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Association of Interleukin-10 Cytokine Expression Status with HLA Non-DRB1*02 and Mycobacterium bovis BCG Scar-Negative Status in South Indian Pulmonary Tuberculosis Patients

机译:白细胞介素10细胞因子表达状态与HLA Non-DRB1 * 02和牛分枝杆菌BCG瘢痕阴性状态在南印度肺结核患者中的关联。

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摘要

HLA DRB1*02 and its subtypes predispose individuals for a far-advanced sputum-positive pulmonary tuberculosis transcending ethnic boundaries. Mycobacterium bovis BCG does not afford the desired protection against adult pulmonary tuberculosis, and a spectrum of immune reactivity exists in controls and hospital contacts. All of these findings have been identified and demonstrated in areas of endemicity. Skewing of immunity from protective to pathogenic may involve a shift in the Th1-Th2 paradigm. To elaborate these ideas, we studied gamma interferon (IFN-γ), interleukin-4 (IL-4), and IL-10 cytokine expression in 71 adult pulmonary tuberculosis patients and 74 controls from areas of endemicity in south India by 48-h microculture and reverse transcription-PCR. Most of the patients and controls expressed IFN-γ de novo, and in the presence of purified protein derivative (PPD), all of them expressed significantly higher levels of IFN-γ, suggesting a PPD-specific recall memory. HLA DRB1* allele-dependent IFN-γ expression was identified only in controls, suggesting a skewing of the immune response in patients. In contrast to the case for IFN-γ, only some patients and controls expressed IL-4 or IL-10 (Th2 profile); thus, the Th1 profile was identifiable only by a nonexpression of IL-4 or IL-10 in this area of endemicity. The Th2 profile was associated with HLA non-DRB1*02 and BCG scar-negative status in patients, attributing a significant risk (odds ratio = 2.074; 95% confidence interval = 0.612 to 7.07). It is possible that Mycobacterium tuberculosis (PPD)-specific IL-10 is expressed preemptively in unvaccinated (BCG scar-negative) individuals with a non-DR2 genetic background by chronic exposure in this area of endemicity and leads to pulmonary tuberculosis of adults.
机译:HLA DRB1 * 02及其亚型使个体倾向于超越种族界限的先进的痰阳性肺结核。牛分枝杆菌BCG无法提供所需的抗成人肺结核的保护,对照和医院接触者中存在多种免疫反应性。所有这些发现均已在流行地区得到确认和证明。从保护性免疫转向致病性免疫可能涉及Th1-Th2范式的转变。为了阐明这些想法,我们研究了印度南部地区71名成人肺结核患者和74名来自地方病地区的对照在48小时内的γ干扰素(IFN-γ),白介素4(IL-4)和IL-10细胞因子的表达。微培养和逆转录PCR。大多数患者和对照从头表达IFN-γ,并且在存在纯化的蛋白衍生物(PPD)的情况下,他们所有人均表达明显更高的IFN-γ水平,这表明PPD特异性召回记忆。仅在对照组中发现了HLA DRB1 *等位基因依赖性IFN-γ表达,提示患者的免疫应答有偏斜。与IFN-γ的情况相反,只有部分患者和对照组表达IL-4或IL-10(Th2谱)。因此,仅通过在该流行地区不表达IL-4或IL-10才能鉴定Th1分布。 Th2谱与患者的HLA非DRB1 * 02和BCG瘢痕阴性相关,并具有显着风险(赔率= 2.074; 95%置信区间= 0.612至7.07)。结核分枝杆菌(PPD)特异性IL-10可能通过在该地方病地区的长期暴露而在具有非DR2遗传背景的未接种疫苗的人群中(BCG疤痕阴性)抢先表达,并导致成年人的肺结核。

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