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
  • [1] IMMUNOCHEMICAL CHARACTERIZATION OF RECOMBINANT AND NATIVE TROPOMYOSINS AS A NEW ALLERGEN FROM THE HOUSE-DUST MITE, DERMATOPHAGOIDES-FARINAE
    AKI, T
    KODAMA, T
    FUJIKAWA, A
    MIURA, K
    SHIGETA, S
    WADA, T
    JYO, T
    MUROOKA, Y
    OKA, S
    ONO, K
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1995, 96 (01) : 74 - 83
  • [2] [Anonymous], 1997, J ALLERGY CLIN IMMUN, V99, P583
  • [3] Cloning of cockroach allergen, Bla g 4, identifies ligand binding proteins (or calycins) as a cause of IgE antibody responses
    Arruda, LK
    Vailes, LD
    Hayden, ML
    Benjamin, DC
    Chapman, MD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (52) : 31196 - 31201
  • [4] MOLECULAR-CLONING OF A MAJOR COCKROACH (BLATTELLA-GERMANICA) ALLERGEN, BLA-G-2 - SEQUENCE HOMOLOGY TO THE ASPARTIC PROTEASES
    ARRUDA, LK
    VAILES, LD
    MANN, BJ
    SHANNON, J
    FOX, JW
    VEDVICK, TS
    HAYDEN, ML
    CHAPMAN, MD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (33) : 19563 - 19568
  • [5] ARRUDA LK, 1999, ALLERGY CLIN IMMUNOL, V11, P167
  • [6] Sequencing and high level expression in Escherichia coli of the tropomyosin allergen (Der p 10) from Dermatophagoides pteronyssinus
    Asturias, JA
    Arilla, MC
    Gómez-Bayón, N
    Martínez, A
    Martínez, J
    Palacios, R
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1397 (01): : 27 - 30
  • [7] GenBank
    Benson, DA
    Karsch-Mizrachi, I
    Lipman, DJ
    Ostell, J
    Rapp, BA
    Wheeler, DL
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (01) : 15 - 18
  • [8] A recombinant house dust mite (HDM) allergen, rDer f 1, with IgE-binding activity comparable to the native allergen
    Best, EA
    Stedman, KE
    Bozic, CM
    Hunter, SW
    Vailes, LD
    Chapman, MD
    McCall, C
    McDermott, MJ
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (01) : S168 - S169
  • [9] PHEROMONE BINDING TO 2 RODENT URINARY PROTEINS REVEALED BY X-RAY CRYSTALLOGRAPHY
    BOCSKEI, Z
    GROOM, CR
    FLOWER, DR
    WRIGHT, CE
    PHILLIPS, SEV
    CAVAGGIONI, A
    FINDLAY, JBC
    NORTH, ACT
    [J]. NATURE, 1992, 360 (6400) : 186 - 188
  • [10] Bousquet J., 1998, Allergy (Copenhagen), V53, P1