Immunological depiction of synthetic B-cell epitopes of Mycobacterium tuberculosis.

IF 1.6 Q4 INFECTIOUS DISEASES
Niharika Sharma, Vishal Khandelwal, S Kumar, B Joshi, Keshar Kunja Mohanty
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引用次数: 0

Abstract

Background: To combat the tuberculosis (TB) epidemic, the development of a better and faster diagnosis or more effective vaccine is essential. Pulmonary TB (PTB) is one of the major causes of morbidity and mortality. Early diagnosis of TB is difficult. Serological assays have been performed with several antigens of laboratory strains such as Mycobacterium tuberculosis H37Rv which have not been found to be highly sensitive. In the present study, various peptides were synthesized which were predicted on the basis of immunoreactivity and differential expression in clinical isolates of M. tuberculosis compared to their expression in a laboratory strain of M. tuberculosis. Therefore, the aim of this study was to compare the antibody levels in PTB and healthy controls against these peptides.

Methods: An effort was made to evaluate antibody response to peptides derived from proteins Rv2588c, Rv0512, Rv0148, Rv0896, and Rv0635 of M. tuberculosis in PTB patients and healthy individuals through enzyme-linked immunosorbent assay. Five milliliters of venous blood samples was collected from each participant, and serum was separated and stored until use.

Results: Antibody levels against these peptides, Rv2588c, Rv0512, Rv0148, Rv0896. and Rv0635 in 139 PTB patients and 52 healthy controls were evaluated. Higher immune response was observed in PTB patients when compared with healthy individuals. Strong immunoglobulin G responses with high percentage, considerable difference among patients and healthy controls was observed with P < 0.0001.

Conclusion: In our study, we found significant statistical differences in antibody levels in PTB patients and healthy individuals against these peptides. These peptides are suggestive of being a potential new candidate (s) for early diagnosis of TB.

结核分枝杆菌合成 B 细胞表位的免疫学描述。
背景:为遏制结核病(TB)的流行,必须开发出更好、更快的诊断方法或更有效的疫苗。肺结核(PTB)是发病和死亡的主要原因之一。结核病的早期诊断十分困难。目前已利用实验室菌株(如结核分枝杆菌 H37Rv)的几种抗原进行了血清学检测,但发现灵敏度并不高。在本研究中,根据结核分枝杆菌临床分离株中的免疫活性和不同表达方式,合成了各种肽,并与结核分枝杆菌实验室菌株中的表达方式进行了比较。因此,本研究的目的是比较 PTB 和健康对照组针对这些肽的抗体水平:方法:通过酶联免疫吸附试验评估 PTB 患者和健康人对来自结核杆菌蛋白 Rv2588c、Rv0512、Rv0148、Rv0896 和 Rv0635 的肽的抗体反应。每位受试者采集五毫升静脉血样本,分离血清并保存至使用:结果:评估了 139 名肺结核患者和 52 名健康对照者针对 Rv2588c、Rv0512、Rv0148、Rv0896 和 Rv0635 这些肽的抗体水平。与健康人相比,肺结核患者的免疫反应更高。患者和健康对照组的免疫球蛋白 G 反应强烈,百分比高,差异显著,P < 0.0001:在我们的研究中,我们发现肺结核患者和健康人对这些肽的抗体水平存在明显的统计学差异。这些肽可作为结核病早期诊断的潜在新候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.20
自引率
25.00%
发文量
62
审稿时长
7 weeks
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