Xie Xiaoping, Geng Shuang, Liu Hu, Li Chaofan, Yang Yuqin, Wang Bin
State Key Laboratory for Agro-Biotechnology; College of Biological Science; China Agricultural University; Beijing, PR China.
Key Laboratory of Medical Molecular Virology of MOH and MOE; Fudan University Shanghai Medical College; Shanghai, PR China.
Hum Vaccin Immunother. 2014;10(6):1688-99. doi: 10.4161/hv.28517. Epub 2014 Mar 18.
Previously, we have reported that either CIM or PZQ, 2 clinical drugs, could be used to develop as adjuvants on HBV DNA vaccine to elicit both humoral and cellular immune responses. Here, we demonstrate that combinations of CIM and PZQ as adjuvants for a HBV DNA vaccine, could induce much stronger antigen specific CD4(+) and CD8(+) T cell responses compared either with CIM or PZQ alone. The synergistic effects of CIM plus PZQ to HBV DNA vaccine were observed on a higher IgG2a/IgG1 ratio, an increase of HBsAg-specific CD4(+) T cells capable of producing IFN-γ or IL-17A and a robust IFN-γ-, IL-17A-, or TNF-α-producing CD8(+) T cells to HBsAg. Most importantly, the antigen-specific CTL response was also elevated significantly, which is critical for the eradication of hepatitis B virus (HBV) infected cells. Using an HBsAg transgenic mouse model, the expression of HBsAg in the hepatic cells was also significantly reduced after immunized with pCD-S 2 in the presence of 0.5% CIM and 0.25% PZQ. Further investigations demonstrated that the synergistic effects of combination of CIM and PZQ were dependent on enhanced cytotoxic CD8(+) T cells, which was correlated with impaired activities of regulatory T cells. Therefore, combinations of CIM and PZQ have great potential to be used as effective adjuvants on DNA-based vaccinations for the treatment of chronic hepatitis B.
此前,我们曾报道过,两种临床药物CIM或PZQ都可开发用作乙肝病毒(HBV)DNA疫苗的佐剂,以引发体液免疫和细胞免疫反应。在此,我们证明,CIM和PZQ联合用作HBV DNA疫苗的佐剂,与单独使用CIM或PZQ相比,可诱导更强的抗原特异性CD4(+)和CD8(+) T细胞反应。观察到CIM加PZQ对HBV DNA疫苗的协同作用体现在更高的IgG2a/IgG1比值、能够产生IFN-γ或IL-17A的HBsAg特异性CD4(+) T细胞增加以及对HBsAg产生强大的IFN-γ、IL-17A或TNF-α的CD8(+) T细胞。最重要的是,抗原特异性CTL反应也显著升高,这对于清除乙肝病毒(HBV)感染细胞至关重要。使用HBsAg转基因小鼠模型,在存在0.5% CIM和0.25% PZQ的情况下用pCD-S 2免疫后,肝细胞中HBsAg的表达也显著降低。进一步研究表明,CIM和PZQ联合的协同作用依赖于细胞毒性CD8(+) T细胞的增强,这与调节性T细胞活性受损相关。因此,CIM和PZQ联合用作基于DNA的疫苗接种治疗慢性乙型肝炎的有效佐剂具有巨大潜力。