López-Maderuelo Dolores, Arnalich Francisco, Serantes Rocio, González Alicia, Codoceo Rosa, Madero Rosario, Vázquez Juan J, Montiel Carmen
Internal Medicine Service, Hospital La Paz, Maternidad Planta 8, Paseo de la Castellana 241, 28046 Madrid, Spain.
Am J Respir Crit Care Med. 2003 Apr 1;167(7):970-5. doi: 10.1164/rccm.200205-438BC. Epub 2003 Jan 16.
Several genes coding for different cytokines may affect host susceptibility to tuberculosis. This study investigates the relationship of the single base change polymorphic variants identified in the first intron of interferon-gamma (+874 T/A) and in the promoter region of interleukin-10 gene (-1,082 G/A), with cytokine production by peripheral blood mononuclear cells and tuberculosis susceptibility. We studied a Spanish population of 113 patients with culture-proven pulmonary tuberculosis, 207 healthy close contacts (125 tuberculin reactive and 82 tuberculin negative), and 100 healthy tuberculin-negative control subjects. Multiple logistic regression analysis showed that individuals homozygous for the interferon-gamma (+874) A allele had a 3.75-fold increased risk of developing tuberculosis (95% confidence interval, 2.26-6.23, p = 0.0017). Stimulated production of interferon-gamma by peripheral mononuclear cells from patients with genotype AA was depressed compared with that of non-AA homozygotes at the time of diagnosis and after completion of therapy. Multivariate analysis showed that the presence of an AA genotype and the absolute number of lymphocytes were the only independent predictors of interferon-gamma production. In contrast, the different rates of interleukin-10 production associated with the interleukin-10 polymorphism did not affect susceptibility to tuberculosis. Thus, a genetic defect in the production of interferon-gamma in individuals homozygous for the (+874) A allele could contribute to their increased risk of developing tuberculosis.
几个编码不同细胞因子的基因可能会影响宿主对结核病的易感性。本研究调查了在干扰素-γ基因第一内含子(+874 T/A)和白细胞介素-10基因启动子区域(-1,082 G/A)中鉴定出的单碱基变化多态性变体与外周血单核细胞产生细胞因子及结核病易感性之间的关系。我们研究了一个西班牙人群,其中包括113例经培养证实的肺结核患者、207名健康密切接触者(125名结核菌素反应阳性和82名结核菌素反应阴性)以及100名健康结核菌素反应阴性对照者。多因素逻辑回归分析显示,干扰素-γ(+874)A等位基因纯合个体患结核病的风险增加了3.75倍(95%置信区间,2.26 - 6.23,p = 0.0017)。与非AA纯合子相比,基因型为AA的患者外周单核细胞在诊断时和治疗完成后,其干扰素-γ的刺激产生量降低。多变量分析表明,AA基因型的存在和淋巴细胞绝对计数是干扰素-γ产生的唯一独立预测因素。相比之下,与白细胞介素-10多态性相关的白细胞介素-10产生率差异并未影响对结核病的易感性。因此,(+874)A等位基因纯合个体中干扰素-γ产生的遗传缺陷可能导致其患结核病风险增加。