Literature DB >> 24152153

Multiple grass mixes as opposed to single grasses for allergen immunotherapy in allergic rhinitis.

K Gangl1, V Niederberger, R Valenta.   

Abstract

Grass pollen allergy affects approximately 40% of allergic patients. Subcutaneous allergen immunotherapy (SCIT) is the only allergen-specific and disease-modifying treatment available. Currently available therapeutic vaccines for the treatment of grass pollen allergy are based on natural grass pollen extracts which are either made from pollen of one cross-reactive grass species or from several related grass species. Clinical studies have shown that SCIT performed with timothy grass pollen extract is effective for the treatment of grass pollen allergy. Moreover, it has been demonstrated that recombinant timothy grass pollen allergens contain the majority of relevant epitopes and can be used for SCIT in clinical trials. However, recent in vitro studies have suggested that mixes consisting of allergen extracts from several related grass species may have advantages for SCIT over single allergen extracts. Here, we review current knowledge regarding the disease-relevant allergens in grass pollen allergy, available clinical studies comparing SCIT with allergen extracts from timothy grass or from mixes of several related grass species of the Pooideae subfamily, in vitro cross-reactivity studies performed with natural allergen extracts and recombinant allergens and SCIT studies performed with recombinant timothy grass pollen allergens. In vitro and clinical studies performed with natural allergen extracts reveal no relevant advantages of using multiple grass mixes as opposed to single grass pollen extracts. Several studies analysing the molecular composition of natural allergen extracts and the molecular profile of patients' immune responses after SCIT with allergen extracts indicate that the major limitation for the production of a high quality grass pollen vaccine resides in intrinsic features of natural allergen extracts which can only be overcome with recombinant allergen-based technologies.
© 2013 John Wiley & Sons Ltd.

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Year:  2013        PMID: 24152153      PMCID: PMC6624134          DOI: 10.1111/cea.12128

Source DB:  PubMed          Journal:  Clin Exp Allergy        ISSN: 0954-7894            Impact factor:   5.018


  122 in total

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Authors:  Richard W Weber
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Review 2.  Immunological mechanisms of allergen-specific immunotherapy.

Authors:  Mark Larché; Cezmi A Akdis; Rudolf Valenta
Journal:  Nat Rev Immunol       Date:  2006-10       Impact factor: 53.106

Review 3.  Grass pollen, thunderstorms and asthma.

Authors:  R B Knox
Journal:  Clin Exp Allergy       Date:  1993-05       Impact factor: 5.018

4.  Absolute quantification of allergens from complex mixtures: a new sensitive tool for standardization of allergen extracts for specific immunotherapy.

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5.  Generation of an allergy vaccine by disruption of the three-dimensional structure of the cross-reactive calcium-binding allergen, Phl p 7.

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Journal:  J Immunol       Date:  2004-05-01       Impact factor: 5.422

6.  Vaccination with genetically engineered allergens prevents progression of allergic disease.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-13       Impact factor: 11.205

7.  Molecular variability of group 1 and 5 grass pollen allergens between Pooideae species: implications for immunotherapy.

Authors:  H Chabre; B Gouyon; A Huet; V Baron-Bodo; V Boran-Bodo; E Nony; M Hrabina; F Fenaille; A Lautrette; M Bonvalet; B Maillère; V Bordas-Le Floch; L Van Overtvelt; K Jain; E Ezan; T Batard; P Moingeon
Journal:  Clin Exp Allergy       Date:  2009-11-05       Impact factor: 5.018

8.  Molecular characterization of polygalacturonases as grass pollen-specific marker allergens: expulsion from pollen via submicronic respirable particles.

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Journal:  J Immunol       Date:  2004-05-15       Impact factor: 5.422

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  12 in total

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2.  High-density IgE recognition of the major grass pollen allergen Phl p 1 revealed with single-chain IgE antibody fragments obtained by combinatorial cloning.

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3.  Development and characterization of a recombinant, hypoallergenic, peptide-based vaccine for grass pollen allergy.

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Journal:  J Allergy Clin Immunol       Date:  2014-11-13       Impact factor: 10.793

4.  Cell Therapy for Prophylactic Tolerance in Immunoglobulin E-mediated Allergy.

Authors:  Ulrike Baranyi; Andreas M Farkas; Karin Hock; Benedikt Mahr; Birgit Linhart; Martina Gattringer; Margit Focke-Tejkl; Arnd Petersen; Fritz Wrba; Thomas Rülicke; Rudolf Valenta; Thomas Wekerle
Journal:  EBioMedicine       Date:  2016-03-20       Impact factor: 8.143

5.  A B Cell Epitope Peptide Derived from the Major Grass Pollen Allergen Phl p 1 Boosts Allergen-Specific Secondary Antibody Responses without Allergen-Specific T Cell Help.

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Review 6.  Recombinant allergy vaccines based on allergen-derived B cell epitopes.

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7.  A randomized, double-blind, placebo-controlled, dose-finding trial with Lolium perenne peptide immunotherapy.

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Review 8.  Preventive Allergen-Specific Vaccination Against Allergy: Mission Possible?

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Journal:  Front Immunol       Date:  2020-07-07       Impact factor: 7.561

Review 9.  Allergen Extracts for In Vivo Diagnosis and Treatment of Allergy: Is There a Future?

Authors:  Rudolf Valenta; Alexander Karaulov; Verena Niederberger; Yury Zhernov; Olga Elisyutina; Raffaela Campana; Margarete Focke-Tejkl; Mirela Curin; Leyla Namazova-Baranova; Jiu-Yao Wang; Ruby Pawankar; Musa Khaitov
Journal:  J Allergy Clin Immunol Pract       Date:  2018-10-05

10.  Two years of treatment with the recombinant grass pollen allergy vaccine BM32 induces a continuously increasing allergen-specific IgG4 response.

Authors:  Julia Eckl-Dorna; Milena Weber; Victoria Stanek; Birgit Linhart; Robin Ristl; Eva E Waltl; Sergio Villazala-Merino; Andrea Hummel; Margarete Focke-Tejkl; Renate Froeschel; Angela Neubauer; Rainer Henning; Thomas Perkmann; Rudolf Valenta; Verena Niederberger
Journal:  EBioMedicine       Date:  2019-11-28       Impact factor: 8.143

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