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Synthetic peptide vaccines: foot-and-mouth disease virus as a model.

机译:合成肽疫苗:口蹄疫病毒为模型。

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Foot-and-mouth disease virus (FMDV) has been one of the pioneering viral systems in the development of synthetic peptides as vaccines. Protection against FMDV infection is associated with the induction of neutralising antibodies. Therefore, attempts have been made to identify peptides capable of eliciting protective humoral responses. Peptides based on a continuous, immunodominant B cell site on the capsid protein VP1 have been shown to confer limited protection in natural hosts. This probably reflects the difficulties in reproducing the immunogenicity of an entire viral particle by using a much simpler synthetic antigen, due to: (i) the polymorphism of the class II MHC; (ii) the adequate presentation to the immune system of the peptides, and (iii) the difficulties of achieving protection against a highly variable RNA virus, which may favour selection of virus antigenic variants. The improvement of FMD peptide vaccines, and the development of in vitro alternatives to in vivo immunogenic assays require further understanding of the immune mechanisms leading to protection against this important animal virus disease.
机译:口蹄疫病毒(FMDV)已成为开发合成肽疫苗的先锋病毒系统之一。预防FMDV感染与中和抗体的诱导有关。因此,已经尝试鉴定能够引起保护性体液应答的肽。已经显示,基于衣壳蛋白VP1上连续的免疫优势B细胞位点的肽在天然宿主中具有有限的保护作用。这可能反映出由于使用以下更为简单的合成抗原而难以复制整个病毒颗粒的免疫原性的原因:(i)II类MHC的多态性; (ii)肽对免疫系统的适当呈递,以及(iii)难以针对高度可变的RNA病毒提供保护的困难,这可能有利于选择病毒抗原变体。 FMD肽疫苗的改进以及体内免疫原性测定方法的体外替代方法的开发,需要对导致保护免受这种重要动物病毒疾病的免疫机制有进一步的了解。

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