Hartl A, Hochreiter R, Stepanoska T, Ferreira F, Thalhamer J
Institute of Chemistry and Biochemistry, University of Salzburg, Salzburg, Austria.
Allergy. 2004 Jan;59(1):65-73. doi: 10.1046/j.1398-9995.2003.00335.x.
An estimated 100 million individuals suffer from birch pollen allergy. More than 95% of birch pollen-allergic subjects react with the major birch pollen allergen Bet v 1a, and almost 60% of them are sensitized exclusively to this allergen.
DNA immunization using the Bet v 1a gene was evaluated with respect to its prophylactic and therapeutic efficacy.
A DNA vaccine containing the entire Bet v 1a cDNA under the control of a CMV-promoter was constructed. In order to estimate the protective efficiency, animals received three injections of this vaccine prior to sensitization with recombinant Bet v 1a. Vice versa, in a therapeutic approach, sensitization was followed by treatment with the DNA vaccine.
The Bet v 1a DNA vaccine induced strong Bet v 1-specific antibody responses with a Th1-biased response type. Animals which received the DNA vaccine were protected against a following allergic sensitization with Bet v 1a. The protective effect was characterized by suppression of Bet v 1-specific immunoglobulin (Ig)E production, lack of basophil activation and enhanced interferon (IFN)-gamma expression. In a therapeutic situation, treatment of sensitized animals with DNA vaccines decreased IgE production, IgE-mediated basophil release and drastically reduced anaphylactic activity as measured by passive cutaneous anaphylaxis assays. Concerning the cellular immune response, DNA immunization induced a sustaining and dominant shift from a Th2 type response towards a balanced Th1/Th2 type response as indicated by increased IFN-gamma but unchanged IL-5 levels in lymphoproliferation assays.
The results demonstrate the allergen-specific protective and therapeutic efficacy of a DNA vaccine encoding the clinically highly relevant allergen Bet v 1a indicating the suitability of this concept for the treatment of allergic diseases.
估计有1亿人患有桦树花粉过敏症。超过95%的桦树花粉过敏患者对主要的桦树花粉过敏原Bet v 1a产生反应,其中近60%的人仅对该过敏原敏感。
评估使用Bet v 1a基因进行DNA免疫的预防和治疗效果。
构建了一种在巨细胞病毒(CMV)启动子控制下包含完整Bet v 1a cDNA的DNA疫苗。为了评估保护效率,在动物用重组Bet v 1a致敏前给予三次该疫苗注射。反之,在治疗方法中,致敏后用DNA疫苗进行治疗。
Bet v 1a DNA疫苗诱导了强烈的Bet v 1特异性抗体反应,反应类型偏向Th1型。接受DNA疫苗的动物对随后的Bet v 1a过敏致敏具有保护作用。保护作用的特征是抑制Bet v 1特异性免疫球蛋白(Ig)E的产生、嗜碱性粒细胞无活化以及干扰素(IFN)-γ表达增强。在治疗情况下,用DNA疫苗治疗致敏动物可降低IgE产生、IgE介导的嗜碱性粒细胞释放,并通过被动皮肤过敏试验显著降低过敏活性。关于细胞免疫反应,DNA免疫诱导了从Th2型反应向平衡的Th1/Th2型反应的持续且占主导的转变,这在淋巴细胞增殖试验中表现为IFN-γ水平升高但IL-5水平不变。
结果证明了编码临床上高度相关过敏原Bet v 1a的DNA疫苗具有过敏原特异性的保护和治疗效果,表明该概念适用于治疗过敏性疾病。