TY - JOUR
T1 - Preventive Allergen-Specific Vaccination Against Allergy
T2 - Mission Possible?
AU - Tulaeva, Inna
AU - Kratzer, Bernhard
AU - Campana, Raffaela
AU - Curin, Mirela
AU - van Hage, Marianne
AU - Karsonova, Antonina
AU - Riabova, Ksenja
AU - Karaulov, Alexander
AU - Khaitov, Musa
AU - Pickl, Winfried F
AU - Valenta, Rudolf
N1 - Funding Information:
The authors acknowledge the members of the scientific and clinical development teams who moved BM32 and its components into clinical evaluation. The long-lasting support of the Austrian Science Fund (FWF), Biomay AG, Vienna, Austria, the Christian Doppler Research Association, Austria, the Medical University of Vienna, Austria, and recently of the NRC Institute of Immunology FMBA of Russia, Moscow, Russia, and Sechenov First Moscow State Medical University, Moscow, Russia is acknowledged. Funding. This work was supported by grants F4605, F4609, and DK-IAI, DK-W1248 from the Austrian Science Fund (FWF), by the Sience Fund of the Country of Lower Austria, by the Russian Academic Excellence Project 5-100 and by a Megagrant of the Government of the Russian Federation (Grant No. 14.W03.31.0024). In addition funding from The Region Stockholm ALF project, the Swedish Asthma and Allergy Research Foundation, the Swedish Heart-Lung Foundation, the Cancer- and Allergy Foundation and the Swedish Research Council is acknowledged.
Publisher Copyright:
© Copyright © 2020 Tulaeva, Kratzer, Campana, Curin, van Hage, Karsonova, Riabova, Karaulov, Khaitov, Pickl and Valenta.
PY - 2020/7/7
Y1 - 2020/7/7
N2 - Vaccines for infectious diseases have improved the life of the human species in a tremendous manner. The principle of vaccination is to establish de novo adaptive immune response consisting of antibody and T cell responses against pathogens which should defend the vaccinated person against future challenge with the culprit pathogen. The situation is completely different for immunoglobulin E (IgE)-associated allergy, an immunologically-mediated hypersensitivity which is already characterized by increased IgE antibody levels and T cell responses against per se innocuous antigens (i.e., allergens). Thus, allergic patients suffer from a deviated hyper-immunity against allergens leading to inflammation upon allergen contact. Paradoxically, vaccination with allergens, termed allergen-specific immunotherapy (AIT), induces a counter immune response based on the production of high levels of allergen-specific IgG antibodies and alterations of the adaptive cellular response, which reduce allergen-induced symptoms of allergic inflammation. AIT was even shown to prevent the progression of mild to severe forms of allergy. Consequently, AIT can be considered as a form of therapeutic vaccination. In this article we describe a strategy and possible road map for the use of an AIT approach for prophylactic vaccination against allergy which is based on new molecular allergy vaccines. This road map includes the use of AIT for secondary preventive vaccination to stop the progression of clinically silent allergic sensitization toward symptomatic allergy and ultimately the prevention of allergic sensitization by maternal vaccination and/or early primary preventive vaccination of children. Prophylactic allergy vaccination with molecular allergy vaccines may allow halting the allergy epidemics affecting almost 30% of the population as it has been achieved for vaccination against infectious diseases.
AB - Vaccines for infectious diseases have improved the life of the human species in a tremendous manner. The principle of vaccination is to establish de novo adaptive immune response consisting of antibody and T cell responses against pathogens which should defend the vaccinated person against future challenge with the culprit pathogen. The situation is completely different for immunoglobulin E (IgE)-associated allergy, an immunologically-mediated hypersensitivity which is already characterized by increased IgE antibody levels and T cell responses against per se innocuous antigens (i.e., allergens). Thus, allergic patients suffer from a deviated hyper-immunity against allergens leading to inflammation upon allergen contact. Paradoxically, vaccination with allergens, termed allergen-specific immunotherapy (AIT), induces a counter immune response based on the production of high levels of allergen-specific IgG antibodies and alterations of the adaptive cellular response, which reduce allergen-induced symptoms of allergic inflammation. AIT was even shown to prevent the progression of mild to severe forms of allergy. Consequently, AIT can be considered as a form of therapeutic vaccination. In this article we describe a strategy and possible road map for the use of an AIT approach for prophylactic vaccination against allergy which is based on new molecular allergy vaccines. This road map includes the use of AIT for secondary preventive vaccination to stop the progression of clinically silent allergic sensitization toward symptomatic allergy and ultimately the prevention of allergic sensitization by maternal vaccination and/or early primary preventive vaccination of children. Prophylactic allergy vaccination with molecular allergy vaccines may allow halting the allergy epidemics affecting almost 30% of the population as it has been achieved for vaccination against infectious diseases.
KW - Allergens/administration & dosage
KW - Animals
KW - Clinical Trials as Topic
KW - Desensitization, Immunologic
KW - Epitopes, B-Lymphocyte/immunology
KW - Epitopes, T-Lymphocyte/immunology
KW - Female
KW - Humans
KW - Hypersensitivity/prevention & control
KW - Immunoglobulin E/immunology
KW - Peptides/immunology
KW - Pregnancy
KW - Primary Prevention
KW - Secondary Prevention
KW - Treatment Outcome
KW - Vaccination/methods
KW - Vaccines/administration & dosage
KW - Vaccines, Virus-Like Particle/administration & dosage
UR - http://www.scopus.com/inward/record.url?scp=85088430249&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2020.01368
DO - 10.3389/fimmu.2020.01368
M3 - Review article
C2 - 32733455
SN - 1664-3224
VL - 11
SP - 1368
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1368
ER -