以细菌dna为佐剂的多杀假单胞菌灭活疫苗免疫Balb/c小鼠后脾细胞和血清中细胞因子(IL-6和IL-12)的检测比较

Maryam Homayoon, Y. Tahamtan, M. Kargar
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引用次数: 4

摘要

目的:多杀性巴氏杆菌与鸟类和哺乳动物呼吸道的共生致病菌有关。本研究的目的是通过检测脾细胞和血清中细胞因子的变化,验证接种bDNAby佐剂铁灭活疫苗后Balb/c小鼠的细胞免疫应答。方法:用多杀假单胞菌灭活抗原免疫小鼠,观察免疫后各组小鼠脾细胞悬浮和血清细胞因子增殖情况。我们使用多杀假单胞菌A (AbDNA)、多杀假单胞菌B (BbDNA)、鼠伤寒沙门氏菌(SbDNA)细菌dna和明矾作为佐剂。ELISA法检测白细胞介素6 (IL-6)、IL-12滴度。结果:以bdna为佐剂的疫苗制剂免疫小鼠产生的白介素水平高于明矾组和对照组。免疫组动物血清中促炎因子(IL-6、IL-12)水平显著高于对照组(p<0.01)。IIA+SbDNA组体外刺激脾细胞中IL-6和IL-12的峰值分别为59.8 pg/ml和26.4 pg/ml。结论:这些发现表明,用细菌dna作为佐剂配制的多杀假单胞菌灭活抗原可能是抗多杀假单胞菌感染的候选疫苗。细菌dna对细胞免疫反应的影响可用于开发新疫苗。
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The Comparison Detection of Cytokines (IL-6 and IL-12) from Spleen Cells and Serums in Balb/c Mice after Immunization with Killed P. multocida Vaccines Co-formulated with Bacterial DNAs as Adjuvant
Purpose: Pasteurella multocida has been correlated with commensal pathogens in the respiratory tract of birds and mammals. The purpose of the present study was to verify the cellular immune responses in Balb/c mice inoculated with the iron inactivated vaccine adjuvanted with bDNAby the detection of cytokines from spleen cells and serum. Methods: Mice were experimentally immunized with P. multocida killed antigens to study the splenocyte suspension and serum cytokines proliferation at different groups of post-immunization. We used P. multocida A (AbDNA), P. multocida B (BbDNA), S. typhimurium (SbDNA) bacterial DNAs and alum as adjuvants. Interleukin-6 (IL-6) and IL-12 titer were tested by ELISA. Results: Mice immunized with vaccine formulations containing bDNAs as adjuvant produced a higher level of interleukins than alum and control groups. The serum level of pro-inflammatory cytokines (IL-6 and IL-12) was significantly higher (p<0.01) in vaccinated animals compared to control groups. A peak of IL-6 (59.8 pg/ml) and IL-12 (26.4 pg/ml) was recorded in in vitro stimulated splenocytes in the IIA+SbDNA group. Conclusion: These findings designated that killed P. multocida antigens formulated with bacterial DNAs as an adjuvant are possible vaccine candidates against P. multocida infections. The effect of the bacterial DNAs on the cellular immune response can be exploited in the development of new vaccines.
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