| Literature DB >> 24170093 |
Guohua Feng1, Ji-Yuan Zhang, Qing-Lei Zeng, Lei Jin, Junliang Fu, Bin Yang, Ying Sun, Tianjun Jiang, Xiangsheng Xu, Zheng Zhang, Jinhong Yuan, Liyuan Wu, Fu-Sheng Wang.
Abstract
Interleukin-21 (IL-21)+CD4+ T cells are involved in the immune response against hepatitis B virus (HBV) by secreting IL-21. However, the role of IL-21+CD4+ T cells in the immune response against chronic hepatitis C (CHC) virus infection is poorly understood. This study aimed to investigate the role of IL-21+CD4+ T cells in CHC patients and the potential mechanisms. The study subjects included nineteen CHC patients who were grouped by viral load (low, < 10(6) RNA copies/ml, n = 8; high, > 10(6) RNA copies/ml, n = 11). The peripheral frequency of HCV-specific IL-21+CD4+ T cells was higher in the low viral load group and was negatively correlated with the serum HCV RNA viral load in all CHC patients. Meanwhile, IL-21+ cells accumulated in the liver in the low viral load group. In vitro, IL-21 treatment increased the expression of proliferation markers and cytolytic molecules on HCV-specific CD8+ T cells. In summary, these findings suggest that HCV-specific IL-21+CD4+ T cells might contribute to HCV control by rescuing HCV-specific CD8+ T cells in CHC patients.Entities:
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Year: 2013 PMID: 24170093 PMCID: PMC3887990 DOI: 10.1007/s10059-013-0181-z
Source DB: PubMed Journal: Mol Cells ISSN: 1016-8478 Impact factor: 5.034