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[二甲基二十八烷基溴化铵-卡介苗多糖核酸佐剂增强结核分枝杆菌亚单位疫苗的免疫原性]

[Dimo-thylidioctyl ammonium bromide-BCG polysaccharide nucleic acid adjuvant enhanced the immunogenicity of a Mycobacterium tuberculosis subunit vaccine].

作者信息

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

机构信息

Lanzhou Center for Tuberculosis Research, Institute of Pathogenic Biology, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2009 Jul;32(7):513-6.

Abstract

OBJECTIVE

To investigate the activity of a novel adjuvant consisting of dimethyldioctyldecyl ammonium bromide (DDA) and BCG polysaccharide nucleic acid (BCG-PSN).

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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