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Association of the costimulatory molecule gene polymorphisms and active cytomegalovirus infection in hematopoietic stem cell transplant patients

机译:共刺激分子基因多态性与造血干细胞移植患者活动性巨细胞病毒感染的关系

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Determinative associations may exist between costimulatory molecule gene polymorphisms with a variety of post hematopoietic stem cell transplantation (HSCT) viral related clinical outcomes especially acute graft versus host disease (aGVHD). Therefore in this study the associations between costimulatory molecule gene polymorphisms including: cytotoxic T-lymphocyte antigen-4 (CTLA4), programmed cell death-1 (PD-1), inducible T cell costimulator (ICOS), and cluster differentiation 28 (CD28) with active cytomegalovirus (CMV) infection were evaluated in HSCT patients. The 72 allogeneic HSCT patients with and without aGVHD were enrolled in this cross sectional study between years: 2004-2011. The single nucleotide polymorphisms in loci of the costimulatory molecules including: CTLA4 gene (-318 C/T, 1722 T/C, 1661 A/G, +49 A/G), PD-1 gene (PD-1.3 A/G, PD-1.9 C/T), ICOS gene (1720 C/T), and CD28 gene (+17 C/T) were analyzed in studied HSCT patients by PCR-RFLP methods. The active CMV infection was evaluated in fresh EDTA-treated blood samples of each allogeneic HSCT patients by CMV antigenemia kit according to manufacturer's instruction. Active CMV infection was found in 11 of 72 (15.27 %) of allogeneic HSCT patients. The T allele and TT genotype of the CD28 +17 C/T were significantly higher frequency in active CMV infected allogeneic HSCT patients experienced aGVHD. The G allele and GG genotype of the CTLA4 -1661 A/G were significantly higher frequent in active CMV infected allogeneic HSCT patients experienced low grade of aGVHD. Finally, finding of significant associations between CD28 +17 C/T and CTLA4 -1661 A/G genotypes with CMV active infection in allogeneic HSCT patients experienced aGVHD emphasize on the importance of the genetic pattern of costimulatory genes in outcomes of active CMV infection in HSCT patients needs completed studies.
机译:共刺激分子基因多态性与各种造血后干细胞移植(HSCT)病毒相关的临床结果,尤其是急性移植物抗宿主病(aGVHD)之间可能存在确定的关联。因此,在这项研究中,共刺激分子基因多态性之间的关联包括:细胞毒性T淋巴细胞抗原4(CTLA4),程序性细胞死亡1(PD-1),诱导型T细胞共刺激物(ICOS)和簇分化28(CD28)。在HSCT患者中评估了患有活动性巨细胞病毒(CMV)感染的患者。该横断面研究纳入了2004年至2011年之间的72例有或没有aGVHD的异基因HSCT患者。共刺激分子的基因座中的单核苷酸多态性包括:CTLA4基因(-318 C / T,1722 T / C,1661 A / G,+ 49 A / G),PD-1基因(PD-1.3 A / G,通过PCR-RFLP方法对HSCT患者进行PD-1.9 C / T),ICOS基因(1720 C / T)和CD28基因(+17 C / T)分析。通过CMV抗原血症试剂盒,按照制造商的说明,在每个同种异体HSCT患者的新鲜EDTA处理过的血液样本中评估了活性CMV感染。在同种异体HSCT患者中,有72名中的11名(15.27%)发现了主动CMV感染。 CD28 +17 C / T的T等位基因和TT基因型在经历aGVHD的活跃CMV感染同种异体HSCT患者中出现频率更高。在活跃的CMV感染的同种异体HSCT患者中,CTLA4 -1661 A / G的G等位基因和GG基因型显着更高,其aGVHD水平较低。最后,在同种异体HSCT患者中发现CD28 +17 C / T和CTLA4 -1661 A / G基因型与CMV活动感染之间存在显着关联,经历了aGVHD强调在HSCT活动性CMV感染结果中共刺激基因遗传模式的重要性患者需要完成研究。

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