Recombinant allergens for diagnosis and therapy of allergic disease

被引:175
作者
Chapman, MD
Smith, AM
Vailes, LD
Arruda, LK
Dhanaraj, V
Pomés, A
机构
[1] Univ Virginia, Asthma & Allerg Dis Ctr, Dept Internal Med, Charlottesville, VA 22908 USA
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Microbiol Immunol & Parasitol, Ribeirao Preto, Brazil
[3] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
关键词
recombinant allergens; mites; animal allergens; allergy diagnostics; allergy therapeutics; asthma; allergy vaccines; allergen immunotherapy;
D O I
10.1067/mai.2000.109832
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Many of the problems associated with using natural allergenic products for allergy diagnosis and treatment can be overcome with use of genetically engineered recombinant allergens. Over the past 10 years, the most important allergens from mites, pollens, animal dander, insects, and foods have been cloned, sequenced, and expressed. In many cases the three-dimensional allergen structure has been determined and B-cell and T-cell epitopes have been mapped. These studies show that allergens have diverse biologic functions (they may be enzymes, enzyme inhibitors, lipocalins, or structural proteins) and that as a rule the allergen function is unrelated to its ability to cause IgE antibody responses, High-level expression systems have been developed to produce recombinant allergens in bacteria, yeast, or insect cells. Recombinant allergens show comparable IgE antibody binding to their natural counterparts (where available) and show excellent reactivity on skin testing and in in vitro diagnostic tests. Cocktails of recombinant allergens can be formulated with predetermined and uniform allergen levels, which could replace natural allergens and result in the development of innovative, patient-based tests for allergy diagnosis. Recombinant allergens also offer the exciting possibility of developing new forms of allergen immunotherapy, including the use of hypoallergens, allergens coupled to IgE suppressive adjuvants, and peptide-based therapies. The production of recombinant allergens as defined molecular entities makes it feasible to consider the possibility of developing prophylactic allergen vaccines. The introduction of recombinant allergens in research and in clinical trials should lead to significant improvements in allergy diagnosis and treatment.
引用
收藏
页码:409 / 418
页数:10
相关论文
共 91 条
  • [21] Flower DR, 1996, BIOCHEM J, V318, P1
  • [22] X-ray and NMR structure of Bet v 1, the origin of birch pollen allergy
    Gajhede, M
    Osmark, P
    Poulsen, FM
    Ipsen, H
    Larsen, JN
    vanNeerven, RJJ
    Schou, C
    Lowenstein, H
    Spangfort, MD
    [J]. NATURE STRUCTURAL BIOLOGY, 1996, 3 (12): : 1040 - 1045
  • [23] Vaccination with heat-killed Listeria as adjuvant reverses established allergen-induced airway hyperreactivity and inflammation:: Role of CD8+ T cells and IL-18
    Hansen, G
    Yeung, VP
    Berry, G
    Umetsu, DT
    DeKruyff, RH
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 164 (01) : 223 - 230
  • [24] Immunoglobulin E-independent major histocompatibility complex-restricted T cell peptide epitope-induced late asthmatic reactions
    Haselden, BM
    Kay, AB
    Larché, M
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (12) : 1885 - 1894
  • [25] A MAJOR HOUSE-DUST MITE ALLERGEN DISRUPTS THE IMMUNOGLOBULIN-E NETWORK BY SELECTIVELY CLEAVING CD23 - INNATE PROTECTION BY ANTIPROTEASES
    HEWITT, CRA
    BROWN, AP
    HART, BJ
    PRITCHARD, DI
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) : 1537 - 1544
  • [26] Strategic targets for primary prevention of allergic disease in childhood
    Holt, PG
    Macaubas, C
    Sly, PD
    [J]. ALLERGY, 1998, 53 : 72 - 76
  • [27] IMMUNOPROPHYLAXIS OF ATOPY - LIGHT AT THE END OF THE TUNNEL
    HOLT, PG
    [J]. IMMUNOLOGY TODAY, 1994, 15 (10): : 484 - 489
  • [28] Ichikawa K, 1999, J ALLERGY CLIN IMMUN, V103, pS184
  • [29] ICHIKAWA K, 2000, IN PRESS INT ARCH AL
  • [30] Jacquet A, 2000, CLIN EXP ALLERGY, V30, P677, DOI 10.1046/j.1365-2222.2000.00823.x