Hoh B P, Umi-Shakina H, Zuraihan Z, Zaiharina M Z, Rafidah-Hanim S, Mahiran M, Khairudin N Y Nik, Benedict L H Sim, Masliza Z, Christopher K C Lee, Sazaly A B
Institute of Medical Molecular Biotechnology (IMMB), Faculty of Medicine, Universiti Teknologi MARA, Sg Buloh Campus, Jalan Hospital, 47000 Sungai Buloh, Selangor, Malaysia.
Institute of Medical Molecular Biotechnology (IMMB), Faculty of Medicine, Universiti Teknologi MARA, Sg Buloh Campus, Jalan Hospital, 47000 Sungai Buloh, Selangor, Malaysia.
Hum Immunol. 2015 Jun;76(6):421-6. doi: 10.1016/j.humimm.2015.03.019. Epub 2015 Apr 7.
Dengue causes significantly more human disease than any other arboviruses. It causes a spectrum of illness, ranging from mild self-limited fever, to severe and fatal dengue hemorrhagic fever, as evidenced by vascular leakage and multifactorial hemostatic abnormalities. There is no specific treatment available till date. Evidence shows that chemokines CXCL10, CXCL11 and their receptor CXCR3 are involved in severity of dengue, but their genetic association with the susceptibility of vascular leakage during dengue infection has not been reported. We genotyped 14 common variants of these candidate genes in 176 patients infected with dengue. rs4859584 and rs8878 (CXCL10) were significantly associated with vascular permeability of dengue infection (P<0.05); while variants of CXCL11 showed moderate significance of association (P=0.0527). Haplotype blocks were constructed for genes CXCL10 and CXCL11 (5 and 7 common variants respectively). Haplotype association tests performed revealed that, "CCCCA" of gene CXCL10 and "AGTTTAC" of CXCL11 were found to be significantly associated with vascular leakage (P=0.0154 and 0.0366 respectively). In summary, our association study further strengthens the evidence of the involvement of CXCL10 and CXCL11 in the pathogenesis of dengue infection.
登革热导致的人类疾病比任何其他虫媒病毒都要多得多。它会引发一系列疾病,从轻微的自限性发热到严重的、致命的登革出血热,血管渗漏和多因素止血异常就是证明。迄今为止尚无特效治疗方法。有证据表明趋化因子CXCL10、CXCL11及其受体CXCR3与登革热的严重程度有关,但它们与登革热感染期间血管渗漏易感性的基因关联尚未见报道。我们对176例登革热感染患者的这些候选基因的14个常见变异进行了基因分型。rs4859584和rs8878(CXCL10)与登革热感染的血管通透性显著相关(P<0.05);而CXCL11的变异显示出中等程度的关联显著性(P=0.0527)。构建了CXCL10和CXCL11基因的单倍型模块(分别有5个和7个常见变异)。进行的单倍型关联测试显示,发现CXCL10基因的“CCCCA”和CXCL11基因的“AGTTTAC”与血管渗漏显著相关(分别为P=0.0154和0.0366)。总之,我们的关联研究进一步强化了CXCL10和CXCL11参与登革热感染发病机制的证据。