Noll A, Bücheler N, Bohn E, Schirmbeck R, Reimann J, Autenrieth I B
Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, LMU München, Germany.
Eur J Immunol. 1999 Mar;29(3):986-96. doi: 10.1002/(SICI)1521-4141(199903)29:03<986::AID-IMMU986>3.0.CO;2-9.
Naked plasmid DNA (pRc/Y-hsp60) with a cytomegalovirus promoter and a sequence encoding Yersinia enterocolitica 60-kDa heat shock protein (Y-HSP60) was used for vaccination. After intramuscular injection of pRc/Y-hsp60, Y-hsp60 mRNA could be detected by reverse transcription-PCR in muscle, liver and spleen. A single immunization with pRc/Y-hsp60 induced significant Y-HSP60-specific T cell responses after 1 week. IFN-gamma production by spleen cells upon stimulation with Y-HSP60 was strictly dependent on the presence of CD4+ T cells, indicating the generation of a Th1 response upon DNA immunization. DNA immunization in addition induced strong Y-HSP60-specific IgG2a, weak IgG1, but not IgA antibodies. Immunization of BALB/c and C57BL/6 mice with pRc/Y-hsp60 conferred protection against disseminated Y. enterocolitica infection in spleen, but not at the site of mucosal entry, the Peyer's patches. Furthermore, pRc/Y-hsp60 vaccination did not induce cross-protection against related pathogens. Vaccination of beta2-microglobulin- and H2-I-Abeta-deficient mice was not protective, suggesting that both CD4+ and CD8+ T cells are required for protective immunity induced by DNA vaccination.
携带巨细胞病毒启动子和编码小肠结肠炎耶尔森菌60 kDa热休克蛋白(Y-HSP60)序列的裸质粒DNA(pRc/Y-hsp60)被用于疫苗接种。肌肉注射pRc/Y-hsp60后,可通过逆转录PCR在肌肉、肝脏和脾脏中检测到Y-hsp60 mRNA。单次接种pRc/Y-hsp60在1周后诱导出显著的Y-HSP60特异性T细胞反应。用Y-HSP60刺激后,脾细胞产生的IFN-γ严格依赖于CD4+ T细胞的存在,表明DNA免疫诱导产生了Th1反应。DNA免疫还诱导产生了强Y-HSP60特异性IgG2a、弱IgG1,但未诱导产生IgA抗体。用pRc/Y-hsp60免疫BALB/c和C57BL/6小鼠可使其免受脾脏中播散性小肠结肠炎耶尔森菌感染的侵害,但在黏膜进入部位派伊尔结处则无此作用。此外,pRc/Y-hsp60疫苗接种未诱导对相关病原体的交叉保护。对β2-微球蛋白和H2-I-Aβ缺陷小鼠进行疫苗接种没有保护作用,这表明DNA疫苗诱导的保护性免疫需要CD4+和CD8+ T细胞。