Department of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar, Punjab, India.
Int J Tuberc Lung Dis. 2010 Sep;14(9):1159-63.
Development of tuberculosis (TB) disease is an outcome of complex host-pathogen interactions. The purinergic P2X(7) receptors are adenosine triphosphate gated molecules shown to induce killing of intracellular Mycobacterium tuberculosis, followed by apoptosis of the infected macrophage. A single nucleotide polymorphism in exon 13 of the P2X(7) receptors gene at +1513 position has been shown to abolish the function of this receptor and to be associated with increased susceptibility to TB in some ethnic groups.
To explore the association of +1513 (A-->C) polymorphism in TB patients in Punjab, North India.
A case-control study was conducted by studying peripheral blood samples from 204 TB patients (181 pulmonary, 23 extra-pulmonary) and 177 controls with no history of TB. P2X(7) +1513 (A-->C) polymorphism was studied using amplification refractory mutation system analysis.
The distribution of +1513 A/C genotypes in the TB patient and the control groups revealed a statistically significant association with TB (P = 0.002).
The +1513C allele is a risk factor for the development of TB in the North Indian Punjabi population.
结核病(TB)的发展是宿主-病原体相互作用的复杂结果。嘌呤能 P2X(7)受体是三磷酸腺苷门控分子,已被证明可诱导细胞内结核分枝杆菌的杀伤,随后感染的巨噬细胞发生凋亡。已发现 P2X(7)受体基因第 13 外显子在 +1513 位的单核苷酸多态性可使该受体丧失功能,并与某些族群中结核病的易感性增加有关。
探讨印度旁遮普邦结核病患者中+1513(A-->C)多态性的相关性。
通过研究 204 例结核病患者(181 例肺部,23 例肺外)和 177 例无结核病史的对照者的外周血样本进行病例对照研究。采用扩增受阻突变系统分析研究 P2X(7)+1513(A-->C)多态性。
TB 患者和对照组中+1513A/C 基因型的分布与 TB 存在统计学显著关联(P=0.002)。
+1513C 等位基因是印度旁遮普邦人群发生结核病的危险因素。