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Food allergies resulting from immunological cross-reactivity with inhalant allergens

Guidelines from the German Society for Allergology and Clinical Immunology (DGAKI), the German Dermatology Society (DDG), the Association of German Allergologists (AeDA) and the Society for Pediatric Allergology and Environmental Medicine (GPA)

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Summary

A large proportion of immunoglobulin E (IgE)-mediated food allergies in older children, adolescents and adults are caused by cross-reactive allergenic structures. Primary sensitization is most commonly to inhalant allergens (e.g. Bet v 1, the major birch pollen allergen). IgE can be activated by various cross-reactive allergens and lead to a variety of clinical manifestations. In general, local and mild — in rare cases also severe and systemic — reactions occur directly after consumption of the food containing the cross-reactive allergen (e. g. plant-derived foods containing proteins of the Bet v 1 family). In clinical practice, sensitization to the primary responsible inhalant and/or food allergen can be detected by skin prick tests and/or in vitro detection of specific IgE. Component-based diagnostic methods can support clinical diagnosis. For individual allergens, these methods may be helpful to estimate the risk of systemic reactions. Confirmation of sensitization by oral provocation testing is important particulary in the case of unclear case history. New, as yet unrecognized allergens can also cause cross-reactions.

The therapeutic potential of specific immunotherapy (SIT) with inhalant allergens and their effect on pollen-associated food allergies is currently unclear: results vary and placebo-controlled trials will be necessary in the future. Pollen allergies are very common. Altogether allergic sensitization to pollen and cross-reactive food allergens are very common in our latitudes. The actual relevance has to be assessed on an individual basis using the clinical information.

Cite this as Worm M, Jappe U, Kleine-Tebbe J, Schäfer C, Reese I, Saloga J, Treudler R, Zuberbier T, Wassmann A, Fuchs T, Dölle S, Raithel M, Ballmer-Weber B, Niggemann B, Werfel T. Food allergies resulting from immunological cross-reactivity with inhalant allergens. Allergo J Int 2014; 23: 1–16 DOI 10.1007/s40629-014-0004-6

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Abbreviations

AD:

Atopic dermatitis

CCD:

Cross-reactive carbohydrate determinants

EAACI:

European Academy of Allergy and Clinical Immunology

FEV1:

Forced expiratory volume in one second

FVC:

Forced vital capacity

IgE:

Immunoglobulin E

IgG:

Immunoglobulin G

LFS:

Latex-fruit syndrome

LTP:

Lipid transfer protein

NSAID:

Nonsteroidal anti-inflammatory drug

PR-10:

Pathogenesis-related protein family 10

SCORAD:

Scoring atopic dermatitis

sIgE:

Specific immunoglobulin E

SIT:

Specific immunotherapy

TLP:

Thaumatin-like proteins (PR-5)

VCin:

Inspiratory vital capacity

Literatur

  1. Kumar R. Epidemiology and risk factors for the development of food allergy. Pediatr Ann 2008; 37: 552–558

    PubMed  Google Scholar 

  2. Lack G. Epidemiologic risks for food allergy. J Allergy Clin Immunol 2008; 121: 1331–1336

    CAS  PubMed  Google Scholar 

  3. Ferreira F, Hawranek T, Gruber P, Wopfner N, Mari A. Allergic cross-reactivity: from gene to the clinic. Allergy 2004; 59: 243–267

    CAS  PubMed  Google Scholar 

  4. Bonds RS, Midoro-Horiuti T, Goldblum R. A structural basis for food allergy: the role of cross-reactivity. Curr Opin Allergy Clin Immunol 2008; 8: 82–86

    CAS  PubMed  Google Scholar 

  5. Hofmann A, Burks AW. Pollen food syndrome: update on the allergens. Curr Allergy Asthma Rep 2008; 8(5): 413–417

    PubMed  Google Scholar 

  6. Jappe U, Petersen A, Raulf-Heimsoth M. Allergische Soforttypreaktionen und kreuzreaktive Kohlenhydratepitope. Allergo J 2013; 22: 25–32

    Google Scholar 

  7. Mari A, Ballmer-Weber BK, Vieths S. The oral allergy syndrome: improved diagnostic and treatment methods. Curr Opin Allergy Clin Immunol 2005; 5: 267–273

    PubMed  Google Scholar 

  8. Fernández-Rivas M, Bolhaar S, González-Mancebo E, Asero R, Leeuwen A van, Bohle B et al. Apple allergy across Europe: how allergen sensitization profiles determine the clinical expression of allergies to plant foods. J Allergy Clin Immunol 2006; 118: 481–488

