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Review
. 2017;172(4):187-202.
doi: 10.1159/000464104. Epub 2017 May 4.

Recombinant Allergens in Structural Biology, Diagnosis, and Immunotherapy

Affiliations
Review

Recombinant Allergens in Structural Biology, Diagnosis, and Immunotherapy

Angelika Tscheppe et al. Int Arch Allergy Immunol. 2017.

Abstract

The years 1988-1995 witnessed the beginning of allergen cloning and the generation of recombinant allergens, which opened up new avenues for the diagnosis and research of human allergic diseases. Most crystal and solution structures of allergens have been obtained using recombinant allergens. Structural information on allergens allows insights into their evolutionary biology, illustrates clinically observed cross-reactivities, and makes the design of hypoallergenic derivatives for allergy vaccines possible. Recombinant allergens are widely used in molecule-based allergy diagnosis such as protein microarrays or suspension arrays. Recombinant technologies have been used to produce well-characterized, noncontaminated vaccine components with known biological activities including a variety of allergen derivatives with reduced IgE reactivity. Such recombinant hypoallergens as well as wild-type recombinant allergens have been used successfully in several immunotherapy trials for more than a decade to treat birch and grass pollen allergy. As a more recent application, the development of antibody repertoires directed against conformational epitopes during immunotherapy has been monitored by recombinant allergen chimeras. Although much progress has been made, the number and quality of recombinant allergens will undoubtedly increase and keep improving our knowledge in basic scientific investigations, diagnosis, and therapy of human allergic diseases.

Keywords: Allergy diagnosis; Allergy immunotherapy; Clinical studies; Recombinant allergens; Structural biology; Vaccine development.

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References

    1. Chua KY, Stewart GA, Thomas WR, Simpson RJ, Dilworth RJ, Plozza TM, Turner KJ. Sequence analysis of cDNA coding for a major house dust mite allergen, Der p 1. Homology with cysteine proteases. J Exp Med. 1988;167:175–182. - PMC - PubMed
    1. Thomas WR, Stewart GA, Simpson RJ, Chua KY, Plozza TM, Dilworth RJ, Nisbet A, Turner KJ. Cloning and expression of DNA coding for the major house dust mite allergen Der p 1 in Escherichia coli. Int Arch Allergy Appl Immunol. 1988;85:127–129. - PubMed
    1. Fang KS, Vitale M, Fehlner P, King TP. cDNA cloning and primary structure of a white-face hornet venom allergen, antigen 5. Proc Natl Acad Sci USA. 1988;85:895–899. - PMC - PubMed
    1. Breiteneder H, Pettenburger K, Bito A, Valenta R, Kraft D, Rumpold H, Scheiner O, Breitenbach M. The gene coding for the major birch pollen allergen Bet v 1, is highly homologous to a pea disease resistance response gene. EMBO J. 1989;8:1935–1938. - PMC - PubMed
    1. Breiteneder H, Hassfeld W, Pettenburger K, Jarolim E, Breitenbach M, Rumpold H, Kraft D, Scheiner O. Isolation and characterization of messenger RNA from male inflorescences and pollen of the white birch (Betula verrucosa) Int Arch Allergy Appl Immunol. 1988;87:19–24. - PubMed