Chen Austen Y, Fry Scott R, Daggard Grant E, Mukkur Trilochan K S
Department of Biological and Physical Sciences, University of Southern Queensland, Toowoomba, Queensland, Australia.
Vaccine. 2008 Aug 12;26(34):4372-8. doi: 10.1016/j.vaccine.2008.06.005. Epub 2008 Jun 20.
Intramuscular immunization of mice with DNA cocktail vaccines, comprising potential protective antigens P36, P46, NrdF, and P97or P97R1 of Mycoplasma hyopneumoniae, induced strong Th1-polarized immune responses against each antigen, with only P46 eliciting a serum IgG response. Subcutaneous immunization with protein cocktail vaccines, surprisingly, induced both Th1-polarized immune response as well as antibody response whereas mice immunized with DNA cocktail vaccines followed by boosting with protein cocktail vaccines generated strong Th1-polarized and humoral immune responses. P97 was not recognized by serum antibodies from commercial bacterin-immunized mice indicating potential lack of expression of this important antigen in inactivated whole-cell vaccines.
用包含猪肺炎支原体潜在保护性抗原P36、P46、NrdF和P97或P97R1的DNA混合疫苗对小鼠进行肌肉注射免疫,可诱导针对每种抗原的强烈Th1极化免疫反应,只有P46能引发血清IgG反应。令人惊讶的是,用蛋白质混合疫苗进行皮下免疫可诱导Th1极化免疫反应以及抗体反应,而先用DNA混合疫苗免疫小鼠,随后用蛋白质混合疫苗加强免疫,则会产生强烈的Th1极化和体液免疫反应。商业灭活疫苗免疫小鼠的血清抗体无法识别P97,这表明这种重要抗原在灭活全细胞疫苗中可能缺乏表达。