Immune response to Mycobacterium tuberculosis specific antigen ESAT-6 among south Indians

被引:17
作者
Kumar, Madhan [1 ]
Meenakshi, N. [2 ]
Sundaramurthi, Jagadish C. [3 ]
Kaur, Gurvinder [4 ]
Mehra, Narinder K. [4 ]
Raja, Alamelu [1 ]
机构
[1] TB Res Ctr ICMR, Dept Immunol, Madras 600031, Tamil Nadu, India
[2] Govt Thiruvotteeswarar Hosp Thorac Med, Madras 600012, Tamil Nadu, India
[3] TB Res Ctr ICMR, Biomed Informat Ctr, Madras 600031, Tamil Nadu, India
[4] All India Inst Med Sci, Dept Transplant Immunol & Immunogenet, New Delhi, India
关键词
Tuberculosis; ESAT-6; peptides; Vaccines; HLA; 20-mer peptides; T-CELL RESPONSES; ACTIVE PULMONARY TUBERCULOSIS; HEALTHY HOUSEHOLD CONTACTS; INTERFERON-GAMMA; INDUCED PROLIFERATION; CYTOKINE RESPONSES; PLEURAL EFFUSIONS; INFECTION; PROTEIN; EPITOPES;
D O I
10.1016/j.tube.2009.10.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The 6-kDa early secreted antigenic target (ESAT-6) is a T-cell antigen recognized by individuals infected with Mycobacterium tuberculosis. The aim of the study was to identify "protective epitopes'' of ESAT-6 protein in the south Indian population. Proliferative and Interferon gamma (IFN-gamma) responses to ESAT-6 peptides were studied by flow cytometry and Enzyme linked immunosorbent assay (ELISA). Healthy household contacts (HHC) recognized Esp1 (10/17) and Esp6 (9/17) peptides. Among pulmonary tuberculosis patients (PTB), Esp1 (3/11) and Esp6 (5/11) were recognized. Maximal response (7/10) was found for Esp1 and Esp8 in treated patients (TR). Median values for the responding subjects gave the following results: Esp1 (76 pg/ml), Esp6 (64 pg/ml), induced IFN-g production in HHC; PTB gave low IFN-g responses for the peptides. TR responded to the peptides Esp1 (141 pg/ml), Esp8 (102 pg/ml). The proliferation of CD4 cells was similar in both PTB and TR for all peptides; but HHC showed an increase for Esp1 (p < 0.05) and Esp6 (p < 0.01). Esp1 (amino acids aa 1-20) and Esp6 (aa 51-70) were the immunogenic peptides recognized by the alleles HLA DRB1*04 and HLA DRB1*10 among HHC. But the association of the alleles with ESAT-6 peptide presentation needs to be confirmed in a large cohort of subjects. We speculate that ESAT-6 can be used along with other immune-eliciting proteins for vaccine design strategies in south Indian population. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:60 / 69
页数:10
相关论文
共 50 条
  • [41] ESAT-6 undergoes self-association at phagosomal pH and an ESAT-6-specific nanobody restricts M. tuberculosis growth in macrophages
    Bates, Timothy A.
    Trank-Greene, Mila
    Nguyenla, Xammy
    Anastas, Aidan
    Gurmessa, Sintayehu K.
    Merutka, Ilaria R.
    Dixon, Shandee D.
    Shumate, Anthony
    Groncki, Abigail R.
    Parson, Matthew A. H.
    Ingram, Jessica R.
    Barklis, Eric
    Burke, John E.
    Shinde, Ujwal
    Ploegh, Hidde L.
    Tafesse, Fikadu G.
    [J]. ELIFE, 2024, 12
  • [42] Early diagnosis of tuberculous meningitis by an indirect ELISA protocol based on the detection of the antigen ESAT-6 in cerebrospinal fluid
    Song, F.
    Sun, X.
    Wang, X.
    Nai, Y.
    Liu, Z.
    [J]. IRISH JOURNAL OF MEDICAL SCIENCE, 2014, 183 (01) : 85 - 88
  • [43] Humoral Immune Responses against the Mycobacterium tuberculosis 38-Kilodalton, MTB48, and CFP-10/ESAT-6 Antigens in Tuberculosis
    Wu, Xueqiong
    Yang, Yourong
    Zhang, Junxian
    Li, Bangying
    Liang, Yan
    Zhang, Chuiying
    Dong, Mei
    Cheng, Hongbing
    He, Jufang
    [J]. CLINICAL AND VACCINE IMMUNOLOGY, 2010, 17 (03) : 372 - 375
  • [44] Factors associated with humoral response to ESAT-6, 38 kDa and 14 kDa in patients with a spectrum of tuberculosis
    Silva, VMC
    Kanaujia, G
    Gennaro, ML
    Menzies, D
    [J]. INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2003, 7 (05) : 478 - 484
  • [45] Uncommon presentations of tuberculosis:: the potential value of a novel diagnostic assay based on the Mycobacterium tuberculosis-specific antigens ESAT-6 and CFP-10
    Arend, SM
    Ottenhoff, THM
    Andersen, P
    van Dissel, JT
    [J]. INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2001, 5 (07) : 680 - 686
  • [46] ESAT-6 Inhibits Production of IFN-γ by Mycobacterium tuberculosis-Responsive Human T Cells
    Wang, Xisheng
    Barnes, Peter F.
    Dobos-Elder, Karen M.
    Townsend, James C.
    Chung, Yoon-tae
    Shams, Homayoun
    Weis, Stephen E.
    Samten, Buka
    [J]. JOURNAL OF IMMUNOLOGY, 2009, 182 (06) : 3668 - 3677
  • [47] A protein linkage map of the ESAT-6 secretion system 1 (ESX-1) of Mycobacterium tuberculosis
    Teutschbein, Janka
    Schumann, Gisbert
    Moellmann, Ute
    Grabley, Susanne
    Cole, Stewart T.
    Munder, Thomas
    [J]. MICROBIOLOGICAL RESEARCH, 2009, 164 (03) : 253 - 259
  • [48] Role of ESAT-6 in pathogenicity of Beijing and non-Beijing Mycobacterium tuberculosis isolates
    Mahghani, Ghorban Ali
    Kargar, Mohammad
    Ghaemi, Ezzat Allah
    Kafilzadeh, Farshid
    Davoodi, Homa
    [J]. MICROBIAL PATHOGENESIS, 2022, 162
  • [49] Cytotoxicity responses to selected ESAT-6 and CFP-10 peptides in tuberculosis
    Kumar, M. Madhan
    Raja, Alamelu
    [J]. CELLULAR IMMUNOLOGY, 2010, 265 (02) : 146 - 155
  • [50] An N-acetyltransferase required for ESAT-6 N-terminal acetylation and virulence in Mycobacterium marinum
    Collars, Owen A.
    Jones, Bradley S.
    Hu, Daniel D.
    Weaver, Simon D.
    Sherman, Taylor A.
    Champion, Matthew M.
    Champion, Patricia A.
    [J]. MBIO, 2023, 14 (05):