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杨晓红, 吴静, 殷国荣, 刘娟娟, 孟晓丽, 申金雁. ESA和STAg鼻内免疫小鼠抗弓形虫感染作用[J]. 中国公共卫生, 2009, 25(3): 292-294. DOI: 10.11847/zgggws2009-25-03-21
引用本文: 杨晓红, 吴静, 殷国荣, 刘娟娟, 孟晓丽, 申金雁. ESA和STAg鼻内免疫小鼠抗弓形虫感染作用[J]. 中国公共卫生, 2009, 25(3): 292-294. DOI: 10.11847/zgggws2009-25-03-21
YANG Xiao-hong, WU Jing, YIN Guo-rong, . Intranasal immunization with ESA and STAg protects mice against Toxoplasma gondii infection[J]. Chinese Journal of Public Health, 2009, 25(3): 292-294. DOI: 10.11847/zgggws2009-25-03-21
Citation: YANG Xiao-hong, WU Jing, YIN Guo-rong, . Intranasal immunization with ESA and STAg protects mice against Toxoplasma gondii infection[J]. Chinese Journal of Public Health, 2009, 25(3): 292-294. DOI: 10.11847/zgggws2009-25-03-21

ESA和STAg鼻内免疫小鼠抗弓形虫感染作用

Intranasal immunization with ESA and STAg protects mice against Toxoplasma gondii infection

  • 摘要: 目的 观察弓形虫速殖子排泄一分泌抗原(excreted/secreted antigen,ESA)和可溶性速殖子抗原(solubletachyzoite antigen,STAg)鼻内免疫小鼠诱导的抗弓形虫感染作用。方法 BALB/c小鼠64只随机分为4组,每组16只,分别用磷酸盐缓冲液(PBS)(对照组)20μl/只、体外排泄-分泌抗原(excreted/secreted antigen in vitro,ESAv)20μg/只、腹腔排泄-分泌抗原(excreted/secreted antigen in mice,ESAm)20μg/只和STAg20μg/只滴鼻免疫小鼠2次,间隔14 d。末次免疫后14 d每组处死8只小鼠,ELISA法检测血清IgG和小肠冲洗液sIgA。每组剩余8只小鼠用RH株弓形虫速殖子1×104个/只灌胃攻击,记录小鼠健康情况。攻击后30 d处死小鼠,计数脾、脑组织内弓形虫虫荷(速殖子数)。结果 ESAm组小鼠于2次免疫后出现轻微竖毛、倦怠等症状,其他各组小鼠健康状况良好。免疫后14 d,各抗原组血清IgG水平均明显高于对照组(P<0.001);ESAv(P<0.05)、ESAm(P<0.001)和STAg(P<0.001)组肠液sIgA水平明显高于对照组,EsAm(P<0.001)和sTAg(P<0.05)组高于EsAv组。弓形虫攻虫后:30 d,各抗原组小鼠脾、脑组织内虫荷显著低于对照组(P<0.01),ESAv、ESAm和sTAg组脾内速殖子减虫率分别为49.2%,49.52%和51.94%,脑内减虫率分别为46.83%,50.81%和51.18%。结论 ESAv、ESAm和STAg鼻内免疫均能产生抗弓形虫感染的部分保护,但ESAm可能对机体有毒副作用,不适宜直接鼻内免疫。

     

    Abstract: Objective To study the protective immunity against Toxoplasma gondii induced by intranasal immunization with excreted/secreted antigens(ESA)and soluble tachyzoite antigen(STAg)in mice.Methods Sixty-four BALB/c mice were randomly divided into four groups.The control group was in tranasally treated with 20μl PBS permouse and the test groups treated with 20μg ESA in vitro(ESAv),ESA from peritoneal fluids(ESAm)or STAg permouse,respectively,twice at an internal of 2 weeks.Eightmice of each group were killed on day 14 th after the last immunization.Serum IgG and slgA in intestinal washes were detected by ELISA.Eightmice were challenged intragastrically with 1×104 tachyzoites permouse on day 14 th after the last immunization.Mice were killed on the 30 th day after the challenge,the tachyzoites in their spleens and brains were counted.Results Mice in ESA from peritoneal fluids group appeared slight piloerection and lassitude,while mice in other groups were healthy.The level of serum IgG in all antigen groups was higher than that of PBS group on 14 day after immunization(P<0.001).The levels of slgA in ESAv group(P<0.05),ESAm group(P<0.001) and STAg group(P<0.001)was higher than that of PBS group,and the levels in ESAm group(P<0.001)and STAg group(P<0.05)were higher than that of ESAv group.The tachyzoite load in spleens and brains in all antigen groups was significantly lower than that of PBS group(P<0.05).Compared with PBS group,The tachyzoite load in spleens of ESAv group,ESAm group and STAg groupd decreased with a percentages of 49.2%,49.52% and 51.94% in the spleens,respectively,and 46.83%,50.81% and 51.18% in the brains,respectively.Conclusion Intranasal immunization with ESA in vitro,ESA from peritoneal fluids or STAg can effectively induce immune responses against Toxoplasma gondii.ESA from peritoneal fluids has toxic side effect on mice.ESA in vitro and STAg may be attractive candidate for Toxop lasma gondii vaccine.

     

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