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Poultry Coccidiosis: Design and Interpretation of Vaccine Studies

机译:家禽椰子症:疫苗研究的设计与解释

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Eimeria infection impacts upon chicken welfare and economic productivity of the poultry sector. Live coccidiosis vaccines for chickens have been available for almost 70 years, but the requirement to formulate blends of oocysts from multiple Eimeria species makes vaccine production costly and logistically demanding. A multivalent vaccine that does not require chickens for its production and can induce protection against multiple Eimeria species is highly desirable. However, despite the identification and testing of many vaccine candidate antigens, no recombinant coccidiosis vaccine has been developed commercially. Currently, assessment of vaccine efficacy against Eimeria, and the disease coccidiosis, can be done only through in vivo vaccination and challenge experiments but the design of such studies has been highly variable. Lack of a ‘standard’ protocol for assessing vaccine efficacy makes comparative evaluations very difficult, complicating vaccine development and validation. The formulation and schedule of vaccination, the breed of chicken and choice of husbandry system, the species, strain, magnitude and timing of delivery of the parasite challenge, and the parameters used to assess vaccine efficacy all influence the outcomes of experimental trials. In natural Eimeria infection the induction of strong cell mediated immune responses are central to the development of protective immunity against coccidiosis. Antibodies are generally regarded to be of lesser importance. Unfortunately, there are no specific immunological assays that can accurately predict how well a vaccine will protect against coccidiosis (i.e. no ‘correlates of protection’). Thus experimental vaccine studies rely on assessing a variety of post-challenge parameters, including assessment of pathognomonic lesions, measurements of parasite replication such as oocyst output or quantification of Eimeria genomes, and/or measurements of productivity such as body weight gain and feed conversion rates. Understanding immune responses to primary and secondary infection can inform on the most appropriate immunological assays. The discovery of new antigens for different Eimeria species and the development of new methods of vaccine antigen delivery necessitates a more considered approach to assessment of novel vaccines with robust, repeatable study design. Careful consideration of performance and welfare factors that are genuinely relevant to chicken producers and vaccine manufacturers is essential.
机译:Eimeria感染对家禽部门的养鸡福利和经济生产力的影响。鸡的活椰子疫苗疫苗已经可用近70年,但要求从多个eimeria种类的卵囊配制卵囊混合物使疫苗生产昂贵和逻辑苛刻。一种不需要鸡的多价疫苗,可以非常理想地诱导对多个Eimeria物种的保护。然而,尽管对许多疫苗候选抗原的鉴定和测试,但在商业上没有开发重组椰子病疫苗。目前,疫苗疗效评估对艾美氏症,以及疾病球虫病,只能通过体内疫苗接种和挑战实验进行,但这些研究的设计具有高度变化。缺乏“标准”评估疫苗疗效的协议使比较评估非常困难,疫苗发育和验证使其变得复杂化。疫苗接种的配方和时间表,养鸡和饲养系统的选择,物种,菌株,递送寄生虫挑战的时间,以及用于评估疫苗疗效的参数都影响了实验试验的结果。在天然的eimeria感染中,强细胞介导的免疫反应的诱导是对椰子症的保护性免疫发育的核心。抗体通常被认为具有较小的重要性。不幸的是,没有具体的免疫测定可以准确地预测疫苗将如何保护免受椰子症(即没有“的保护”)。因此,实验疫苗研究依赖于评估各种攻击后参数,包括评估病例病变,寄生虫复制的测量,例如卵囊产量或eimeria基因组的定量,以及生产率,如体重增加和饲料转化率的生产率。了解对初级和继发感染的免疫应答可以通知最适当的免疫学测定。对不同eimeria种类的新抗原的发现以及新方法的疫苗抗原递送的发展需要更加考虑具有鲁棒,可重复的研究设计的新型疫苗的方法。仔细考虑与鸡生产商和疫苗制造商真正相关的表现和福利因素至关重要。

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