Author/Authors :
Mohammadi Nejad, Mozafar Razi Herbal Medicine Research Center - Lorestan University of Medical Sciences, Khorramabad , Salehi, Eisa Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Mesdaghi, Mehrnaz Department of Immunology - Mofid Children Hospital - Shahid Beheshti University of Medical Sciences, Tehran , Atarod, Lida Vali-Asr Hospital - Tehran University of Medical Sciences, Tehran , Movahedi, Masoud Children Medical Center - Tehran University of Medical Sciences, Tehran , Gheflati, Zahra Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Aboufazeli, Tahereh Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran , Vodjgani, Mohammad Department of Immunology - School of Medicine - Tehran University of Medical Sciences, Tehran
Abstract :
Allergic rhinitis (AR) is an inflammatory disorder of the nasal mucosa with high
morbidity and prevalence. Natural killer (NK) cells might have a role in AR. We aimed to
evaluate the changes of the markers and receptors on NK cells in AR patients compared to
the non-atopic controls.
Flow cytometric analysis was used with double staining of the Peripheral Blood
Mononuclear Cells (PBMCs) to examine the expression of CD25 and CD69 markers, and
NKG2D and NKG2A receptors on NK cells of 20 patients with AR and 20 non-atopic
controls. The serum total IgE level was measured by Enzyme-linked Immunosorbent Assay.
The expression of CD69 antigen on NK cells in AR patients was significantly higher than
that of healthy group (p=0.03). No significant changes were observed between CD25,
NKG2D and NKG2A expression on the surface of NK cells from healthy and AR subjects.
Our study also showed that there was no significant correlation between the expression of
CD69, CD25, NKG2D and NKG2A and level of serum total IgE in AR patients and normal
subjects.
These results indicated that the expression of CD69 antigen on NK cells of AR patients
was increased. The high expression of CD69 on NK cells in AR patients suggested that these
cells were activated, probably due to the cytokines secreted from allergen-stimulated T cells
and activated monocytes.