    PubMed  Google Scholar 

  9. Ballmer-Weber BK. Lipid transfer protein as a potential panallergen? Allergy 2002; 57: 873–875

    CAS  PubMed  Google Scholar 

  10. Ortolani C, Ballmer-Weber BK, Hansen KS, Ispano M, Wüthrich B, Bindslev-Jensen C et al. Hazelnut allergy: a double-blind, placebo-controlled food challenge multicenter study. J Allergy Clin Immunol 2000; 105: 577–581

    CAS  PubMed  Google Scholar 

  11. Worm M, Edenharter G, Ruëff F, Scherer K, Pföhler C, Mahler V et al. Symptom profile and risk factors of anaphylaxis in Central Europe. Allergy 2012; 67: 691–698

    CAS  PubMed  Google Scholar 

  12. Hompes S, Köhli A, Nemat K, Scherer K, Lange L, Rueff F et al. Provoking allergens and treatment of anaphylaxis in children and adolescents — data from the anaphylaxis registry of German-speaking countries. Pediatr Allergy Immunol 2011; 22: 568–574

    PubMed  Google Scholar 

  13. Reekers R, Busche M, Wittmann M, Kapp A, Werfel T. Birch pollen-related foods trigger atopic dermatitis in patients with specific cutaneous T-cell responses to birch pollen antigens. J Allergy Clin Immunol 1999; 104: 466–472

    CAS  PubMed  Google Scholar 

  14. Breuer K, Wulf A, Constien A, Tetau D, Kapp A, Werfel T. Birch pollen-related food as a provocation factor of allergic symptoms in children with atopic eczema/dermatitis syndrome. Allergy 2004; 59: 988–994

    CAS  PubMed  Google Scholar 

  15. Kleine-Tebbe J, Vogel L, Crowell DN, Haustein U, Vieths S. Severe oral allergy syndrome and anaphylactic reactions caused by a Bet v 1-related PR-10 protein in soybean, SAM22. J Allergy Clin Immunol 2002; 110: 797–804

    CAS  PubMed  Google Scholar 

  16. Worm M, Hompes S, Fiedler E, Illner A, Zuberbier T, Vieths S. Impact of native, heat-processed and encapsulated hazelnuts on the allergic response in hazelnut-allergic patients. Clin Exp Allergy 2009; 39: 159–166

    CAS  PubMed  Google Scholar 

  17. Schiappoli M, Senna G, Dama A, Bonadonna P, Crivellaro M, Passalacqua G. Anaphylaxis due to carrot as ridde food allergen. Allergol Immunopathol (Madr) 2002; 30: 243–244

    CAS  Google Scholar 

  18. Gómez M, Curiel G, Mendez J, Rodriguez M, Moneo I. Hypersensitivity to carrot associated with specific IgE to grass and tree pollens. Allergy 1996; 51: 425–429

    PubMed  Google Scholar 

  19. Paógan K, Götz-Żbikowska M, Tykwińska M, Napiórkowska K, Bartuzi Z. Celery — cause of severe anaphylactic shock. Postepy Hig Med Dosw (Online) 2012; 66: 132–134

    Google Scholar 

  20. Niggemann B, Beyer K, Erdmann E, Fuchs T, Kleine-Tebbe J, Lepp U et al. Standardisierung von oralen Provokationstests bei Verdacht auf Nahrungsmittelallergie. Allergo J 2011; 20: 149–160

    Google Scholar 

  21. Henzgen M, Ballmer-Weber BK, Erdmann S, Fuchs T, Kleine-Tebbe J, Lepp U et al. Hauttestungen mit Nahrungsmittelallergenen. Allergologie 2008; 31: 274–280

    Google Scholar 

  22. Bolhaar STHP, Weg WE van de, Ree R van, Gonzalez-Mancebo E, Zuidmeer L, Bruijnzeel-Koomen CAFM et al. In vivo assessment with prick-to-prick testing and double-blind, placebo-controlled food challenge of allergenicity of apple cultivars. J Allergy Clin Immunol 2005; 116: 1080–1086

    PubMed  Google Scholar 

  23. Osterballe M, Hansen TK, Mortz CG, Bindslev-Jensen C. The clinical relevance of sensitization to pollen-related fruits and vegetables in unselected pollen-sensitized adults. Allergy 2005; 60: 218–225

