Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
BMC Med Genet. 2011 Dec 15;12:162. doi: 10.1186/1471-2350-12-162.
IL8RA and IL8RB, encoded by CXCR1 and CXCR2, are receptors for interleukin (IL)-8 and other CXC chemokines involved in chemotaxis and activation of polymorphonuclear neutrophils (PMN). Variants at CXCR1 and CXCR2 have been associated with susceptibility to cutaneous and mucocutaneous leishmaniasis in Brazil. Here we investigate the role of CXCR1/CXCR2 in visceral leishmaniasis (VL) in India.
Three single nucleotide polymorphisms (SNPs) (rs4674259, rs2234671, rs3138060) that tag linkage disequilibrium blocks across CXCR1/CXCR2 were genotyped in primary family-based (313 cases; 176 nuclear families; 836 individuals) and replication (941 cases; 992 controls) samples. Family- and population-based analyses were performed to look for association between CXCR1/CXCR2 variants and VL. Quantitative RT/PCR was used to compare CXCR1/CXCR2 expression in mRNA from paired splenic aspirates taken before and after treatment from 19 VL patients.
Family-based analysis using FBAT showed association between VL and SNPs CXCR1_rs2234671 (Z-score = 2.935, P = 0.003) and CXCR1_rs3138060 (Z-score = 2.22, P = 0.026), but not with CXCR2_rs4674259. Logistic regression analysis of the case-control data under an additive model of inheritance showed association between VL and SNPs CXCR2_rs4674259 (OR = 1.15, 95%CI = 1.01-1.31, P = 0.027) and CXCR1_rs3138060 (OR = 1.25, 95%CI = 1.02-1.53, P = 0.028), but not with CXCR1_rs2234671. The 3-locus haplotype T_G_C across these SNPs was shown to be the risk haplotype in both family- (TRANSMIT; P = 0.014) and population- (OR = 1.16, P = 0.028) samples (combined P = 0.002). CXCR2, but not CXCR1, expression was down regulated in pre-treatment compared to post-treatment splenic aspirates (P = 0.021).
This well-powered primary and replication genetic study, together with functional analysis of gene expression, implicate CXCR2 in determining outcome of VL in India.
IL8RA 和 IL8RB 由 CXCR1 和 CXCR2 编码,是白细胞介素 (IL)-8 和其他 CXC 趋化因子的受体,参与趋化和多形核粒细胞 (PMN) 的激活。CXCR1 和 CXCR2 上的变体与巴西皮肤和粘膜利什曼病的易感性有关。在这里,我们研究了 CXCR1/CXCR2 在印度内脏利什曼病 (VL) 中的作用。
在原发性基于家庭的 (313 例;176 个核家庭;836 人) 和复制 (941 例;992 例对照) 样本中,对 CXCR1/CXCR2 上标记连锁不平衡块的三个单核苷酸多态性 (SNP) (rs4674259、rs2234671、rs3138060) 进行了基因分型。进行了基于家庭和人群的分析,以寻找 CXCR1/CXCR2 变异与 VL 之间的关联。使用定量 RT/PCR 比较了 19 例 VL 患者治疗前后配对脾抽吸物中 CXCR1/CXCR2 的 mRNA 表达。
FBAT 中的基于家庭的分析显示,VL 与 SNP CXCR1_rs2234671 (Z 分数 = 2.935,P = 0.003) 和 CXCR1_rs3138060 (Z 分数 = 2.22,P = 0.026) 之间存在关联,但与 CXCR2_rs4674259 无关。在遗传加性模型下对病例对照数据的逻辑回归分析显示,VL 与 SNP CXCR2_rs4674259 (OR = 1.15,95%CI = 1.01-1.31,P = 0.027) 和 CXCR1_rs3138060 (OR = 1.25,95%CI = 1.02-1.53,P = 0.028) 之间存在关联,但与 CXCR1_rs2234671 无关。这些 SNP 之间的 3 个单核苷酸多态性 T_G_C 被证明是家庭 (TRANSMIT;P = 0.014) 和人群 (OR = 1.16,P = 0.028) 样本中的风险单倍型 (合并 P = 0.002)。与治疗前相比,治疗后脾抽吸物中 CXCR2 而非 CXCR1 的表达下调 (P = 0.021)。
这项经过充分验证的原发性和复制遗传研究,以及对基因表达的功能分析,提示 CXCR2 在决定印度 VL 的结局方面起作用。