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
相关论文
共 68 条
[1]   Role of interleukin 10 in specific immunotherapy [J].
Akdis, CA ;
Blesken, T ;
Akdis, M ;
Wüthrich, B ;
Blaser, K .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (01) :98-106
[2]   Regulation of specific immune responses by chemical and structural modifications of allergens [J].
Akdis, CA ;
Blaser, K .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2000, 121 (04) :261-269
[3]  
Akdis CA, 1998, EUR J IMMUNOL, V28, P914, DOI 10.1002/(SICI)1521-4141(199803)28:03<914::AID-IMMU914>3.0.CO
[4]  
2-C
[5]   Immunologic mechanisms of specific immunotherapy [J].
Akdis, CA ;
Blaser, K .
ALLERGY, 1999, 54 :31-32
[6]   Mechanisms of allergen-specific immunotherapy [J].
Akdis, CA ;
Blaser, K .
ALLERGY, 2000, 55 (06) :522-530
[7]   Biological features of genetic immunization [J].
Barry, MA ;
Johnston, SA .
VACCINE, 1997, 15 (08) :788-791
[8]   Hypoallergenic variants of the Parietaria judaica major allergen Par j 1:: A member of the non-specific lipid transfer protein plant family [J].
Bonura, A ;
Amoroso, S ;
Locorotondo, G ;
Di Felice, G ;
Tinghino, R ;
Geraci, D ;
Colombo, P .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 126 (01) :32-40
[9]   Allergen immunotherapy:: therapeutic vaccines for allergic diseases [J].
Bousquet, J ;
Lockey, R ;
Malling, HJ ;
Alvarez-Cuesta, E ;
Canonica, GW ;
Chapman, MD ;
Creticos, PJ ;
Dayer, JM ;
Durham, SR ;
Demoly, P ;
Goldstein, RJ ;
Ishikawa, T ;
Ito, K ;
Kraft, D ;
Lambert, PH ;
Lowenstein, H ;
Müller, U ;
Norman, PS ;
Reisman, RE ;
Valenta, R ;
Valovirta, E ;
Yssel, H .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 1998, 81 (05) :401-405
[10]   4 RECOMBINANT ISOFORMS OF COR ALPHA-I, THE MAJOR ALLERGEN OF HAZEL POLLEN, SHOW DIFFERENT IGE-BINDING PROPERTIES [J].
BREITENEDER, H ;
FERREIRA, F ;
HOFFMANNSOMMERGRUBER, K ;
EBNER, C ;
BREITENBACH, M ;
RUMPOLD, H ;
KRAFT, D ;
SCHEINER, O .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 212 (02) :355-362