Published:2008
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高志云,揣侠,蓝佳明,王晓凌,张永红,王刚,王永祥.MDC、STxB与CVB3 VP1 融合DNA疫苗的免疫效果比较[J].陆军军医大学学报(原第三军医大学学报),2008,30(09):799-802.
GAO Zhi-yun CHUAI Xia,LAN Jia-ming,WANG Xiao-ling,ZHANG Yong-hong,WANG Gang,WANG Yong-xiang.Comparison on immune effects of MDC-VP1 and STxB-VP1 DNA vaccine in mice[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(09):799-802.
高志云,揣侠,蓝佳明,王晓凌,张永红,王刚,王永祥.MDC、STxB与CVB3 VP1 融合DNA疫苗的免疫效果比较[J].陆军军医大学学报(原第三军医大学学报),2008,30(09):799-802. DOI:
GAO Zhi-yun CHUAI Xia,LAN Jia-ming,WANG Xiao-ling,ZHANG Yong-hong,WANG Gang,WANG Yong-xiang.Comparison on immune effects of MDC-VP1 and STxB-VP1 DNA vaccine in mice[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(09):799-802. DOI:
目的 比较小鼠巨噬细胞源趋化因子(macrophage-derived chemokine
MDC)和志贺毒素B亚单位(Shiga toxin B subunit
STxB)与柯萨奇病毒B组3型(coxsackievirus B3
CVB3)VP1融合DNA疫苗的免疫效果。 方法 将120只雄性BALB/c小鼠分为6组,每组20只,分别肌内注射pcDNA3、pcDNA3/MDC、pcDNA3/STxB、pcDNA3/VP1、pcDNA3/MDC-VP1和pcDNA3/STxB-VP1,每3周1次,共3次,每次免疫后20 d取血清,用微量中和试验检测CVB3中和抗体,第3次免疫后3周,每组取3只小鼠,取脾脏制备脾细胞,用CCK-8法检测特异性CTL杀伤活性,其余小鼠用10LD
50
的CVB3攻击,观察小鼠的生存情况。 结果 pcDNA3/VP1、pcDNA3/STxB-VP1和pcDNA3/MDC-VP1组均能诱导小鼠产生中和抗体;除pcDNA3/STxB-VP1组外,另两组抗体滴度随免疫次数增加而提高;第3次免疫后,pcDNA3/MDC-VP1组平均抗体滴度和脾淋巴细胞特异性CTL杀伤活性高于pcDNA3/VP1(P0.05)。病毒攻击后
pcDNA3/MDC-VP1组21 d生存率高于其他各组(P0.05)。pcDNA3/STxB-VP1组抗体滴度和生存情况与pcDNA3/VP1组无明显差异。 结论 融合基因疫苗pcDNA3/MDC-VP1能诱导小鼠产生较强的体液和细胞免疫,提高了小鼠生存率,免疫效果优于pcDNA3/STxB-VP1。
Objective To compare the effect of macrophage-derived chemokine (MDC) and Shiga toxin B subunit (STxB) gene on the neutralizing antibodies and specific CTL response induced by Coxasckievirus B3 (CVB3) VP1 fusion DNA vaccine
as wells as the protective effect of the genes on the mice challenged with CVB3. Methods Male BALB/c mice were divided into 6 groups randomly
20 for each
an
d injected imtramuscularly (i.m.) pcDNA3
pcDNA3/MDC
pcDNA3/STxB
pcDNA3/VP1
pcDNA3/MDC-VP1
pcDNA3/STxB-VP1
once for 3 weeks
totally for 3 times. Serum samples 20 d after each injection were taken and detected for the neutralizing antibody against CVB3 by micro-neutralization test. Three weeks after the third immunization
splenocytes from 3 mice of each group were isolated to detect specific CTL response by CCK-8 assay. The mice were challenged with 10LD
50
of CVB3 after the 3 injections. The survival time and survival rate were observed. Results Neutralizing antibodies were induced in pcDNA3/VP1
pcDNA3/STxB-VP1 and pcDNA3/MDC-VP1 groups
and the antibody titers were increased with the increasing number of injections except pcDNA3/STxB-VP1 group. After the third inoculation
the mean neutralizing antibody titers in pcDNA3/MDC-VP1 group were higher than pcDNA3/VP1 and pcDNA3/STxB-VP1 groups (P0.05). Up to the 21st day after CVB3 challenge
the survival rates of pcDNA3/MDC-VP1 group were better than others (P0.05). However
neutralizing antibody and survival rate had no significant changes in pcDNA3/VP1 and pcDNA3/STxB-VP1 groups. Conclusion pcDNA3/MDC-VP1 vaccine can induce a stronger immunological effect
result in a higher survival rate
and had better influence than pcDNA3/STxB-VP1.
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