首页> 美国卫生研究院文献>Journal of Hematology Oncology >Conditioning with rabbit versus horse ATG dramatically alters clinical outcomes in identical twins with severe aplastic anemia transplanted with the same allogeneic donor
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Conditioning with rabbit versus horse ATG dramatically alters clinical outcomes in identical twins with severe aplastic anemia transplanted with the same allogeneic donor

机译:兔对马ATG的条件治疗会显着改变同种异体供体移植的严重再生障碍性贫血的同卵双胞胎的临床结果

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摘要

Severe aplastic anemia (SAA) is a rare disorder leading to bone marrow failure, which if left untreated, is invariably fatal. Conventional therapies with immunosuppressive therapy or allogeneic hematopoietic stem cell transplantation (HSCT) are highly effective. HSCT can offer a greater outcome in younger patients who have an available HLA match-related donor. Recent studies showing the addition of antithymocyte globulin (ATG) to the conditioning regimen improves engraftment and reduces the risk of graft-versus-host disease (GVHD).There are currently two ATG preparations in the USA, equine (or horse) and rabbit ATG. These agents are pharmacologically distinct, having significant differences in their pharmacokinetics and in vivo immunosuppressive effects [N Engl J Med 365(5):430–438, 2011]. Here, we report a case of two monozygotic twins with constitutional SAA that evolved to myelodysplastic syndrome (MDS) who both underwent allogeneic peripheral blood stem cell transplantation (PBSC) from the same single HLA antigen mismatched sibling donor with the only difference in the transplant regimen being the type of ATG used in the preparative regimen; one twin received horse ATG and the other received rabbit ATG during conditioning. This report emphasizes that dramatic differences in donor T cell chimerism and clinical outcomes including GVHD can occur as a consequence of the type of ATG that is utilized in the transplant conditioning regimen. These differences highlight that these agents should not be considered interchangeable drugs when used in this setting.
机译:严重再生障碍性贫血(SAA)是导致骨髓衰竭的罕见疾病,如果不及时治疗,肯定会致命。带有免疫抑制疗法或同种异体造血干细胞移植(HSCT)的常规疗法非常有效。 HSCT可以为拥有可用HLA比赛相关供体的年轻患者提供更好的结果。最近的研究表明,在调理方案中添加抗胸腺细胞球蛋白(ATG)可以改善移植并降低移植物抗宿主病(GVHD)的风险。美国目前有两种ATG制剂,马(或马)和兔ATG 。这些药物在药理学上是截然不同的,其药代动力学和体内免疫抑制作用均存在显着差异[N Engl J Med 365(5):430–438,2011]。在这里,我们报道了两个单卵双生双胞胎,其体质SAA演变为骨髓增生异常综合症(MDS),他们均从同一个HLA抗原错配的同胞供体进行了异基因外周血干细胞移植(PBSC),唯一的区别在于移植方案制备方案中使用的ATG类型;一对双胞胎在调节过程中接受了马ATG,另一对接受了兔ATG。该报告强调,由于移植条件疗法中使用的ATG类型的不同,可能会导致供体T细胞嵌合和临床结果(包括GVHD)发生巨大差异。这些差异表明,在这种情况下使用这些药物时,不应将其视为可互换药物。

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