2014 Aug 12.

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TCR-alpha/beta and CD19 depletion and treosulfan-based conditioning regimen in unrelated and haploidentical transplantation in children with acute myeloid leukemia.TCR-α/β和CD19清除以及基于曲奥舒凡的预处理方案用于儿童急性髓系白血病非亲缘及单倍体移植

Bone Marrow Transplant. 2016 May;51(5):668-74. doi: 10.1038/bmt.2015.343. Epub 2016 Jan 25.

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Addition of treosulfan to a nonmyeloablative conditioning regimen results in enhanced chimerism and immunologic tolerance in an experimental allogeneic bone marrow transplant model.在非清髓性预处理方案中添加苏消安可增强实验性异基因骨髓移植模型中的嵌合状态和免疫耐受。

Biol Blood Marrow Transplant. 2004 Apr;10(4):236-45. doi: 10.1016/j.bbmt.2003.11.004.

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[An X-linked lymphoproliferative syndrome (XLP) caused by mutations in the inhibitor-of-apoptosis gene XIAP].由凋亡抑制基因XIAP突变引起的X连锁淋巴细胞增生综合征（XLP）

Med Sci (Paris). 2007 Mar;23(3):235-7. doi: 10.1051/medsci/2007233235.

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The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency.XIAP缺乏症婴儿极早发型小肠结肠炎的诊断挑战。

BMC Pediatr. 2015 Dec 15;15:208. doi: 10.1186/s12887-015-0522-5.

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X-linked Inhibitor of Apoptosis Complicated by Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) and Granulomatous Hepatitis.X连锁凋亡抑制因子并发肉芽肿性淋巴细胞间质性肺病（GLILD）和肉芽肿性肝炎。

J Clin Immunol. 2016 Oct;36(7):733-8. doi: 10.1007/s10875-016-0320-3. Epub 2016 Aug 5.

引用本文的文献

1

Evolution of Our Understanding of XIAP Deficiency.我们对XIAP缺陷认识的演变。

Front Pediatr. 2021 Jun 17;9:660520. doi: 10.3389/fped.2021.660520. eCollection 2021.

2

Improved transplant outcomes with myeloablative conditioning for hemophagocytic lymphohistiocytosis in HLA-matched and mismatched donors: a national multicenter retrospective study.异基因造血干细胞移植治疗 HLA 匹配和不匹配供者噬血细胞性淋巴组织细胞增生症的强化预处理方案：一项全国多中心回顾性研究。

Bone Marrow Transplant. 2021 Sep;56(9):2088-2096. doi: 10.1038/s41409-021-01290-1. Epub 2021 Apr 12.

3

Eosinophilic colitis in a boy with a novel XIAP mutation: a case report.

本文引用的文献

1

Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis.以三氟胸苷为基础的儿童和青少年噬血细胞性淋巴组织细胞增生症的预处理方案。

Haematologica. 2014 Jan;99(1):180-4. doi: 10.3324/haematol.2013.094730. Epub 2013 Oct 25.

2

Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.XIAP 缺陷的异基因造血细胞移植：国际调查显示预后不良。

Blood. 2013 Feb 7;121(6):877-83. doi: 10.1182/blood-2012-06-432500. Epub 2012 Nov 6.

3

Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation.