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  • Clinical and Experimental Health Sciences
  • Volume:2 Issue:6
  • Regulation of CD8+ Suppressor T cells with Pattern Recognition Receptors

Regulation of CD8+ Suppressor T cells with Pattern Recognition Receptors

Authors : Aysın TULUNAY, Hüseyin BİLGİN, Mehmet Onur ELBAŞI, Emel EKŞİOĞLU DEMİRALP
Pages : 0-0
View : 19 | Download : 8
Publication Date : 2014-01-30
Article Type : Research Paper
Abstract :Objective:  The suppressive effects of CD8+CD28- T cells on the proliferation of T helper cells have been demonstrated. Toll like receptors insert ignore into journalissuearticles values(TLRs);, the potent activators of innate immune response, are also expressed on T cells.  Methods:  We aimed to identify the phenotypic and functional characteristics of CD8+CD28- suppressive T cells insert ignore into journalissuearticles values(Ts); and how TLRs regulate their functions. Expressions of CD56, HLA-DR and perforin levels were analyzed. TLR expression kinetics of CD8+ cells were examined before and after stimulation with phytohemagglutinin insert ignore into journalissuearticles values(PHA);. Magnetically isolated Ts were stimulated with TLR agonists and their suppressive capacity was investigated using 5-ethynyl-2’-deoxyuridine insert ignore into journalissuearticles values(EDU);. Suppressive cytokines IL-10 and TGF-ß were analyzed with ELISA.  Results:  HLA-DR, CD56 and perforin expressions were found higher on Ts compared to Tef. Among Ts, two distinct populations, CD8+CD28-CD56+ and CD8+CD28-HLA-DR+, were identified. TLR expressions of Ts after PHA stimulation were found lower. We also demonstrated that these cells suppress the proliferation of CD4 T cells and secrete high levels of TGF-ß. TLR1/TLR2 and TLR3 agonists inhibited the suppressive function of Ts but TLR4 stimulation had no effect. Although we did not find any difference in the levels of TGF-ß secretion after TLR1/TLR2 stimulation, TGF-ß levels were reduced after TLR3 and TLR4 stimulations.  Conclusions:  We demonstrated that Ts suppress the CD4+ T cells via TGF-ß. However, this suppression can be inverted by TLR stimulation. When CD8+CD28- Ts encounter a strong stimulation like TLR3 stimulation, they lose their suppressive capacity and their plasticity enables them to differentiate into effector cells in order to sustain immune defense. Anahtar Kelimeler :  Regulatory T cells, TLR, suppression, pattern recognition receptors
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