مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

310
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

173
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

EXPRESSION AND PURIFICATION OF RECOMBINANT MYCOBACTERIUM TUBERCULOSIS DIAGNOSIS ANTIGENS, ESAT-6, CFP-10, AND ESAT-6/CFP-10, AND THEIR POTENTIAL USE IN THE DIAGNOSIS AND DETECTION OF TUBERCULOSIS

Pages

  558-565

Abstract

 Background: One of the most widely used methods to detect tuberculosis (TB) infection is the tuberculin skin test (TST).full Sequencing of the MYCOBACTERIUM TUBERCULOSIS (M.tb) genome has led to the identification of several antigens that can be utilized for accurate diagnosis and control of TB. The aim of this study is to produce and purify several specific recombinant M.tb antigens in order to evaluate their potential use in the diagnosis of TB.Materials and Methods: The recombinant secretory antigens ESAT-6, CFP-10, and ESAT-6/CFP-10 were produced through PCR and cloning methods. To investigate the antigen-specific responses of these recombinant antigens in the detection of TB, ex vivo enzyme-linked immunospot (ELISPOT) tests were performed on samples of 30 clinically diagnosed TB patients.Results: Throughout this study, the selected M.tb antigens were cloned, expressed, and purified in Escherichia coli (BL21).The ELISPOT assays for the detection of TB showed sensitivity values of 93%, 90%, and 100% for recombinant ESAT-6, CFP-10, and ESAT-6/CFP-10 proteins, respectively, which were significantly higher than the values obtained in conventional tuberculin skin test (TST).Conclusions: Our results show that these recombinant antigens can be used as an accurate detecting TB test for Iranian Patients.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    HEMMATI, M., SEGHATOLESLAM, A., RASTI, M., EBADAT, S., MOSAVARI, N., HABIBAGAHI, M., TAHERI, M., SARDARIAN, A., & MOSTAFAVIPOUR, Z.. (2011). EXPRESSION AND PURIFICATION OF RECOMBINANT MYCOBACTERIUM TUBERCULOSIS DIAGNOSIS ANTIGENS, ESAT-6, CFP-10, AND ESAT-6/CFP-10, AND THEIR POTENTIAL USE IN THE DIAGNOSIS AND DETECTION OF TUBERCULOSIS. IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), 13(8), 558-565. SID. https://sid.ir/paper/292386/en

    Vancouver: Copy

    HEMMATI M., SEGHATOLESLAM A., RASTI M., EBADAT S., MOSAVARI N., HABIBAGAHI M., TAHERI M., SARDARIAN A., MOSTAFAVIPOUR Z.. EXPRESSION AND PURIFICATION OF RECOMBINANT MYCOBACTERIUM TUBERCULOSIS DIAGNOSIS ANTIGENS, ESAT-6, CFP-10, AND ESAT-6/CFP-10, AND THEIR POTENTIAL USE IN THE DIAGNOSIS AND DETECTION OF TUBERCULOSIS. IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ)[Internet]. 2011;13(8):558-565. Available from: https://sid.ir/paper/292386/en

    IEEE: Copy

    M. HEMMATI, A. SEGHATOLESLAM, M. RASTI, S. EBADAT, N. MOSAVARI, M. HABIBAGAHI, M. TAHERI, A. SARDARIAN, and Z. MOSTAFAVIPOUR, “EXPRESSION AND PURIFICATION OF RECOMBINANT MYCOBACTERIUM TUBERCULOSIS DIAGNOSIS ANTIGENS, ESAT-6, CFP-10, AND ESAT-6/CFP-10, AND THEIR POTENTIAL USE IN THE DIAGNOSIS AND DETECTION OF TUBERCULOSIS,” IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), vol. 13, no. 8, pp. 558–565, 2011, [Online]. Available: https://sid.ir/paper/292386/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button