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初次接种 LiESP/QA-21 疫苗(CaniLeish®)后,犬体内产生的保护性免疫应答在一年后仍能有效抵抗实验性挑战。

The protective immune response produced in dogs after primary vaccination with the LiESP/QA-21 vaccine (CaniLeish®) remains effective against an experimental challenge one year later.

机构信息

Medical Department, Virbac, Carros, France.

出版信息

Vet Res. 2014 Jun 25;45(1):69. doi: 10.1186/1297-9716-45-69.

Abstract

Control of canine leishmaniasis is an important objective for the benefit of dogs living in or visiting endemic areas and for public health because of the zoonotic nature of this disease. Resistance or susceptibility to developing canine leishmaniasis after exposure to Leishmania infantum is primarily determined by the ability of the immune system to develop an appropriate Th1-dominated specific response to the parasite. For this reason there is a need for effective canine vaccines that can decrease the number of dogs developing progressive infections. In this study, we followed the impact of the LiESP/QA-21 canine vaccine (composed of excreted-secreted proteins of L. infantum and the QA-21 saponin adjuvant), recently launched commercially in Europe, on selected humoral and cellular immune parameters following an infectious intravenous challenge with L. infantum promastigotes administered one year after the primary vaccine course. We also followed parasitological parameters to determine the parasitological status of the challenged dogs. In contrast to controls, vaccinated dogs retained significantly stronger cell-mediated immune responses against the parasite despite a virulent challenge and had significantly lower mean parasite burdens at the end of the study, associated with a lower probability of developing active infections. These results confirm that the immune responses generated by vaccination with LiESP/QA-21 are still effective against an intravenous challenge one year after the primary vaccine course.

摘要

控制犬利什曼病对于生活在或访问流行地区的犬以及公共卫生来说是一个重要目标,因为这种疾病具有人畜共患的性质。在接触利什曼原虫后,对犬利什曼病产生抗性或易感性主要取决于免疫系统产生针对寄生虫的适当 Th1 优势特异性反应的能力。出于这个原因,需要有效的犬用疫苗来减少发展为进行性感染的犬的数量。在这项研究中,我们在原发性疫苗接种一年后,通过感染性静脉内挑战给予婴儿利什曼原虫前体,观察了最近在欧洲商业化推出的 LiESP/QA-21 犬用疫苗(由婴儿利什曼原虫的分泌/分泌蛋白和 QA-21 皂苷佐剂组成)对选定的体液和细胞免疫参数的影响。我们还跟踪了寄生虫学参数,以确定受挑战犬的寄生虫状况。与对照组相比,尽管受到了致命的挑战,接种疫苗的犬仍然保持了更强的针对寄生虫的细胞介导免疫反应,并且在研究结束时的平均寄生虫负荷明显更低,这与发生活动性感染的可能性降低有关。这些结果证实,LiESP/QA-21 疫苗接种产生的免疫反应在原发性疫苗接种一年后仍然有效,可对抗静脉内挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d72f/4086268/d9ced18ef357/1297-9716-45-69-1.jpg

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