Hammrich Judith, Wittig Susan, Ernst Thomas, Gruhn Bernd
Department of Pediatrics, Jena University Hospital, Am Klinikum 1, 07747, Jena, Germany.
Department of Internal Medicine Il, Jena University Hospital, Jena, Germany.
J Cancer Res Clin Oncol. 2018 Mar;144(3):587-592. doi: 10.1007/s00432-018-2578-8. Epub 2018 Jan 15.
Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative approach for a variety of hematological diseases; however, it is still associated with substantial morbidity and mortality. Transplant-related mortality (TRM) after HSCT depends mainly on the toxicity of the conditioning regimen, infections, and graft-versus-host disease. The purpose of this study was to identify the association between CTLA-4 single nucleotide polymorphisms and TRM in children undergoing allogeneic HSCT.
153 donors and 153 children with acute lymphoblastic leukemia, acute myeloid leukemia or juvenile myelomonocytic leukemia who had undergone allogeneic HSCT were genotyped of CTLA-4 gene for rs3087243 (CT60G>A), rs231775 (+ 49 A>G) and rs4553808 using TaqMan real-time polymerase chain reaction.
We observed a significant association between the donor's CLTA-4 genotype of rs3087243 and TRM in children undergoing allogeneic HSCT. Genotype AG was found in 78 donors (51%), GG in 44 donors (29%) and 31 donors (20%) were homozygous for AA. 30 patients died as a result of transplant-related causes. Interestingly, we observed a significantly reduced TRM in children who were transplanted from a donor with the CTLA-4 genotype GG in comparison to genotype AG or AA (9 versus 19 versus 36%, P = 0.013). In addition, we found significant differences of event-free survival (EFS) depending on the donor's genotype. The EFS was 64, 46 or 32% if the patient was transplanted from a donor with CTLA-4 genotype GG, AG or AA, respectively (P = 0.043). In multivariate analysis, CTLA-4 genotype of rs3087243 was an independent risk factor for TRM (P = 0.011) and EFS (P = 0.035).
This study provides first evidence that the CTLA-4 polymorphisms are significant risk factors for TRM and survival in children undergoing allogeneic HSCT and should be evaluated in further trials.
异基因造血干细胞移植(HSCT)是治疗多种血液疾病的有效方法;然而,它仍与较高的发病率和死亡率相关。HSCT后的移植相关死亡率(TRM)主要取决于预处理方案的毒性、感染和移植物抗宿主病。本研究的目的是确定接受异基因HSCT的儿童中CTLA-4单核苷酸多态性与TRM之间的关联。
对153名供者以及153名接受异基因HSCT的急性淋巴细胞白血病、急性髓细胞白血病或青少年粒单核细胞白血病患儿进行CTLA-4基因rs3087243(CT60G>A)、rs231775(+49 A>G)和rs4553808的基因分型,采用TaqMan实时聚合酶链反应。
我们观察到供者rs3087243的CLTA-4基因型与接受异基因HSCT的儿童的TRM之间存在显著关联。78名供者(51%)为AG基因型,44名供者(29%)为GG基因型,31名供者(20%)为AA纯合子。30例患者死于移植相关原因。有趣的是,我们观察到与AG或AA基因型相比,接受CTLA-4基因型为GG的供者移植的儿童TRM显著降低(分别为9%、19%和36%,P = 0.013)。此外,我们发现根据供者基因型,无事件生存期(EFS)存在显著差异。如果患者接受CTLA-4基因型为GG、AG或AA的供者移植,EFS分别为64%、46%或32%(P = 0.043)。在多变量分析中,rs3087243的CTLA-4基因型是TRM(P = 0.011)和EFS(P = 0.035)的独立危险因素。
本研究首次提供证据表明,CTLA-4多态性是接受异基因HSCT的儿童TRM和生存的重要危险因素,应在进一步试验中进行评估。