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Increased incidence of autoimmune cytopenias after allogeneic haematopoietic stem cell transplantation using a matched unrelated donor in children with β-thalassaemia.

作者信息

Oikonomopoulou Christina, Paisiou Anna, Komitopoulou Anna, Ioannidou Eleni-Dikaia, Kaisari Aikaterini, Tzannou Ifigeneia, Mpourazani Evdoxia, Vessalas George, Peristeri Ioulia, Kitra-Roussou Vassiliki, Goussetis Evgenios

机构信息

Stem Cell Transplant Unit, Aghia Sophia Children's Hospital, Athens, Greece.

Pediatric Intensive Care Unit, Aghia Sophia Children's Hospital, Athens, Greece.

出版信息

Br J Haematol. 2021 Mar;192(5):e127-e129. doi: 10.1111/bjh.17335. Epub 2021 Feb 1.

DOI:10.1111/bjh.17335
PMID:33522599
Abstract
摘要

相似文献

1
Increased incidence of autoimmune cytopenias after allogeneic haematopoietic stem cell transplantation using a matched unrelated donor in children with β-thalassaemia.在β地中海贫血患儿中，使用匹配的无关供体进行异基因造血干细胞移植后自身免疫性血细胞减少症的发病率增加。
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2
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Posttransplant autoimmune hemolytic anemia and other autoimmune cytopenias are increased in very young infants undergoing unrelated donor umbilical cord blood transplantation.接受非亲属供者脐血移植的小婴儿发生移植后自身免疫性溶血性贫血和其他自身免疫性血细胞减少症的情况有所增加。
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Alternative Donor/Unrelated Donor Transplants for the β-Thalassemia and Sickle Cell Disease.β地中海贫血和镰状细胞病的替代供体/非亲属供体移植
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Unrelated Donor Peripheral Blood Stem Cell Transplantation for Patients with β-Thalassemia Major Based on a Novel Conditioning Regimen.基于新型预处理方案的重型β地中海贫血患者无关供体外周血造血干细胞移植。
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Rapid and complete donor chimerism after unrelated mismatched cord blood transplantation in 5 children with beta-thalassemia major.5例重型β地中海贫血患儿接受非亲缘脐血不匹配移植后快速且完全的供者嵌合状态
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An immunological syndrome featuring transverse myelitis, Evans syndrome and pulmonary infiltrates after unrelated bone marrow transplant in a patient with severe aplastic anemia.一名重型再生障碍性贫血患者在接受非亲缘骨髓移植后出现以横贯性脊髓炎、伊文氏综合征和肺部浸润为特征的免疫综合征。
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引用本文的文献

1
Advancing the care of β-thalassaemia patients with novel therapies.推进新型疗法治疗β-地中海贫血患者。
Blood Transfus. 2022 Jan;20(1):78-88. doi: 10.2450/2021.0265-21. Epub 2021 Oct 21.
2
HSCT remains the only cure for patients with transfusion-dependent thalassemia until gene therapy strategies are proven to be safe.异基因造血干细胞移植仍然是输血依赖型地中海贫血患者的唯一治愈方法，直到基因治疗策略被证明是安全的。
Bone Marrow Transplant. 2021 Dec;56(12):2882-2888. doi: 10.1038/s41409-021-01461-0. Epub 2021 Sep 16.