Abstract
Allergen immunotherapy (AIT) has been used to treat allergic disease since the early 1900s. Despite numerous clinical trials and meta-analyses proving AIT efficacious, it remains underused and is estimated to be used in less than 10% of patients with allergic rhinitis or asthma worldwide. In addition, there are large differences between regions, which are not only due to socioeconomic status. There is practically no controversy about the use of AIT in the treatment of allergic rhinitis and allergic asthma, but for atopic dermatitis or food allergy, the indications for AIT are not well defined. The elaboration of a wider consensus is of utmost importance because AIT is the only treatment that can change the course of allergic disease by preventing the development of asthma and new allergen sensitizations and by inducing allergen-specific immune tolerance. Safer and more effective AIT strategies are being continuously developed both through elaboration of new allergen preparations and adjuvants and alternate routes of administration. A number of guidelines, consensus documents, or both are available on both the international and national levels. The international community of allergy specialists recognizes the need to develop a comprehensive consensus report to harmonize, disseminate, and implement the best AIT practice. Consequently, the International Collaboration in Asthma, Allergy and Immunology, formed by the European Academy of Allergy and Clinical Immunology; the American Academy of Allergy, Asthma & Immunology; the American College of Allergy, Asthma & Immunology; and the World Allergy Organization, has decided to issue an international consensus on AIT.
Original language | English |
---|---|
Pages (from-to) | 556-568 |
Number of pages | 13 |
Journal | Journal of Allergy and Clinical Immunology |
Volume | 136 |
Issue number | 3 |
DOIs | |
State | Published - 1 Sep 2015 |
Keywords
- International consensus
- allergen vaccine
- allergic rhinitis
- allergy
- asthma
- atopic dermatitis
- food allergy
- immunotherapy
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In: Journal of Allergy and Clinical Immunology, Vol. 136, No. 3, 01.09.2015, p. 556-568.
Research output: Contribution to journal › Review article › peer-review
TY - JOUR
T1 - International consensus on allergy immunotherapy
AU - Jutel, Marek
AU - Agache, Ioana
AU - Bonini, Sergio
AU - Burks, A. Wesley
AU - Calderon, Moises
AU - Canonica, Walter
AU - Cox, Linda
AU - Demoly, Pascal
AU - Frew, Antony J.
AU - O'Hehir, Robin
AU - Kleine-Tebbe, Jörg
AU - Muraro, Antonella
AU - Lack, Gideon
AU - Larenas, Désirée
AU - Levin, Michael
AU - Nelson, Harald
AU - Pawankar, Ruby
AU - Pfaar, Oliver
AU - Van Ree, Ronald
AU - Sampson, Hugh
AU - Santos, Alexandra F.
AU - Du Toit, George
AU - Werfel, Thomas
AU - Gerth Van Wijk, Roy
AU - Zhang, Luo
AU - Akdis, Cezmi A.
N1 - Funding Information: Disclosure of potential conflict of interest: M. Jutel has received research support from the Polish National Science Centre and lecture fees from Allergopharma and Stallergenes. S. Bonini has provided expert testimony for the European Medicines Agency. A. W. Burks is on the FARE and World Allergy Organization boards; is on the Murdoch Children's Research Institute advisory board; has received consultancy fees from Gerson Lehrman Group, ActoGeniX, Genentech, Sanofi US, Valeant Pharmaceuticals North America; has provided unpaid consultation for Dynavax Technologies, Perrigo Company (PBN Nutritionals), and Perosphere; is employed by the University of North Carolina; has patents (US5558869, US55973121, US6441142, US6486311, US6835824, US7485708, and US7879977); has received payment for developing educational presentations from Current Views 2012; and has stock/stock options in Allertein and Mastcell Pharmaceuticals. M. Calderon has received consultancy fees from ALK-Abelló, STG, and Hal Allergy; has received lecture fees from ALK-Abelló STG, and Allergopharma; and has received travel support from ALK-Abelló, STG, Allergopharma, and Hal Allergy. W. Canonica has received consulting fees from ALK-Abelló, Allergy Therapeutics, Lofarma, and Stallergenes. L. Cox has received consulting fees from Greer, has received fees for participation in review activities from Circassia and Biomay, is on the American Board of Allergy and Immunology and American Academy of Allergy, Asthma & Immunology Boards, and has received lecture fees from