Zhang Ailian, Yang Yu, Wang Yan, Zhao Gan, Yang Xiumei, Wang Danyang, Wang Bin
College of Life Science and Technology, Xinjiang University, 14 Shengli Road, Urumqi 830046, Xinjiang, China.
College of Life Science and Technology, Xinjiang University, 14 Shengli Road, Urumqi 830046, Xinjiang, China.
Vaccine. 2017 Feb 15;35(7):1037-1045. doi: 10.1016/j.vaccine.2017.01.002. Epub 2017 Jan 19.
Activating innate immunity by an adjuvant is required in vaccine development. The study aims to investigate adjuvant effects of aqueous extracts of Artemisia rupestris L. (AEAR) in vivo and in vitro. ICR mice were subcutaneously administered with antigen and AEAR at various doses to evaluate their immune responses of antibodies, dendritic cells (DCs), regulatory T cells (Treg), splenic lymphocyte, and cytokine. The evaluation results showed that AEAR could largely increase titers of antigen-specific antibodies (IgG, IgG, and IgG) and T cell proliferation. AEAR also increased expression of IFN-γ in CD8T cells as well as IL-4 and INF-γ expression in CD4T cells. Expression levels of MHC-II, CD40, CD80, and CD86 on DCs were significantly elevated, whereas the Treg frequency was significantly decreased. AEAR (200μg) showed remarkable adjuvant activity. Furthermore, AEAR enhanced MHC-II, CD40, CD80, and CD86 expression as well as the yields of TNF-α and IL-12 on DCs through toll-like receptor4 (TLR4) in vitro. Those results indicated that AEAR could serve as an efficacious immune stimulator for vaccines because it significantly enhanced specific immune responses by promoting DCs maturation and reduced Treg through TLR4 signaling pathway.
疫苗研发中需要佐剂激活先天免疫。本研究旨在探讨岩蒿水提取物(AEAR)在体内和体外的佐剂效应。将不同剂量的抗原和AEAR皮下注射给ICR小鼠,以评估其抗体、树突状细胞(DC)、调节性T细胞(Treg)、脾淋巴细胞和细胞因子的免疫反应。评估结果表明,AEAR可大幅提高抗原特异性抗体(IgG1、IgG2a和IgG2b)的滴度以及T细胞增殖。AEAR还增加了CD8+T细胞中IFN-γ的表达以及CD4+T细胞中IL-4和INF-γ的表达。DC上MHC-II、CD40、CD80和CD86的表达水平显著升高,而Treg频率显著降低。AEAR(200μg)表现出显著的佐剂活性。此外,体外实验中AEAR通过Toll样受体4(TLR4)增强了DC上MHC-II、CD40、CD80和CD86的表达以及TNF-α和IL-12的产生。这些结果表明,AEAR可作为疫苗的有效免疫刺激剂,因为它通过促进DC成熟显著增强特异性免疫反应,并通过TLR4信号通路减少Treg。