"Default'' versus "pre-atopic'' IgG responses to foodborne and airborne pathogenesis-related group 10 protein molecules in birch-sensitized and nonatopic children

被引:37
作者
Hofmaier, Stephanie [1 ]
Hatzler, Laura [1 ]
Rohrbach, Alexander [1 ]
Panetta, Valentina [2 ]
Hakimeh, Dani [1 ]
Bauer, Carl Peter [3 ]
Hoffman, Ute [3 ]
Forster, Johannes [4 ]
Zepp, Fred [5 ]
Schuster, Antje [6 ]
Stock, Philippe [1 ]
Wahn, Ulrich [1 ]
Keil, Thomas [7 ,8 ]
Lau, Susanne [1 ]
Matricardi, Paolo Maria [1 ]
机构
[1] Charite, Dept Paediat Pneumol & Immunol, D-13353 Berlin, Germany
[2] Laltrastat Srl, Consultancy & Training, Biostat Off, Rome, Italy
[3] Tech Univ Munich, Dept Pediat, D-80290 Munich, Germany
[4] St Josefs Hosp, Dept Pediat St Hedwig, Freiburg, Germany
[5] Johannes Gutenberg Univ Mainz, Ctr Med, Dept Pediat & Adolescent Med, D-55122 Mainz, Germany
[6] Univ Dusseldorf, Dept Pediat Cardiol & Pneumol, Dusseldorf, Germany
[7] Charite, Inst Social Med Epidemiol & Hlth Econ, D-13353 Berlin, Germany
[8] Univ Wurzburg, Inst Clin Epidemiol & Biometry, Wurzburg, Germany
关键词
Allergen; Bet v 1; birch pollen; birth cohort; childhood; IgE; IgG; pathogenesis-related group 10 protein; SUBCLASS ANTIBODIES; ALLERGY; FOOD; CAT; CHILDHOOD; EXPOSURE; AFFINITY; WHEAT; LIFE; DOG;
D O I
10.1016/j.jaci.2014.09.048
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The route and dose of exposure are believed to be relevant factors in the sensitization process. Pathogenesis-related group 10 protein (PR-10) molecules are a family of allergenic proteins shared by many pollens (eg, birch and alder) and foods (eg, apple, peach, and soy). Children are exposed to both pollen-derived (inhaled) and food-derived (ingested) PR-10 molecules. Objective: We sought to investigate the role of route and dose of exposure in the evolution of IgG and IgE responses to recombinant PR-10 molecules. Methods: The German Multicentre Allergy Study examined a birth cohort born in 1990. Blood samples were collected at the ages of 1, 2, 3, 5, 6, 7, 10, and 13 years. Participants were included in the present analysis if they had (1) at least 1 serum sample at each of the 4 age periods or time points (1-3 years, 5-7 years, 10 years, and 13 years) and (2) IgE responses to birch (children with birch atopy) or no IgE response at all to 9 common aeroallergens and food allergens (nonatopic children). Therefore serum IgE antibodies to a panel of 4 airborne and 5 foodborne extracts, as well as to Bet v 1, were measured in singleplex assays, whereas IgG and IgE antibodies to a panel of 3 airborne PR-10 molecules (rBet v 1, rAln g 1, and rCor a 1.0101) and 7 foodborne PR-10 molecules (rCor a 1.0401, rMal d 1, rPru p 1, rGly m 4, rAra h 8, rApi g 1, and rDau c 1) were tested by using a multiplex microarray. Results: In the present analyses we included 28 children with birch atopy and randomly selected 28 nonatopic children from the 190 children fulfilling the inclusion criteria. Two different patterns of IgG responses to PR-10 molecules were identified. Among nonatopic subjects, a 'default'' IgG response was directed mostly against foodborne PR-10, started often before age 2 years, stayed weak, and was mostly transient. Among all atopic subjects, the default IgG response at age 1 year was overwhelmed after age 2 years by an 'pre-atopic'' IgG response, which started with or shortly before the IgE response and was intense and persistent. This atopic IgG response, as well as the IgE response, involved progressively more foodborne PR-10 proteins with frequencies and levels related to their homology with Bet v 1. Conclusions: The results suggest that children have a default antibody response to PR-10 molecules, which is early, weak, and transient; does not involve IgE; and is initiated by foodborne PR-10. By contrast, an atopic antibody response to PR-10 molecules is delayed, strong, and persistent; involves both IgG and IgE; and is initiated by airborne PR-10.
引用
收藏
页码:1367 / U435
页数:16
相关论文
共 34 条
[21]   Wheezing in childhood:: incidence, longitudinal patterns and factors predicting persistence [J].
Matricardi, P. M. ;
Illi, S. ;
Grueber, C. ;
Keil, T. ;
Nickel, R. ;
Wahn, U. ;
Lau, S. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (03) :585-592
[22]   Primary versus secondary immunoglobulin E sensitization to soy and wheat in the Multi-Centre Allergy Study cohort [J].
Matricardi, P. M. ;
Bockelbrink, A. ;
Beyer, K. ;
Keilw, T. ;
Niggemann, B. ;
Grueber, C. ;
Wahn, U. ;
Lau, S. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2008, 38 (03) :493-500
[23]   The ImmunoCAP ISAC molecular allergology approach in adult multi-sensitized Italian patients with respiratory symptoms [J].
Melioli, Giovanni ;
Bonifazi, Floriano ;
Bonini, Sergio ;
Maggi, Enrico ;
Mussap, Michele ;
Passalacqua, Gianni ;
Rossi, Enzo Renato ;
Vacca, Angelo ;
Canonica, Giorgio Walter .
CLINICAL BIOCHEMISTRY, 2011, 44 (12) :1005-1011
[24]  
Niederberger V, 2002, EUR J IMMUNOL, V32, P576, DOI 10.1002/1521-4141(200202)32:2<576::AID-IMMU576>3.0.CO
[25]  
2-U
[26]   Serum IgG and IgG4 antibodies to Fel d 1 among children exposed to 20 μg Fel d 1 at home:: Relevance of a nonallergic modified Th2 response [J].
Platts-Mills, TAE ;
Vaughan, JW ;
Blumenthal, K ;
Squillace, SP ;
Sporik, RB .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2001, 124 (1-3) :126-129
[27]   Triggers of IgE class switching and allergy development [J].
Poulsen, Lars K. ;
Hummelshoj, Lone .
ANNALS OF MEDICINE, 2007, 39 (06) :440-456
[28]  
Richard C, 2012, EUR ANN ALLERGY CLIN, V44, P243
[29]   Differences in the intrinsic immunogenicity and allergenicity of Bet v 1 and related food allergens revealed by site-directed mutagenesis [J].
Roulias, A. ;
Pichler, U. ;
Hauser, M. ;
Himly, M. ;
Hofer, H. ;
Lackner, P. ;
Ebner, C. ;
Briza, P. ;
Bohle, B. ;
Egger, M. ;
Wallner, M. ;
Ferreira, F. .
ALLERGY, 2014, 69 (02) :208-215
[30]   DEVELOPMENT OF IGE AND IGG ANTIBODIES TO FOOD AND INHALANT ALLERGENS IN CHILDREN AT RISK OF ALLERGIC DISEASE [J].
ROWNTREE, S ;
COGSWELL, JJ ;
PLATTSMILLS, TAE ;
MITCHELL, EB .
ARCHIVES OF DISEASE IN CHILDHOOD, 1985, 60 (08) :727-735