Southeastern Allergy Asthma Immunology Association. P. Demoly has received consultancy fees from ALK-Abelló, Circassia, Stallergenes, Allergopharma, Thermo Fisher Scientific, DBV, Chiesi, and Pierre Febre Medicaments and has received lecture fees from Menarini, MSD, AstraZeneca, and GlaxoSmithKline. J. Kleine-Tebbe is on the ALK-Abelló, Novartis, Leti, and Bencard advisory boards; has received consultancy fees from Merck and Circassia; has received research support from Circassia; and has received lecture fees from Allergopharma, ALK-Abelló, Bencard, HAL Allergy, LETI, Lofarma, Novartis, and Stallergenes. A. Muraro has received consultancy fees from Meda, Nutricia, Allergopharma, and Novartis. G. Lack has stock/stock options in DBV Technologies. D. Larenas is on the CMICA board; has received consultancy fees from Meda, Pfizer, MIT, Boehringer Ingelheim, Novartis, and Glenmark; has received research support from Novartis, Pfizer, Meda, UCB, GlaxoSmithKline, AstraZeneca, Sunovion, Sanofi, MSD, Teva, and Commet; has received lecture fees from AstraZeneca, Glenmark, MSD, UCB, Meda, and Pfizer; has received payment for developing educational presentations from Glenmark; and has received travel support from MSD, UCB, AstraZeneca, Pfizer, Meda, Senosiain, Glenmark, ALK-Abelló, Novartis, and Chiesi. H. Nelson is on the advisory board for Merck and Circassia, is on the data monitoring board for AstraZeneca and Pearl Therapeutics, and has received research support from Circassia. O. Pfaar has received consultancy fees from Bencard (Germany), HAL-Allergy (The Netherlands), Novartis/LETI (Germany), MEDA (Germany), ALK-Abelló (Germany/Denmark), Allergopharma (Germany), Biotech Tools s.a. (Belgium), GfK Bridgehead (United Kingdom), NAVIGANT-consulting (United States), Sanofi (United States), Guidepoint Global Advisors (United States), Stallergenes (Germany/France), and Mobile Chamber Experts (MCX), a GA2LEN Partner (Germany); is employed by Universitätsmedizin Mannheim, Heidelberg University; has received research support from ALK-Abelló (Germany/Denmark), Allergopharma (Germany), Stallergenes (Germany/France), HAL-Allergy (Germany/The Netherlands), Artu Biologicals (The Netherlands), Allergy Therapeutics/Bencard (UK/Germany), Hartington (Spain), Lofarma (Italy), Novartis/Leti (Germany/Spain), GlaxoSmithKline (United Kingdom/Germany), Essex-Pharma (Germany), Cytos (Switzerland), Curalogic (Denmark), Roxall (Germany), Biomay (Austria), Thermo Fisher (Germany), Circassia (UK), E.U (FP-7-Health-2013-Innovation 1), Biotech Tools s.a. (Belgium), and MEDA-Pharma GmbH (Germany); has received lecture fees from ALK-Abelló (Germany/Denmark), Allergopharma (Germany), Stallergenes (Germany/France), HAL-Allergy (Germany/The Netherlands), Allergy Therapeutics/Bencard (United Kingdom/Germany), Hartington (Spain), Lofarma (Italy), Novartis/Leti (Germany/Spain), GlaxoSmithKline (United Kingdom/Germany), Roxall (Germany), Thermo Fisher (Germany), and MEDA-Pharma GmbH (Germany); is coeditor and author of textbook “Allergien bei Kindern und Jugendlichen” (Schattauer, Germany), author of different chapters of “Allergologie-Handbuch” (Schattauer, Germany), and author of 1 chapter in “Allergologie” (Springer, Germany); has received payment for developing educational presentations from GlaxoSmithKline (Germany), Bencard (Germany), and Novartis (Germany); has received travel support from HAL-Allergy (Netherlands/Germany) and Allergopharma (Germany); and is current chairman of IT IG of European Academy of Allergy and Clinical Immunology (EAACI), and current secretary of ENT-section of DGAKI. R. van Ree is on the EAACI board, has received consultancy fees from HAL Allergy BV, has received research support from the European Union, and has received lecture fees from Thermo Fisher Scientific. H. Sampson is an unpaid consultant on the DBV Scientific Advisory Board. G. Du Toit has received lecture fees from Thermo Fisher, owns 2% equity of the FoodMaestro app, and has received travel support from the EAACI as secretary of the paediatric section. R. Gerth van Wijk has received consultancy fees from MSD, HAL, Crucell, ALK-Abelló, and Novartis; has received research support from NWO, STW, Novartis, Biomay, and DBV; has received lecture fees from Allergopharma and Thermo Fisher; has received payment for manuscript preparation from Chiesi; and receives royalties from de Tijdstroom and Bohn, Stafleu, van Loghum. C. A. Akdis has received consultancy fees from Actellion, Aventis, Stallergenes, Allergopharma, and Circacia; is employed by the Swiss Institute of Allergy and Asthma Research, University of Zuurich; has received research support from Novartis, PREDICTA, Swiss National Science Foundation, MeDALL (Programme no. 261357), and the Christine-Kuhne Center for Allergy Research and Education. The rest of the authors declare that they have no relevant conflicts of interest. Publisher Copyright: © 2015 American Academy of Allergy, Asthma & Immunology.