Literature DB >> 26013124

Current developments for improving efficacy of allergy vaccines.

Alessandra Sandrini1, Jennifer M Rolland, Robyn E O'Hehir.   

Abstract

Allergic diseases are prevalent worldwide. Allergen immunotherapy (AIT) is a current treatment for allergy, leading to modification of the natural course of disease. Mechanisms of efficacy include Treg through release of IL-10 and TGF-β and specific IgG4 blocking antibodies. Subcutaneous and sublingual routes are popular, but uptake is limited by inconvenience and safety concerns. Inclusion criteria limit application to a small proportion of allergic patients. New forms of immunotherapy are being investigated for more efficacious, convenient and safer options with promising advances in recent years. The rationale of reducing vaccine allergenicity to increase safety while improving immunogenicity led to investigation of T-cell epitope-based peptides and recombinant allergen derivatives. Additionally, different routes of administration and adjuvants and adjunct therapies are being explored. This review discusses the current status of AIT and recent advances to improve clinical efficacy, safety and long-term immune tolerance.

Entities:  

Keywords:  T-cell anergy; T-cell epitope peptide; Treg; adjuvant; allergen immunotherapy; allergic rhinitis; allergy vaccine; asthma; recombinant allergen; sublingual immunotherapy

Mesh:

Substances:

Year:  2015        PMID: 26013124     DOI: 10.1586/14760584.2015.1050385

Source DB:  PubMed          Journal:  Expert Rev Vaccines        ISSN: 1476-0584            Impact factor:   5.217


  7 in total

1.  Allergen-encoding bone marrow transfer inactivates allergic T cell responses, alleviating airway inflammation.

Authors:  Jane Al-Kouba; Andrew N Wilkinson; Malcolm R Starkey; Rajeev Rudraraju; Rhiannon B Werder; Xiao Liu; Soi-Cheng Law; Jay C Horvat; Jeremy F Brooks; Geoffrey R Hill; Janet M Davies; Simon Phipps; Philip M Hansbro; Raymond J Steptoe
Journal:  JCI Insight       Date:  2017-06-02

Review 2.  Nanoparticle-allergen complexes for allergen immunotherapy.

Authors:  Gabriella Di Felice; Paolo Colombo
Journal:  Int J Nanomedicine       Date:  2017-06-19

3.  Subcutaneous immunotherapy using modified Phl p5a-derived peptides efficiently alleviates allergic asthma in mice.

Authors:  Laura Hesse; Roy Feenstra; Martino Ambrosini; Wim A de Jager; Arjen Petersen; Henk Vietor; Wendy W J Unger; Yvette van Kooyk; Martijn C Nawijn
Journal:  Allergy       Date:  2019-07-08       Impact factor: 13.146

Review 4.  T Cell Epitope Peptide Therapy for Allergic Diseases.

Authors:  Robyn E O'Hehir; Sara R Prickett; Jennifer M Rolland
Journal:  Curr Allergy Asthma Rep       Date:  2016-02       Impact factor: 4.806

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.  Effect of Heat Processing on IgE Reactivity and Cross-Reactivity of Tropomyosin and Other Allergens of Asia-Pacific Mollusc Species: Identification of Novel Sydney Rock Oyster Tropomyosin Sac g 1.

Authors:  Jennifer M Rolland; Nirupama P Varese; Jodie B Abramovitch; Jessica Anania; Roni Nugraha; Sandip Kamath; Anita Hazard; Andreas L Lopata; Robyn E O'Hehir
Journal:  Mol Nutr Food Res       Date:  2018-05-14       Impact factor: 5.914

7.  Immunotherapy With the PreS-based Grass Pollen Allergy Vaccine BM32 Induces Antibody Responses Protecting Against Hepatitis B Infection.

Authors:  Carolin Cornelius; Katrin Schöneweis; Fanny Georgi; Milena Weber; Verena Niederberger; Petra Zieglmayer; Katarzyna Niespodziana; Michael Trauner; Harald Hofer; Stephan Urban; Rudolf Valenta
Journal:  EBioMedicine       Date:  2016-08-08       Impact factor: 8.143

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.