    CAS  PubMed  Google Scholar 

  24. Asero R, Mistrello G, Roncarolo D, Amato S, Zanoni D, Barocci F et al. Detection of clinical markers of sensitization to profilin in patients allergic to plant-derived foods. J Allergy Clin Immunol 2003; 112: 427–432

    CAS  PubMed  Google Scholar 

  25. Dölle S, Lehmann K, Schwarz D, Weckwert W, Scheler C, George E et al. Allergenic activity of different tomato cultivars in tomato allergic subjects. Clin Exp Allergy 2011; 41: 1643–1652

    PubMed  Google Scholar 

  26. Ballmer-Weber BK, Vieths S, Lüttkopf D, Heuschmann P, Wüthrich B. Celery allergy confirmed by double-blind, placebo-controlled food challenge: a clinical study in 32 subjects with a history of adverse reactions to celery root. J Allergy Clin Immunol 2000; 106: 373–378

    CAS  PubMed  Google Scholar 

  27. Ballmer-Weber BK, Wüthrich B, Wangorsch A, Fötisch K, Altmann F, Vieths S. Carrot allergy: double-blinded, placebo-controlled food challenge and identification of allergens. J Allergy Clin Immunol 2001; 108: 301–307

    CAS  PubMed  Google Scholar 

  28. Jappe U. Diagnostic reagents for type I allergy — what criteria should be applied to validation? Arb Paul Ehrlich Inst Bundesinstitut Impfstoffe Biomed Arzneim Langen Hess 2009; 96: 135–145; discussion 145-6

    PubMed  Google Scholar 

  29. Bruijnzeel-Koomen C, Ortolani C, Aas K, Bindslev-Jensen C, Björkstén B, Moneret-Vautrin D et al. Adverse reactions to food. European Academy of Allergology and Clinical Immunology Subcommittee. Allergy 1995; 50: 623–635

    CAS  PubMed  Google Scholar 

  30. Asero R, Ballmer-Weber BK, Beyer K, Conti A, Dubakiene R, Fernandez-Rivas M et al. IgE-mediated food allergy diagnosis: current status and new perspectives. Mol Nutr Food Res 2007; 51: 135–147

    CAS  PubMed  Google Scholar 

  31. Fötisch K, Vieths S. N- and O-linked oligosaccharides of allergenic glycoproteins. Glycoconj J 2001; 18: 373–390

    PubMed  Google Scholar 

  32. Mari A. IgE to cross-reactive carbohydrate determinants: analysis of the distribution and appraisal of the in vivo and in vitro reactivity. Int Arch Allergy Immunol 2002; 129: 286–295

    CAS  PubMed  Google Scholar 

  33. Mari A, Ooievaar-de Heer P, Scala E, Giani M, Pirrotta L, Zuidmeer L et al. Evaluation by double-blind placebo-controlled oral challenge of the clinical relevance of IgE antibodies against plant glycans. Allergy 2008; 63: 891–896

    CAS  PubMed  Google Scholar 

  34. Lüttkopf D, Ballmer-Weber BK, Wüthrich B, Vieths S. Celery allergens in patients with positive double-blind placebo-controlled food challenge. J Allergy Clin Immunol 2000; 106: 390–399

    PubMed  Google Scholar 

  35. Anliker MD, Reindl J, Vieths S, Wüthrich B. Allergy caused by ingestion of persimmon (Diospyros kaki): detection of specific IgE and cross-reactivity to profilin and carbohydrate determinants. J Allergy Clin Immunol 2001; 107: 718–723

    CAS  PubMed  Google Scholar 

  36. Foetisch K, Westphal S, Lauer I, Retzek M, Altmann F, Kolarich D et al. Biological activity of IgE specific for cross-reactive carbohydrate determinants. J Allergy Clin Immunol 2003; 111: 889–896

    CAS  PubMed  Google Scholar 

  37. Stapel SO, Asero R, Ballmer-Weber BK, Knol EF, Strobel S, Vieths S et al; EAACI Task Force. Testing for IgG4 against foods is not recommended as a diagnostic tool: EAACI Task Force Report. Allergy 2008; 63: 793–796

    CAS  PubMed  Google Scholar 

  38. Kleine-Tebbe J, Reese I, Ballmer-Weber B, Beyer K, Erdmann S, Fuchs T et al. Keine Empfehlung für IgG- und IgG4-Bestimmungen gegen Nahrungsmittel. Allergo J 2009; 18: 267–273

