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Association of ABCB1 gene polymorphisms and haplotypes with therapeutic efficacy of glucocorticoids in Chinese patients with immune thrombocytopenia

机译:中国免疫性血小板减少症患者ABCB1基因多态性和单倍型与糖皮质激素治疗疗效的关系

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摘要

Resistance to glucocorticoids (GCs) remains a tricky problem complicating the therapy of ITP. Recently, ATP binding cassette gene B1 gene (ABCB1) was reported to be correlated with susceptibility and therapeutic efficacy of autoimmune diseases through P-glycoprotein (Pgp). We investigated three single nucleotide polymorphisms (SNPs) of ABCB1 and their haplotypes by PCR-RFLP (restriction fragment length polymorphism) method in 471 ITP patients and 383 healthy controls, patients were further assigned into GCs-responsive and -non-responsive group according to the therapeutic effects of GCs. We observed a remarkable difference in genotypes of G2677T/A between GCs-responsive and non-responsive group, but not between patients and controls. A frequently expression of T/A allele within G2677T/A was recorded in GCs-responsive group. Furthermore, we found that some haplotypes (CGC, CTC/CAC, CTT/CAT, TGC, TGT, TTC/TAC and TTT/TAT, in the order of position 1236-2677-3435) were presented significantly differences between non-responsive and responsive group. No difference of C1236T and C3435T polymorphisms was observed between ITP and controls, and between the GCs-responsive and -non-responsive group. Our findings suggest that ABCB1 polymorphisms, as well as haplotypes derived from C1235T, G2677T/A and C3435T, are associated with inter-individual differences of GCs treatment in ITP.
机译:对糖皮质激素(GCs)的耐药性仍然是棘手的问题,使ITP的治疗复杂化。最近,据报道ATP结合盒基因B1基因(ABCB1)与通过P-糖蛋白(Pgp)自身免疫性疾病的易感性和治疗功效相关。我们通过PCR-RFLP(限制性片段长度多态性)方法研究了471名ITP患者和383名健康对照者的ABCB1的三个单核苷酸多态性(SNP)及其单倍型,根据这些患者进一步分为GCs应答和-非应答组气相色谱的治疗效果。我们观察到GCs反应组和非反应组之间G2677T / A的基因型有显着差异,但患者和对照组之间没有差异。 GCs响应组记录了G2677T / A中T / A等位基因的频繁表达。此外,我们发现一些单倍型(CGC,CTC / CAC,CTT / CAT,TGC,TGT,TTC / TAC和TTT / TAT,按位置1236-2677-3435的顺序)表现出无反应型和单反应型之间的显着差异。响应组。在ITP和对照组之间以及在GCs反应组和-non-response组之间,没有观察到C1236T和C3435T多态性的差异。我们的发现表明,ABCB1多态性以及源自C1235T,G2677T / A和C3435T的单倍型与ITP中GC治疗的个体差异有关。

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