Song Nan-nan, Wang Bing-xiang, Shi Da-zhong, Fu Lin-feng, Luo Yu, Yu Hong-juan, Han Shao-bo, Jiao Lei, Qie Ya-qing, Wang Hong-hai, Zhang Ying, Zhu Bing-dong
Lanzhou Center for Tuberculosis Research, Institute of Pathogenic Biology, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.
Zhonghua Jie He He Hu Xi Za Zhi. 2009 Jul;32(7):513-6.
To investigate the activity of a novel adjuvant consisting of dimethyldioctyldecyl ammonium bromide (DDA) and BCG polysaccharide nucleic acid (BCG-PSN).
BCG-PSN was extracted by hot-phenol method, and combined with DDA and Mycobacterium tuberculosis fusion antigen AMM (Ag85B-MPT64(190-198)-Mtb8.4) to formulate the Mycobacterium tuberculosis subunit vaccine. Mice were immunized subcutaneously with a 2-week interval between the immunizations (0.2 ml/dose), and humoral and cell-mediated immunity were detected by ELISA and ELISPOT respectively.
With the stimulation of Ag85B in vitro, the number of antigen specific IFN-gamma producing spleen lymphocytes were 222 +/- 79, 259 +/- 85, 230 +/- 64 per million respectively in the mice immunized with AMM + DDA + BCG-PSN, AMM + DDA, and BCG. Spleen lymphocytes in these 3 groups produced higher levels of IFN-gamma compared to the groups with the adjuvant of IFA or BCG-PSN alone or without adjuvant upon stimulation with Ag85B (t = 2.923-7.118, P < 0.05). Furthermore, the adjuvant consisting of DDA and BCG-PSN increased the ratio of Ig(2a)/IgG1 than DDA alone (0.125 vs. 0.025). Combined with AMM, the adjuvant DDA and the one consisting of DDA and BCG-PSN induced higher level of immunity than incomplete Freund's adjuvant (IFA), NaCl, and BCG-PSN alone.
Mycobacterium tuberculosis subunit vaccine AMM + DDA + BCG-PSN induced a strong Th1-type immune response, and DDA + BCG-PSN, especially DDA promoted the immune response of the M. tuberculosis subunit vaccine in mice.
研究由二甲基二辛基癸基溴化铵(DDA)和卡介苗多糖核酸(BCG - PSN)组成的新型佐剂的活性。
采用热酚法提取BCG - PSN,并与DDA及结核分枝杆菌融合抗原AMM(Ag85B - MPT64(190 - 198) - Mtb8.4)联合制备结核分枝杆菌亚单位疫苗。小鼠皮下免疫,免疫间隔为2周(0.2 ml/剂量),分别通过ELISA和ELISPOT检测体液免疫和细胞介导免疫。
在体外Ag85B刺激下,用AMM + DDA + BCG - PSN、AMM + DDA和BCG免疫的小鼠中,每百万个脾淋巴细胞中产生抗原特异性IFN -γ的细胞数分别为222±79、259±85、230±64。在用Ag85B刺激后,这3组脾淋巴细胞产生的IFN -γ水平高于单独使用IFA或BCG - PSN佐剂组或无佐剂组(t = 2.923 - 7.118,P < 0.05)。此外,由DDA和BCG - PSN组成的佐剂比单独的DDA增加了Ig(2a)/IgG1的比例(0.125对0.025)。与AMM联合使用时,佐剂DDA以及由DDA和BCG - PSN组成的佐剂诱导的免疫水平高于不完全弗氏佐剂(IFA)、NaCl和单独的BCG - PSN。
结核分枝杆菌亚单位疫苗AMM + DDA + BCG - PSN诱导了强烈的Th1型免疫反应,DDA + BCG - PSN,尤其是DDA促进了结核分枝杆菌亚单位疫苗在小鼠中的免疫反应。