Genetic engineering of allergens: Future therapeutic products

被引:53
作者
Ferreira, F
Wallner, M
Breiteneder, H
Hartl, A
Thalhamer, J
Ebner, C
机构
[1] Salzburg Univ, Inst Genet & Allgemeine Biol, A-5020 Salzburg, Austria
[2] Salzburg Univ, Inst Chem & Biochem, A-5020 Salzburg, Austria
[3] Univ Vienna, Dept Pathophysiol, Vienna, Austria
关键词
allergen; immunotherapy; hypoallergen; genetic engineering; recombinant allergen;
D O I
10.1159/000064249
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Genetic engineering of allergens for specific immunotherapy should aim at the production of modified molecules with reduced IgE-binding epitopes (hypoallergens), while preserving structural motifs necessary for T cell recognition (T cell epitopes) and for induction of IgG antibodies reactive with the natural allergen (blocking antibodies). Common approaches for engineering of hypoallergens usually require knowledge of T and B cell epitopes and involve changing specific base pairs (mutated gene), introduction of a new piece of DNA into the existing DNA molecule (chimeric or hybrid gene), and deletions (truncated gene or fragments). DNA family shuffling has the advantage that it does not require a priori knowledge of structural and functional properties for efficient generation of hypoallergens. The combination of the hypoallergen concept with the Th1-inducing genetic immunization approach might be an attractive alternative for protein-based immunotherapy. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:171 / 178
页数:8
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