    Google Scholar 

  39. Skamstrup Hansen K, Vieths S, Vestergaard H, Skov PS, Bindslev-Jensen C, Poulsen LK. Seasonal variation in food allergy to apple. J Chromatogr B Biomed Sci Appl 2001; 756: 19–32

    CAS  PubMed  Google Scholar 

  40. Bindslev-Jensen C, Ballmer-Weber BK, Bengtsson U, Blanco C, Ebner C, Hourihane J et al; European Academy of Allergology and Clinical Immunology. Standardization of food challenges in patients with immediate reactions to foods — position paper from the European Academy of Allergology and Clinical Immunology. Allergy 2004; 59: 690–697

    CAS  PubMed  Google Scholar 

  41. Wüthrich B, Straumann F. Pollen crossreactivity. Can we establish a link between the in vitro results and the clinical situation? Allergy 1997; 52: 1187–1192

    PubMed  Google Scholar 

  42. Niggemann B, Beyer K, Erdmann S, Fuchs T, Kleine-Tebbe J, Lepp U et al. Standardisierung von oralen Provokationstests bei Verdacht auf Nahrungsmittelallergie. Allergologie 2011; 34: 467–479

    Google Scholar 

  43. Ballmer-Weber BK, Hoffmann A, Wüthrich B, Lüttkopf D, Pompei C, Wangorsch A et al. Influence of food processing on the allergenicity of celery: DBPCFC with celery spice and cooked celery in patients with celery allergy. Allergy 2002; 57: 228–235

    CAS  PubMed  Google Scholar 

  44. Henzgen M, Vieths S, Reese I, Erdmann S, Fuchs T, Jäger L et al. Nahrungsmittelallergien durch immunologische Kreuzreaktionen. Allergo J 2005; 14: 48–59

    Google Scholar 

  45. Werfel T, Aberer W, Augustin M, Biedermann T, Fölster-Holst R, Friedrichs F et al. Neurodermitis S2-Leitlinie. J Dtsch Dermatol Ges 2009; 7: S1–46

    Google Scholar 

  46. Lepp U, Ballmer-Weber B, Beyer K, Erdmann S, Fuchs T, Henzgen M et al. Therapiemöglichkeiten bei der IgE-vermittelten Nahrungsmittelallergie. Allergo J 2010; 3: 187–195

    Google Scholar 

  47. Asero R. Effects of birch pollen-specific immunotherapy on apple allergy in birch pollen-hypersensitive patients. Clin Exp Allergy 1998; 28: 1368–1373

    CAS  PubMed  Google Scholar 

  48. Henzgen M, Rudeschko O, Schlenvoigt G, Herrman D, Franke E. Immunparameter der Apfelallergie unter Hyposensibilisierung mit Birkenpollen. Allergologie 1999; 22: 655–664

    Google Scholar 

  49. Bolhaar ST, Tiemessen MM, Zuidmeer L, Leeuwen A van, Hoffmann-Sommergruber K, Bruijnzeel-Koomen CA et al. Efficacy of birch-pollen immunotherapy on cross-reactive food allergy confirmed by skin tests and double-blind food challenges. Clin Exp Allergy 2004; 34: 761–769

    CAS  PubMed  Google Scholar 

  50. Bucher X, Pichler WJ, Dahinden CA, Helbling A. Effect of tree pollen specific, subcutaneous immunotherapy on the oral allergy syndrome to apple and hazelnut. Allergy 2004; 59: 1272–1276

    CAS  PubMed  Google Scholar 

  51. Mauro M, Russello M, Incorvaia C, Gazzola G, Frati F, Moingeon P et al. Birch-apple syndrome treated with birch pollen immunotherapy. Int Arch Allergy Immunol 2011; 156: 416–422

    PubMed  Google Scholar 

  52. Hansen KS, Khinchi MS, Skov PS, Bindslev-Jensen C, Poulsen LK, Malling HJ. Food allergy to apple and specific immunotherapy with birch pollen. Mol Nutr Food Res 2004; 48: 441–448

    CAS  PubMed  Google Scholar 

  53. Hoffen E van, Peeters KA, Neerven RJ van, Tas CW van der, Zuidmeer L, Ieperen-van Dijk AG van et al. Effect of birch pollen-specific immunotherapy on birch pollen-related hazelnut allergy. J Allergy Clin Immunol 2011; 127: 100–101, 101.e1–3

