4.7 Review

Facing Hymenoptera Venom Allergy: From Natural to Recombinant Allergens

Journal

TOXINS
Volume 7, Issue 7, Pages 2551-2570

Publisher

MDPI
DOI: 10.3390/toxins7072551

Keywords

Hymenoptera venom; allergy; recombinant allergens; omics approaches; diagnosis; immunotherapy

Funding

  1. FAPESP (Sao Paulo Research Foundation) [2014/13936-7, 2009/51539-1]
  2. Prope-UNESP (Pro Reitoria da Universidade Estadual Paulista, SP) [10/2014]
  3. Programa de Internacionalizacao da Pesquisa da UNESP [Prope-PROINTER-UNESP-04/2015]
  4. FUNDUNESP-UNESP (Fundacao para o Desenvolvimento da Universidade Estadual Paulista, SP, Brazil) [Proc. 0119710]
  5. CAPES-DS (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior), Post-Graduation Program of Biological Sciences (Cellular and Molecular Biology) at UNESP, Rio Claro

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Along with food and drug allergic reactions, a Hymenoptera insect Sting (Apoidea, Vespidae, Formicidae) is one of the most common causes of anaphylaxis worldwide. Diagnoses of Hymenoptera venom allergy (HVA) and specific immunotherapy (SIT) have been based on the use of crude venom extracts. However, the incidence of cross-reactivity and low levels of sensibility during diagnosis, as well as the occurrence of nonspecific sensitization and undesired side effects during SIT, encourage the search for novel allergenic materials. Recombinant allergens are an interesting approach to improve allergy diagnosis and SIT because they circumvent major problems associated with the use of crude venom. Production of recombinant allergens depends on the profound molecular characterization of the natural counterpart by combining some omics approaches with high-throughput screening techniques and the selection of an appropriate system for heterologous expression. To date, several clinically relevant allergens and novel venom toxins have been identified, cloned and characterized, enabling a better understanding of the whole allergenic and envenoming processes. Here, we review recent findings on identification, molecular characterization and recombinant expression of Hymenoptera venom allergens and on the evaluation of these heterologous proteins as valuable tools for tackling remaining pitfalls on HVA diagnosis and immunotherapy.

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