Identification of IL-10-secreting CD8+CD28−PD-1+ regulatory T cells associated with chronic hepatitis C virus infection

•CD8+CD28−PD-1+ Tregs correlate with the infection of HCV.•CD8+CD28−PD-1+ Tregs secret IL-10 inhibit the proliferation of CTL.•CD8+CD28−PD-1+ Tregs induce the apoptosis of CTL. CD8+CD28− regulatory T cells (Tregs) play important roles in chronic viral infections. Programmed death 1 (PD-1) is highly...

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Veröffentlicht in:Immunology letters 2018-10, Vol.202, p.16-22
Hauptverfasser: Wang, Weihong, Tong, Zhaowei, Zhong, Jianfeng, Zhang, Longqi, Zhang, Hui, Su, Yanguang, Gao, Bingbing, Zhang, Chun
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Sprache:eng
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Zusammenfassung:•CD8+CD28−PD-1+ Tregs correlate with the infection of HCV.•CD8+CD28−PD-1+ Tregs secret IL-10 inhibit the proliferation of CTL.•CD8+CD28−PD-1+ Tregs induce the apoptosis of CTL. CD8+CD28− regulatory T cells (Tregs) play important roles in chronic viral infections. Programmed death 1 (PD-1) is highly expressed on hepatitis C virus (HCV)-specific CTLs. However, little is known regarding the role of CD8+CD28-PD1+ T cells in hepatitis C. Herein, we found that the frequency of CD8+CD28−PD1+, but not CD8+CD28−PD1− T cells, correlated with markers of chronic hepatitis C virus (HCV) infection and the response to treatment. Our results showed that CD8+CD28-PD1+ T cells were significantly elevated in chronic HCV-infected patients and there was a distinct correlation between the frequency of CD8+CD28-PD1+ T cells and serum levels of HCV RNA. During a 48-week course of treatment with peg-IFN-a2a plus ribavirin, dynamic changes in the frequencies of CD8+CD28-PD1+ T cells were observed, associated with the virologic response. IL-10 secretion may explain the suppressive function of CD8+CD28-PD1+ T cells in chronic HCV-infected patients. Overall, our study demonstrates that PD-1 is an important marker of CD8+CD28− Tregs in chronic HCV infection. Thus, the frequency and regulatory function of CD8+CD28-PD1+ T cells play vital roles in HCV infection and the response to treatment.
ISSN:0165-2478
1879-0542
DOI:10.1016/j.imlet.2018.07.008