Literature DB >> 17305564

Epitope peptides and immunotherapy.

Soichi Tanabe1.   

Abstract

Allergic diseases affect atopic individuals, who synthesize specific Immunoglobulins E (IgE) to environmental allergens, usually proteins or glycoproteins. These allergens include grass and tree pollens, indoor allergens such as house dust mites and animal dander, and various foods. Because allergen-specific IgE antibodies are the main effector molecules in the immune response to allergens, many studies have focused on the identification of IgE-binding epitopes (called B cell epitopes), specific and minimum regions of allergen molecules that binds to IgE. Our initial studies have provided evidence that only four to five amino acid residues are enough to comprise an epitope, since pentapeptide QQQPP in wheat glutenin is minimally required for IgE binding. Afterwards, various kinds of B cell epitope structures have been clarified. Such information contributes greatly not only to the elucidation of the etiology of allergy, but also to the development of strategies for the treatment and prevention of allergy. Allergen-specific T cells also play an important role in allergy and are obvious targets for intervention in the disease. Currently, the principle approach is to modify B cell epitopes to prevent IgE binding while preserving T cell epitopes to retain the capacity for immunotherapy. There is mounting evidence that the administration of peptide(s) containing immunodominant T cell epitopes from an allergen can induce T cell nonresponsiveness (immunotherapy). There have been clinical studies of peptide immunotherapy performed, the most promising being for bee venom sensitivity. Clinical trials of immunotherapy for cat allergen peptide have also received attention. An alternative strategy for the generation of an effective but hypoallergenic preparation for immunotherapy is to modify T cell epitope peptides by, for example, single amino acid substitution. In this article, I will present an overview of epitopes related to allergic disease, particularly stress on allergen specific immunotherapy. In addition, our ongoing study of immunotherapy by 'eating' T cell epitope peptides will be described. Eating T cell epitope peptides as food provides a more practical way of inducing tolerance and a challenge to prevent allergy in daily life, as opposed to therapy by ingesting peptides as medicine.

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Year:  2007        PMID: 17305564     DOI: 10.2174/138920307779941569

Source DB:  PubMed          Journal:  Curr Protein Pept Sci        ISSN: 1389-2037            Impact factor:   3.272


  15 in total

1.  Designer covalent heterobivalent inhibitors prevent IgE-dependent responses to peanut allergen.

Authors:  Peter E Deak; Baksun Kim; Amina Abdul Qayum; Jaeho Shin; Girish Vitalpur; Kirsten M Kloepfer; Matthew J Turner; Neal Smith; Wayne G Shreffler; Tanyel Kiziltepe; Mark H Kaplan; Basar Bilgicer
Journal:  Proc Natl Acad Sci U S A       Date:  2019-04-08       Impact factor: 11.205

2.  Design of a heterotetravalent synthetic allergen that reflects epitope heterogeneity and IgE antibody variability to study mast cell degranulation.

Authors:  Michael W Handlogten; Tanyel Kiziltepe; Basar Bilgicer
Journal:  Biochem J       Date:  2013-01-01       Impact factor: 3.857

Review 3.  Peptides and peptidomimetics as immunomodulators.

Authors:  Ameya S Gokhale; Seetharama Satyanarayanajois
Journal:  Immunotherapy       Date:  2014       Impact factor: 4.196

4.  Synthetic allergen design reveals the significance of moderate affinity epitopes in mast cell degranulation.

Authors:  Michael W Handlogten; Tanyel Kiziltepe; Nathan J Alves; Basar Bilgicer
Journal:  ACS Chem Biol       Date:  2012-08-21       Impact factor: 5.100

Review 5.  Novel approaches to food allergy.

Authors:  Yao-Hsu Yang; Bor-Luen Chiang
Journal:  Clin Rev Allergy Immunol       Date:  2014-06       Impact factor: 8.667

Review 6.  Immunoglobulin E-binding epitopes of mite allergens: from characterization to immunotherapy.

Authors:  Yubao Cui
Journal:  Clin Rev Allergy Immunol       Date:  2014-12       Impact factor: 8.667

7.  Inhibition of weak-affinity epitope-IgE interactions prevents mast cell degranulation.

Authors:  Michael W Handlogten; Tanyel Kiziltepe; Ana P Serezani; Mark H Kaplan; Basar Bilgicer
Journal:  Nat Chem Biol       Date:  2013-10-06       Impact factor: 15.040

8.  An expanded self-antigen peptidome is carried by the human lymph as compared to the plasma.

Authors:  Cristina C Clement; Elvira S Cannizzo; Maria-Dorothea Nastke; Ranjit Sahu; Waldemar Olszewski; Norman E Miller; Lawrence J Stern; Laura Santambrogio
Journal:  PLoS One       Date:  2010-03-26       Impact factor: 3.240

9.  Nanoallergens: A multivalent platform for studying and evaluating potency of allergen epitopes in cellular degranulation.

Authors:  Peter E Deak; Maura R Vrabel; Vincenzo J Pizzuti; Tanyel Kiziltepe; Basar Bilgicer
Journal:  Exp Biol Med (Maywood)       Date:  2016-04-13

Review 10.  Strategies to query and display allergy-derived epitope data from the immune epitope database.

Authors:  Kerrie Vaughan; Bjoern Peters; Mark Larche; Anna Pomes; David Broide; Alessandro Sette
Journal:  Int Arch Allergy Immunol       Date:  2012-11-21       Impact factor: 2.749

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