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首页> 外文期刊>Current Drug Targets-Inflammation & Allergy >Design of protective and therapeutic DNA vaccines for the treatment of allergic diseases.
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Design of protective and therapeutic DNA vaccines for the treatment of allergic diseases.

机译:用于治疗变应性疾病的保护性和治疗性DNA疫苗的设计。

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The DNA vaccine revolution has opened a vast scope of novel approaches for protective and therapeutic treatments of type I allergy. This review gives an overview on the current status of allergy DNA vaccines and presents advances in the design of vaccine constructs. An immense number of concurring studies have proven the stimulation of Th1 cells and the induction of a balanced Th1/Th2 cytokine milieu as the fundamental mechanisms underlying the anti-allergic effects of DNA vaccines. Basic vaccine formulations thus can be optimized by improving the cellular immunogenicity via co-administration of cytokines, co-expression or co-application of immunostimulatory DNA sequences or adapting the codon usage. The latter is a frequent and major reason for impaired vaccine expression (e.g. translation of plant allergen genes in mammal cells). Because of unwanted side effects during conventional specific immunotherapy with allergen extracts, safety is increasingly demanded for both, protein and DNA vaccines for allergy treatment. We discuss the creation of hypoallergenic DNA vaccines based on deliberate allergen gene fragmentation, the use of mutations and the routine production of hypoallergenic DNA vaccines by forced ubiquitination. Furthermore, allergen-expressing DNA replicon vaccines are introduced, which enable a drastic reduction of the vaccine dose without loss of anti-allergic efficacy. Finally, the development of DNA multi vaccines and fusion vaccines for protective and therapeutic applications against certain groups of allergens is addressed.
机译:DNA疫苗革命为I型过敏的保护性和治疗性治疗开辟了广阔的范围。这篇综述概述了过敏DNA疫苗的现状,并介绍了疫苗构建体设计的进展。大量的同时研究证明,刺激Th1细胞和诱导平衡的Th1 / Th2细胞因子环境是DNA疫苗抗过敏作用的基本机制。因此,可以通过共同施用细胞因子,共同表达或共同施加免疫刺激性DNA序列或调整密码子使用来改善细胞免疫原性,从而优化基本疫苗制剂。后者是疫苗表达受损(例如,哺乳动物细胞中植物过敏原基因的翻译)受损的常见原因。由于在使用变应原提取物的常规特异性免疫治疗过程中会产生不良副作用,因此对用于变态反应治疗的蛋白质和DNA疫苗的安全性要求越来越高。我们讨论了基于故意变应原基因片段化的低变应原性DNA疫苗的创建,突变的使用以及通过强制泛素化来常规生产低变应原性DNA疫苗。此外,引入了表达变应原的DNA复制子疫苗,其能够大幅度降低疫苗剂量而又不损失抗过敏功效。最后,解决了针对多种过敏原的保护和治疗应用的DNA多疫苗和融合疫苗的开发。

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