Suppr超能文献

宿主遗传学与结核病:基因多态性与结核病理论

Host genetics and tuberculosis: Theory of genetic polymorphism and tuberculosis.

作者信息

Aravindan P P

机构信息

Former Addl. DHS, Kerala Health Services, Palakkad, Kerala, India.

出版信息

Lung India. 2019 May-Jun;36(3):244-252. doi: 10.4103/lungindia.lungindia_146_15.

Abstract

BACKGROUND AND OBJECTIVE

Tuberculosis (TB), the leading cause of morbidity and mortality by a single infectious agent, Mycobacterium tuberculosis, is still a major health problem in the world. To date, many studies have shown evidence of association between host genetic polymorphisms and TB susceptibility, including chemokine (C-C motif) ligand 2 (CCL-2)/monocyte chemoattractant protein1 (MCP-1), natural resistance-associated macrophage protein 1 (NRAMP-1)/solute carrier protein 11A1 (SLC11A1), Immunity-related GTPase family M protein (IRGMI), interleukin (IL)-8, toll-like receptor (TLR), and nucleotide-binding oligomerization domain containing protein-2 (NOD-2) genes. Most of these genes participate in immune response, and their polymorphism can alter immunity and lead to genetic susceptibility to TB.

MATERIALS AND METHODS

This is a special article compiled with reference to various case-control studies, meta-analysis, and other research work on different genes and TB. The genes selected and a number of studies from different countries and ethnic groups for this article are shown below. The genes selected for the study are: NRAMP-1 (SLC11 A1), Vitamin D receptor, low molecular weight polypeptide/transporter with antigen processing, CCL-2/MCP-1, IRGM-1, IL-1, IL-8, IL-10, IL-12, TLR, NOD-2, human leukocyte antigen, mannose-binding lectin, major histocompatibility complex, tumor necrosis factor, P2X 7, epiregulin, SP110, and interferon gamma (IFN-gamma).

RESULTS

Genetic polymorphisms in different genes showed variable levels of significance in relation to TB. All these were proved by the researchers using appropriate statistical methods and tools.

CONCLUSIONS

Based on different research works across the world, there is sufficient evidence to prove that TB is a genetically primed and determined infectious disease caused by M. tuberculosis and the genetic polymorphism is the mechanism that leads to progression from infection to TB disease. Why only 10-15% of the people infected with M. tuberculosis progress toward TB disease has continued to be an unresolved debate. Hence, for provoking thoughts and encouraging more research in the field of genetics and TB I formulated hypothesis and algorithms, and theory. Genetic susceptibility to TB has been substantiated based on the extensive literature review and the research findings that are well narrated.

摘要

背景与目的

结核病(TB)是由单一感染因子结核分枝杆菌导致发病和死亡的主要原因,至今仍是全球的一个重大健康问题。迄今为止,许多研究已表明宿主基因多态性与结核病易感性之间存在关联证据,包括趋化因子(C-C基序)配体2(CCL-2)/单核细胞趋化蛋白1(MCP-1)、天然抗性相关巨噬细胞蛋白1(NRAMP-1)/溶质载体蛋白11A1(SLC11A1)、免疫相关GTP酶家族M蛋白(IRGMI)、白细胞介素(IL)-8、Toll样受体(TLR)以及含核苷酸结合寡聚化结构域蛋白-2(NOD-2)基因。这些基因大多参与免疫反应,其多态性可改变免疫力并导致对结核病的遗传易感性。

材料与方法

本文是一篇参考了关于不同基因与结核病的各类病例对照研究、荟萃分析及其他研究工作编撰而成的专题文章。以下展示了为本文所选的基因以及来自不同国家和种族的多项研究。所选用于研究的基因包括:NRAMP-1(SLC11A1)、维生素D受体、具有抗原加工功能的低分子量多肽/转运体、CCL-2/MCP-1、IRGM-1、IL-1、IL-8、IL-10、IL-12、TLR、NOD-2、人类白细胞抗原、甘露糖结合凝集素、主要组织相容性复合体、肿瘤坏死因子、P2X7、表皮调节素、SP110以及干扰素γ(IFN-γ)。

结果

不同基因中的遗传多态性在结核病方面显示出不同程度的显著性。研究人员使用适当的统计方法和工具证实了所有这些结果。

结论

基于全球不同的研究工作,有充分证据证明结核病是一种由结核分枝杆菌引发且由基因决定的传染病,而基因多态性是导致从感染发展为结核病的机制。为何只有10% - 15%的结核分枝杆菌感染者会发展为结核病仍是一个未解决的争议。因此,为引发思考并鼓励在遗传学与结核病领域开展更多研究,我提出了假设、算法及理论。基于广泛的文献综述和详细叙述的研究结果,结核病的遗传易感性已得到证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/616e/6503728/fe9af7134936/LI-36-244-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验