Literature DB >> 29205109

New Treatments for Allergy: Advances in Peptide Immunotherapy.

David Calzada1, Selene Baos1, Lucia Cremades1, Blanca Cardaba1,2.   

Abstract

BACKGROUND: Nowadays, allergen-specific immunotherapy (AIT) is the only treatment able to modulate the course of allergic diseases. Although it has been applied for the last 100 years, treatment with whole allergen extracts is not without its drawbacks: AIT can cause local and systemic adverse events and may produce new IgE sensitization against other allergens present in the extract. Furthermore, the lengthy treatment duration (3-5 years), frequent administration, and high cost of treatment are other disadvantages. For these reasons, there is a need for safer and more effective AIT strategies. One promising approach is the use of synthetic peptides representing the B- or T-cell epitopes of allergens.
OBJECTIVE: This review summarizes the main advances in peptide immunotherapy, from preclinical models to early clinical trials, focusing on house dust mite, bee venom, cat allergy, and Oleaceae pollinosis.
RESULTS: Following an extensive review of the relevant literature, we summarize how peptide therapies may change the course of allergic diseases and promote allergen tolerance, thereby ameliorating the main disadvantages of AIT. Although the molecular mechanisms involved are not yet fully defined, they seem to depend on structure, length, peptide sequence, and route of administration. This novel immunotherapy has been demonstrated to modulate the immune system, promoting regulatory T-cell induction and Th2 inhibition. This tolerance-inducing potential has led this therapy to be termed SPIRE (synthetic peptide immuno-regulatory epitopes).
CONCLUSION: Experimental models and clinical trials have demonstrated the usefulness of SPIRE treatment to cure these diseases, opening a new era in allergen therapeutics. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Allergy; SPIRE; T-cell epitopes; immunoregulation; peptide immunotherapy; regulatory T cells.

Mesh:

Substances:

Year:  2018        PMID: 29205109     DOI: 10.2174/0929867325666171201114353

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  6 in total

Review 1.  Newly identified T cell subsets in mechanistic studies of food immunotherapy.

Authors:  Vanitha Sampath; Kari C Nadeau
Journal:  J Clin Invest       Date:  2019-04-01       Impact factor: 14.808

2.  Peptides from allergenic lipocalins bind to formyl peptide receptor 3 in human dendritic cells to mediate TH2 immunity.

Authors:  Dominik Klaver; Beate Posch; Anita Geisler; Martin Hermann; Norbert Reider; Christine Heufler
Journal:  J Allergy Clin Immunol       Date:  2019-07-19       Impact factor: 10.793

Review 3.  Allergic Diseases: A Comprehensive Review on Risk Factors, Immunological Mechanisms, Link with COVID-19, Potential Treatments, and Role of Allergen Bioinformatics.

Authors:  Fahad M Aldakheel
Journal:  Int J Environ Res Public Health       Date:  2021-11-18       Impact factor: 3.390

4.  In vivo Induction of Functional Inhibitory IgG Antibodies by a Hypoallergenic Bet v 1 Variant.

Authors:  Lorenz Aglas; Athanasios Bethanis; Paulina Chrusciel; Frank Stolz; Melanie Gruen; Ulla-Marjut Jaakkola; Laurian Jongejan; Emrah Yatkin; Ronald Van Ree
Journal:  Front Immunol       Date:  2020-09-03       Impact factor: 7.561

Review 5.  Immunological Mechanisms in Allergic Diseases and Allergen Tolerance: The Role of Treg Cells.

Authors:  D Calzada; S Baos; L Cremades-Jimeno; B Cárdaba
Journal:  J Immunol Res       Date:  2018-06-14       Impact factor: 4.818

6.  Mechanism(s) of prolonged attenuation of allergic responses after modulation of idiotypic regulatory network.

Authors:  R M Gorczynski; T Maqbool; G Hoffmann
Journal:  Allergy Asthma Clin Immunol       Date:  2019-12-04       Impact factor: 3.406

  6 in total

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