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - Allergen immunotherapy (AIT) has been used to treat allergic disease since the early 1900s. Despite numerous clinical trials and meta-analyses proving AIT efficacious, it remains underused and is estimated to be used in less than 10% of patients with allergic rhinitis or asthma worldwide. In addition, there are large differences between regions, which are not only due to socioeconomic status. There is practically no controversy about the use of AIT in the treatment of allergic rhinitis and allergic asthma, but for atopic dermatitis or food allergy, the indications for AIT are not well defined. The elaboration of a wider consensus is of utmost importance because AIT is the only treatment that can change the course of allergic disease by preventing the development of asthma and new allergen sensitizations and by inducing allergen-specific immune tolerance. Safer and more effective AIT strategies are being continuously developed both through elaboration of new allergen preparations and adjuvants and alternate routes of administration. A number of guidelines, consensus documents, or both are available on both the international and national levels. The international community of allergy specialists recognizes the need to develop a comprehensive consensus report to harmonize, disseminate, and implement the best AIT practice. Consequently, the International Collaboration in Asthma, Allergy and Immunology, formed by the European Academy of Allergy and Clinical Immunology; the American Academy of Allergy, Asthma & Immunology; the American College of Allergy, Asthma & Immunology; and the World Allergy Organization, has decided to issue an international consensus on AIT.
AB - Allergen immunotherapy (AIT) has been used to treat allergic disease since the early 1900s. Despite numerous clinical trials and meta-analyses proving AIT efficacious, it remains underused and is estimated to be used in less than 10% of patients with allergic rhinitis or asthma worldwide. In addition, there are large differences between regions, which are not only due to socioeconomic status. There is practically no controversy about the use of AIT in the treatment of allergic rhinitis and allergic asthma, but for atopic dermatitis or food allergy, the indications for AIT are not well defined. The elaboration of a wider consensus is of utmost importance because AIT is the only treatment that can change the course of allergic disease by preventing the development of asthma and new allergen sensitizations and by inducing allergen-specific immune tolerance. Safer and more effective AIT strategies are being continuously developed both through elaboration of new allergen preparations and adjuvants and alternate routes of administration. A number of guidelines, consensus documents, or both are available on both the international and national levels. The international community of allergy specialists recognizes the need to develop a comprehensive consensus report to harmonize, disseminate, and implement the best AIT practice. Consequently, the International Collaboration in Asthma, Allergy and Immunology, formed by the European Academy of Allergy and Clinical Immunology; the American Academy of Allergy, Asthma & Immunology; the American College of Allergy, Asthma & Immunology; and the World Allergy Organization, has decided to issue an international consensus on AIT.
KW - International consensus
KW - allergen vaccine
KW - allergic rhinitis
KW - allergy
KW - asthma
KW - atopic dermatitis
KW - food allergy
KW - immunotherapy
UR - http://www.scopus.com/inward/record.url?scp=84941192682&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2015.04.047
DO - 10.1016/j.jaci.2015.04.047
M3 - Review article
C2 - 26162571
AN - SCOPUS:84941192682
SN - 0091-6749
VL - 136
SP - 556
EP - 568
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 3
ER -