    PubMed  Google Scholar 

  54. Kleine-Tebbe J, Ackermann-Simon J, Hanf G. Die spezifische Immuntherapie (Hyposensibilisierung) mit Allergenen zwischen wissenschaftlichem Fortschritt und medizinischer Versorgungsrealität. Bundesgesundheitsbl Gesundheitsforsch Gesundheitsschutz 2012; 55: 343–350

    CAS  Google Scholar 

  55. Ballmer-Weber BK, Holzhauser T, Scibilia J, Mittag D, Zisa G, Ortolani C et al. Clinical characteristics of soybean allergy in Europe: a double-blind, placebo-controlled food challenge study. J Allergy Clin Immunol 2007; 119: 1489–1496

    PubMed  Google Scholar 

  56. Mittag D, Akkerdaas J, Ballmer-Weber BK, Vogel L, Wensing M, Becker W et al. Ara h 8, a Bet v 1-homologous allergen from peanut, is a major allergen in patients with combined birch pollen and peanut allergy. J Allergy Clin Immunol 2004; 114: 1410–1417

    CAS  PubMed  Google Scholar 

  57. Hansen KS, Ballmer-Weber BK, Lüttkopf D, Skov PS, Wüthrich B, Bindslev-Jensen C et al. Roasted hazelnuts — allergenic activity evaluated by double-blind, placebo-controlled food challenge. Allergy 2003; 58: 132–138

    PubMed  Google Scholar 

  58. Bohle B, Zwölfer B, Heratizadeh A, Jahn-Schmid B, Antonia YD, Alter M et al. Cooking birch pollen-related food: divergent consequences for IgE- and T cell-mediated reactivity in vitro and in vivo. J Allergy Clin Immunol 2006; 118: 242–249

    CAS  PubMed  Google Scholar 

  59. Breiteneder H, Mills C. Structural bioinformatic approaches to understand cross-reactivity. Mol Nutr Food Res 2006; 50: 628–632

    CAS  PubMed  Google Scholar 

  60. Breiteneder H. Protein families: implications for allergen nomenclature, standardisation and specific immunotherapy. Arb Paul Ehrlich Inst Bundesinstitut Impfstoffe Biomed Arzneim Langen Hess 2009; 96: 249–254

    PubMed  Google Scholar 

  61. Egger M, Mutschlechner S, Wopfner N, Gadermaier G, Briza P, Ferreira F. Pollen-food syndromes associated with weed pollinosis: an update from the molecular point of view. Allergy 2006; 61: 461–476

    CAS  PubMed  Google Scholar 

  62. Gruber P, Gadermaier G, Bauer R, Weiss R, Wagner S, Leonard R et al. Role of the polypeptide backbone and post-translational modifications in cross-reactivity of Art v 1, the major mugwort pollen allergen. Biol Chem 2009; 390: 445–451

    CAS  PubMed  Google Scholar 

  63. Oberhuber C, Ma Y, Wopfner N, Gadermaier G, Dedic A, Niggemann B et al. Prevalence of IgE-binding to Art v 1, Art v 4 and Amb a 1 in mugwort-allergic patients. Int Arch Allergy Immunol 2008; 145: 94–101

    CAS  PubMed  Google Scholar 

  64. Guilloux L, Morisset M, Codreanu F, Parisot L, Moneret-Vautrin DA. Peanut allergy diagnosis in the context of grass pollen sensitization for 125 patients: roles of peanut and cross-reactive carbohydrate determinants specific IgE. Int Arch Allergy Immunol 2009; 149: 91–97

    CAS  PubMed  Google Scholar 

  65. Andersson K, Lidholm J. Characteristics and immunobiology of grass pollen allergens. Int Arch Allergy Immunol 2003; 130: 87–107

    CAS  PubMed  Google Scholar 

  66. Constantin C, Quirce S, Poorafshar M, Touraev A, Niggemann B, Mari A et al. Micro-arrayed wheat seed and grass pollen allergens for component-resolved diagnosis. Allergy 2009; 64: 1030–1037

    CAS  PubMed  Google Scholar 

  67. Anderson LB Jr, Dreyfuss EM, Logan J, Johnstone DE, Glaser J. Melon and banana sensitivity coincident with ragweed pollinosis. J Allergy 1970; 45: 310–319

    PubMed  Google Scholar 

  68. Enberg RN, Leickly FE, McCullough J, Bailey J, Ownby DR. Watermelon and ragweed share allergens. J Allergy Clin Immunol 1987; 79: 867–875

