Polymorphism in the interleukin-10 gene is associated with overactive bladder phenotype associated with HTLV-1 infection
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Abstract INTRODUCTION Human T-cell lymphotropic virus type 1 (HTLV-1)-associated inflammatory diseases are not well understood; however, their clinical manifestations may be influenced by the host genetic background. METHODS We genotyped 298 individuals with HTLV-1 and 380 controls for interleukin-10 (IL10) gene variants-rs3024496, rs1800871, rs1800896-and used logistic regression analysis to determine their association with clinical phenotypes. RESULTS No association with HTLV-1 infection was observed. However, allele A of rs1800896 (1082bp upstream) was associated with protection against neurological impairment, specifically overactive bladder (OR=0.447, 95% CI 0.28-0.70, p=0.001). CONCLUSIONS Our data suggests that IL10 regulation ameliorates neurological damage in HTLV-1 infections.
摘要 引言:人类T细胞嗜淋巴病毒1型(HTLV-1)相关炎症性疾病的致病机制尚未完全阐明,但其临床表现可能受宿主遗传背景影响。 方法:本研究对298名HTLV-1感染者及380名健康对照者的白细胞介素-10(IL10)基因的rs3024496、rs1800871、rs1800896三个变异位点进行基因分型,并采用logistic回归分析探讨其与临床表型的关联。 结果:未观察到上述变异位点与HTLV-1感染存在关联。但rs1800896(位于转录起始位点上游1082bp处)的A等位基因可对神经功能损害起到保护作用,尤其是针对膀胱过度活动症(OR=0.447, 95% CI 0.28-0.70, p=0.001)。 结论:本研究数据表明,IL10的调控可减轻HTLV-1感染引发的神经损伤。



