Salam Mohammad Abdus, Katz Jannet, Zhang Ping, Hajishengallis George, Michalek Suzanne M
Department of Microbiology, University of Alabama at Birmingham, 845 19th Street South, BBRB 258/5, 35294-2170, USA.
Vaccine. 2006 Jun 5;24(23):5003-15. doi: 10.1016/j.vaccine.2006.03.044. Epub 2006 Mar 31.
The purpose of the present study was to determine if a Salmonella vector expressing the cloned saliva-binding region (SBR) of Streptococcus mutans or SBR linked to the A2 and B subunits of cholera toxin (CTA2/B) under the control of both the T7 and nirB promoters (T7-nirB dual promoter) was more effective in inducing mucosal and systemic anti-SBR antibody responses than Salmonella clones expressing the same antigens but under the control of either the nirB or T7 promoter. Mice were immunized by the intranasal route on days 0, 18 and 320 with Salmonella enterica serovar Typhimurium strain BRD 509 containing one of six plasmids encoding SBR or SBR-CTA2/B under the control of the T7-nirB, T7, or nirB promoter. Serum, saliva and vaginal wash samples were collected throughout the experiment and assessed for antibody activity by ELISA. Evidence is provided that Salmonella clones expressing SBR or SBR-CAT2/B under the control of either the T7 or T7-nirB promoter induced a high and persistent mucosal and systemic anti-SBR antibody response. All Salmonella clones induced good anti-SBR responses following the boost on day 320.
本研究的目的是确定在T7和nirB启动子(T7-nirB双启动子)控制下,表达变形链球菌克隆唾液结合区(SBR)或与霍乱毒素A2和B亚基(CTA2/B)相连的SBR的沙门氏菌载体,与表达相同抗原但受nirB或T7启动子控制的沙门氏菌克隆相比,在诱导粘膜和全身抗SBR抗体反应方面是否更有效。在第0、18和320天,用含有六种编码SBR或SBR-CTA2/B质粒之一的鼠伤寒沙门氏菌肠炎血清型鼠伤寒菌株BRD 509,通过鼻内途径对小鼠进行免疫,这些质粒在T7-nirB、T7或nirB启动子控制下。在整个实验过程中收集血清、唾液和阴道冲洗液样本,并通过ELISA评估抗体活性。有证据表明,在T7或T7-nirB启动子控制下表达SBR或SBR-CAT2/B的沙门氏菌克隆诱导了高且持续的粘膜和全身抗SBR抗体反应。在第320天加强免疫后,所有沙门氏菌克隆均诱导了良好的抗SBR反应。