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首页> 外文期刊>Clinical and vaccine immunology: CVI >A Leptospira borgpetersenii serovar Hardjo vaccine induces a Th1 response, activates NK cells, and reduces renal colonization.
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A Leptospira borgpetersenii serovar Hardjo vaccine induces a Th1 response, activates NK cells, and reduces renal colonization.

机译:一个钩端螺旋体borgpetersenii型Hardjo疫苗诱发Th1反应,激活NK细胞减少肾殖民。

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摘要

Chronic infection of cattle with Leptospira borgpetersenii serovar Hardjo reduces animal production through reproductive failure and presents a persistent health threat to workers in the animal industry. Cattle are maintenance hosts for serovar Hardjo, and development of vaccines that establish long-term protective immunity has been problematic; induction of high titers of anti-serovar Hardjo antibody does not appear to be protective. Rather, development of an antigen-specific Th1 response appears to be critical for limiting renal colonization and urinary shedding of bacteria. In this study we compared two monovalent killed bacterial cell vaccines to assess long-term (12 months) protection against live serovar Hardjo challenge. Although neither vaccine prevented infection, renal colonization and urinary shedding of bacteria were reduced compared to those of control animals. Increased proliferation of CD4(+), CD8(+), and gammadelta T cells from vaccinated, but not control, animals was detected. In addition, NK cells from vaccinated animals and from all animals following infection, when exposed to antigen ex vivo, demonstrated a gamma interferon (IFN-gamma) recall response. We propose that programming NK cells to respond quickly to L. borgpetersenii serovar Hardjo infection may be an important step toward developing protective immunity.
机译:慢性感染钩端螺旋体的牛borgpetersenii型Hardjo减少动物通过生殖失败和生产提出了一种持久的健康威胁工人动物产业。为型Hardjo,疫苗的发展建立长期保护性免疫是有问题的;anti-serovar Hardjo抗体没有出现被保护。抗原Th1反应似乎限制肾殖民和的关键尿脱落的细菌。两个单价相比细菌细胞死亡疫苗评估长期(12个月)抵御住型Hardjo挑战。尽管疫苗预防感染,肾的殖民和尿脱落细菌的减少相比控制动物。CD4 (+) T细胞CD8 (+), gammadelta接种疫苗,但不是控制、动物检测到。动物和动物感染后,当暴露于抗原体外,演示了一个γ干扰素(IFN-gamma)回忆起反应。建议编程NK细胞反应迅速l . borgpetersenii型Hardjo感染可能是重要的一步发展保护性免疫。

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