Abstract

Purpose of reviewMore than 30 years ago, the first molecular structures of allergens were elucidated and defined recombinant allergens became available. We review the state of the art regarding molecular AIT with the goal to understand why progress in this field has been slow, although there is huge potential for treatment and allergen-specific prevention.Recent findingsOn the basis of allergen structures, several AIT strategies have been developed and were advanced into clinical evaluation. In clinical AIT trials, promising results were obtained with recombinant and synthetic allergen derivatives inducing allergen-specific IgG antibodies, which interfered with allergen recognition by IgE whereas clinical efficacy could not yet be demonstrated for approaches targeting only allergen-specific T-cell responses. Available data suggest that molecular AIT strategies have many advantages over allergen extract-based AIT.SummaryClinical studies indicate that recombinant allergen-based AIT vaccines, which are superior to existing allergen extract-based AIT can be developed for respiratory, food and venom allergy. Allergen-specific preventive strategies based on recombinant allergen-based vaccine approaches and induction of T-cell tolerance are on the horizon and hold promise that allergy can be prevented. However, progress is limited by lack of resources needed for clinical studies, which are necessary for the development of these innovative strategies.

Highlights

  • Immunoglobulin E (IgE)-associated allergy is the most common immunologically mediated hypersensitivity disease world-wide [1&,2,3]

  • In order to obtain a generally applicable method for the production of peptide carrier-based allergen-specific immunotherapy (AIT) vaccines suitable for large-scale Good Manufacturing Practice (GMP) production, we developed recombinant peptide carrier-based vaccines, which are based on recombinant fusion proteins consisting of a nonallergenic carrier protein fused to nonallergenic allergen-derived peptides to induce blocking IgG antibodies with T-cell help from the carrier reducing allergen-derived T-cell epitopes in the vaccine [96,97]

  • The further development of AIT is severely hampered by the quality of natural allergen extracts and can only be achieved with molecular AIT strategies

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Summary

INTRODUCTION

Immunoglobulin E (IgE)-associated allergy is the most common immunologically mediated hypersensitivity disease world-wide [1&,2,3]. The need for detailed diagnosis may be aNRC Institute of Immunology FMBA of Russia, Moscow, Russia, bDiDivision of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria and cLaboratory of Immunopathology, Department of Clinical Immunology and Allergy, Sechenov First Moscow State Medical University, Moscow, Russia.

KEY POINTS
Study design and clinical trial number
CONCLUSION
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