对多疱性麻风病人和家庭接触者的天然抵抗力相关巨噬细胞蛋白1基因表达和抗PGL-1抗体进行比较分析。

E Srihartati, I Agusni, Y Listiawan
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引用次数: 0

摘要

麻风病继续对公共卫生构成重大挑战,尤其是在全球某些地区。准确诊断和了解麻风病的病因对于有效管理和预防麻风病至关重要。本研究旨在探讨自然抗性相关巨噬细胞蛋白1(NRAMP1)及其基因变异以及抗PGL-1抗体水平对患者及其家庭接触者多脓疱型麻风病病理的影响。研究对象包括23名多荫麻风病人和28名家庭接触者。采用 PCR 和 ELISA 技术分别测定了 NRAMP1 蛋白表达、抗-PGL-1 IgG 和 IgM 水平。此外,还检测了 NRAMP1 基因的基因型变异。对数据进行了统计分析,包括曼-惠特尼检验和单变量逻辑回归。在患者组和家庭接触组之间,NRAMP1 蛋白表达以及 IgG 和 IgM 水平存在显著差异。研究还强调了 NRAMP1 基因及其 D543N 和 3'UTR 多态性在麻风病易感性中的作用。两组患者的 INT4 基因型变异无明显差异。这些发现强调了将 PCR 技术与血清学检测相结合以提高麻风病诊断精确度的潜力。这些发现还表明,有必要开展进一步研究,以明确NRAMP1及其多态性在麻风病易感性和耐药性中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative analysis of natural resistance-associated macrophage protein 1 gene expression and anti-PGL-1 antibodies in multibacillary leprosy and household contacts.

Leprosy continues to pose a significant challenge to public health, particularly in certain global regions. Accurate diagnosis and understanding of the disease's etiology are crucial for effective management and prevention. This study aimed to explore the contribution of Natural resistance-associated macrophage protein 1 (NRAMP1) and its genetic variations, as well as the levels of anti-PGL-1 antibodies, to the pathology of multibacillary leprosy in affected individuals and their household contacts. The study included 23 multibacillary leprosy patients and 28 household contacts. NRAMP1 protein expression and anti-PGL-1 IgG and IgM levels were measured using PCR and ELISA techniques, respectively. Genotypic variants of the NRAMP1 gene were also examined. Statistical analyses, including Mann-Whitney tests and univariate logistic regression, were employed to evaluate the data. Significant differences were observed in NRAMP1 protein expression and IgG and IgM levels between the patient and household contact groups. The study also highlighted the role of the NRAMP1 gene and its D543N and 3'UTR polymorphisms in leprosy susceptibility. No significant differences were observed in the genotype variants of INT4 between the two groups. These findings emphasize the potential of integrating PCR technology with serological tests to enhance diagnostic precision in leprosy. They also suggest the need for further research to clarify the role of NRAMP1 and its polymorphisms in leprosy susceptibility and resistance.

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