Development of a novel anti ESAT-6 monoclonal antibody for screening of Mycobacterium tuberculosis

被引:0
作者
Leng, Jianhang [1 ]
Ding, Yu [1 ]
Shou, Chengmin [2 ]
Wu, Zhigang [3 ]
Zhuo, Guangchao [1 ]
Wang, Keyi [1 ]
Shen, Junya [1 ]
Huang, Sheng [4 ]
机构
[1] Nanjing Med Univ, Affiliated Hangzhou Hosp, Hangzhou Peoples Hosp 1, Cent Lab, Hangzhou 310006, Zhejiang, Peoples R China
[2] Red Cross Hosp Hangzhou, Dept Endocrinol, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[4] Nanjing Med Univ, Affiliated Hangzhou Hosp, Hangzhou Peoples Hosp 1, Dept Pneumol, Hangzhou 310006, Zhejiang, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2014年 / 7卷 / 11期
关键词
Anti-ESAT-6; monoclonal antibody; immunological detection; Mycobacterium tuberculosis; DIAGNOSIS; BCG; PROTEINS; VACCINES; COMPLEX; GENOME; REGION; CFP-10;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tuberculosis (TB) is a major global public health problem with an estimated one-third of the world's population infected with Mycobacterium tuberculosis, thus necessitating fast and accurate diagnosis of TB. However, the diagnosis of latent infection remains difficult due to the lack of a simple, reliable test for M. tuberculosis infection. The objective of the current study was to generate and characterize a novel monoclonal antibody (mAb) that specifically target the early secretory antigenic target 6 (ESAT-6) protein for tuberculosis (TB) immunological diagnosis. The BALB/c mice were immunized by a peptide with 13 amino acids (amino acid residues 24 to 36) of ESAT-6 protein. Stable hybridomas cell lines were established and mAb was identified by Western Blot, immunoprecipitation (IP) and Enzyme linked immunosorbent assay (ELISA). In addition, this mouse mAb was used to coat plates, and biotin-labelled polyclonal antibodies were used to detect the antigens. Finally, the antibody was verified in 280 patient sputum culture supernatants and pleural effusion aspirates. The positive detection rate of the generated ESAT-6 mAb was 91% in the clinical diagnosis of tuberculosis pleural effusion, and this mAb had a sensitivity of 92.4% and a specificity of 100% in all M. tuberculosis cases. Our data indicated that the mAb generated in this study can potentially serve as a tool in the laboratory diagnosis of TB.
引用
收藏
页码:4238 / 4243
页数:6
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