Evaluation of Interleukin17and Interleukin 23 expression in patients with active and latent tuberculosis infection

نویسندگان

  • Aghigh Ziaeemehr Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Amir Asnaashari Chronic Obstructive Pulmonary Disease Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Fatemeh Heidarnezhad Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Houshang Rafatpanah Rheumatic Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Kiarash Ghazvini Antimicrobial Resistance Research Canter, Mashhad University of Medical Sciences, Mashhad, Iran
  • Narges Valizadeh Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Reza Basiri Chronic Obstructive Pulmonary Disease Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Roghayeh Ghezelsofla Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Seyed Abdolrahim Rezaee Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Somayeh Sobhani Inflammation and Inflammatory Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
چکیده مقاله:

Objective(s): Tuberculosis is one of the most important infectious diseases with high mortality rates worldwide, especially in developing countries. Interleukin17 (IL-17) is an important acquired immunity cytokine, which is mainly produced by CD4+TH17 cells. It can recruit neutrophils and macrophages to the infected site in the lungs. IL-23 is one of the most important inducers of IL-17. In the present study, the expressions of IL-23 and IL-17 were examined in the pathogenesis of tuberculosis. Materials and Methods: Peripheral blood mononuclear cells (PBMCs) were isolated from subjects with latent tuberculosis infection (LTB) and newly diagnosed active tuberculosis patients (ATB). PBMCs were activated with purified protein derivative (PPD) for 72 hr. Activated cells were harvested, RNA was extracted, and cDNA was synthesized. IL-17 and IL-23 mRNA expressions were evaluated by real-time PCR. The frequency of Th17 cells was examined by flowcytometry. Results: The expressions of IL-17 and IL-23 mRNA were lower in patients than subjects with LTB (P

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evaluation of interleukin17and interleukin 23 expression in patients with active and latent tuberculosis infection

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عنوان ژورنال

دوره 19  شماره 8

صفحات  844- 850

تاریخ انتشار 2016-08-01

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