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结核分枝杆菌mce4操纵子的重组LprN蛋白在小鼠中诱导对保护性免疫有害的Th-1型反应。

The Mycobacterium tuberculosis recombinant LprN protein of mce4 operon induces Th-1 type response deleterious to protection in mice.

作者信息

Pasricha Rashmi, Saini Neeraj K, Rathor Nisha, Pathak Rakesh, Sinha Rajesh, Varma-Basil Mandira, Mishra Kiran, Brahmachari Vani, Bose Mridula

机构信息

Department of Microbiology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, India.

出版信息

Pathog Dis. 2014 Dec;72(3):188-96. doi: 10.1111/2049-632X.12200. Epub 2014 Aug 7.

Abstract

Lipoproteins are known to be effective immunogens and affect both innate and adaptive immunity. The lprN gene of Mycobacterium tuberculosis has been predicted to encode for a putative lipoprotein in silico. Here, we studied its function as an immunogen by in vivo studies in mice. The recombinant LprN protein, expressed and purified in Escherichia coli, triggered a cell-mediated immune response in BALB/c mice. This was observed by significantly higher T-cell proliferation and increased production of TNF-α and IFN-γ cytokines. However, pre-exposure to LprN protein failed to provide protection in mice after challenge with a virulent strain of M. tuberculosis. Histological examination showed an increase in tissue destruction in experimental animals, indicating an immunogenic potential for LprN protein that enhanced the virulence of bacilli.

摘要

众所周知,脂蛋白是有效的免疫原,会影响先天性免疫和适应性免疫。结核分枝杆菌的lprN基因在计算机模拟中被预测编码一种假定的脂蛋白。在此,我们通过在小鼠体内进行的研究来探究其作为免疫原的功能。在大肠杆菌中表达并纯化的重组LprN蛋白在BALB/c小鼠中引发了细胞介导的免疫反应。这可通过显著更高的T细胞增殖以及肿瘤坏死因子-α和干扰素-γ细胞因子产量增加得以观察到。然而,在感染强毒株结核分枝杆菌之前预先接触LprN蛋白未能为小鼠提供保护。组织学检查显示实验动物的组织破坏增加,表明LprN蛋白具有增强杆菌毒力的免疫原性潜力。

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