Beijing Institute of Biotechnology, Beijing, China.
Immunopharmacol Immunotoxicol. 2011 Mar;33(1):211-9. doi: 10.3109/08923971003782327.
Granulocyte-macrophage clony-stimulating factor (GM-CSF) is an attractive adjuvant for a DNA vaccine on account of its ability to recruit antigen-presenting cells to the site of antigen synthesis as well as stimulate the maturation of dendritic cells.This study evaluated the utility of GM-CSF as a plasmid DNA replicon vaccine adjuvants for botulinum neurotoxin serotype A (BoNT/A) in mouse model. In balb/c mice that received the plasmid DNA replicon vaccines derived from Semliki Forest virus (SFV) carrying the Hc gene of BoNT/A (AHc), both antibody and lymphoproliferative response specific to AHc were induced, the immunogenicity was enhanced by co-delivery or coexpress of the GM-CSF gene. In particular, when AHc and GM-CSF were coexpressed within the SFV based DNA vaccine, the anti-AHc antibody titers and survival rates of immunized mice after challenged with BoNT/A were significantly increased, and further enhanced by coimmunization with aluminum phosphate adjuvant.
粒细胞-巨噬细胞集落刺激因子 (GM-CSF) 是一种有吸引力的 DNA 疫苗佐剂,因为它能够将抗原呈递细胞募集到抗原合成部位,并刺激树突状细胞的成熟。本研究评估了 GM-CSF 作为质粒 DNA 复制子疫苗佐剂在小鼠模型中对肉毒毒素血清型 A (BoNT/A) 的应用。在接受携带 BoNT/A Hc 基因的 Semliki Forest 病毒 (SFV) 质粒 DNA 复制子疫苗 (AHc) 的 balb/c 小鼠中,均诱导出针对 AHc 的抗体和淋巴细胞增殖反应,GM-CSF 基因的共递送或共表达增强了免疫原性。特别是,当 AHc 和 GM-CSF 在基于 SFV 的 DNA 疫苗中共表达时,免疫小鼠在受到 BoNT/A 攻击后的抗-AHc 抗体滴度和存活率显著提高,并且通过与铝磷酸佐剂共同免疫进一步增强。