    CAS  PubMed  Google Scholar 

  69. Rodriguez J, Crespo JF, Burks W, Rivas-Plata C, Fernandez-Anaya S, Vives R et al. Randomized, double-blind, crossover challenge study in 53 subjects reporting adverse reactions to melon (Cucumis melo). J Allergy Clin Immunol 2000; 106: 968–972

    CAS  PubMed  Google Scholar 

  70. Rodriguez-Perez R, Crespo JF, Rodríguez J, Salcedo G. Profilin is a relevant melon allergen susceptible to pepsin digestion in patients with oral allergy syndrome. J Allergy Clin Immunol 2003; 111: 634–639

    CAS  PubMed  Google Scholar 

  71. Asero R. Ragweed allergy in northern Italy: are patterns of sensitization changing? Eur Ann Allergy Clin Immunol 2012; 44: 157–159

    CAS  PubMed  Google Scholar 

  72. Miralles JC, Caravaca F, Guillén F, Lombardero M, Negro JM. Cross-reactivity between Platanus pollen and vegetables. Allergy 2002; 57: 146–149

    CAS  PubMed  Google Scholar 

  73. Enrique E, Cisteró-Bahíma A, Bartolomé B, Alonso R, San Miguel-Moncín MM, Bartra J et al. Platanus acerifolia pollinosis and food allergy. Allergy 2002; 57(4): 351–356

    CAS  PubMed  Google Scholar 

  74. Asturias JA, Ibarrola I, Amat P, Tella R, Malet A, Cisteró-Bahíma A et al. Purified allergens vs. complete extract in the diagnosis of plane tree pollen allergy. Clin Exp Allergy 2006; 36: 1505–1512

    CAS  PubMed  Google Scholar 

  75. Enrique E, Alonso R, Bartolomé B, San Miguel-Moncín M, Bartra J, Fernández-Parra B et al. IgE reactivity to profilin in Platanus acerifolia pollen-sensitized subjects with plant-derived food allergy. J Investig Allergol Clin Immunol 2004; 14: 335–342

    CAS  PubMed  Google Scholar 

  76. Fernández-Rivas M, González-Mancebo E, Rodríguez-Pérez R, Benito C, Sánchez-Monge R, Salcedo G et al. Clinically relevant peach allergy is related to peach lipid transfer protein, Pru p 3, in the Spanish population. J Allergy Clin Immunol 2003; 112: 789–795

    PubMed  Google Scholar 

  77. Raulf-Heimsoth M, Rihs HP. Latexallergene: Sensibilisierungsquellen und Einzelallergenprofile erkennen. Allergo J 2011; 20: 241–243

    Google Scholar 

  78. Raulf-Heimsoth M, Rihs HP, Rozynek P, Cremer R, Gaspar A, Pires G et al. Quantitative analysis of immunoglobulin E reactivity profiles in patients allergic or sensitized to natural rubber latex (Hevea brasiliensis). J Allergy Clin Immunol 2003; 112: 1002–1007

    Google Scholar 

  79. Rihs HP, Dumont B, Rozynek P, Lundberg M, Cremer R, Bruning T et al. Molecular cloning, purification, and IgE-binding of a recombinant class I chitinase from Hevea brasiliensis leaves (rHev b 11.0102). Allergy 2003; 58: 246–251

    CAS  PubMed  Google Scholar 

  80. O’Riordain G, Radauer C, Hoffmann-Sommergruber K, Adhami F, Peterbauer CK, Blanco C et al. Cloning and molecular characterization of the Hevea brasiliensis allergen Hev b 11, a class I chitinase. Clin Exp Allergy 2002; 32: 455–462

    PubMed  Google Scholar 

  81. Wagner S, Breiteneder H. Hevea brasiliensis latex allergens: current panel and clinical relevance. Int Arch Allergy Immunol 2005; 136: 90–97

    CAS  PubMed  Google Scholar 

  82. Mikkola JH, Alenius H, Kalkkinen N, Turjanmaa K, Palosuo T, Reunala T. Hevein-like protein domains as a possible cause for allergen cross-reactivity between latex and banana. J Allergy Clin Immunol 1998; 102: 1005–1012

    CAS  PubMed  Google Scholar 

  83. Ibero M, Castillo MJ, Pineda F. Allergy to cassava: a new allergenic food with cross-reactivity to latex. J Investig Allergol Clin Immunol 2007; 17: 409–412

    CAS  PubMed  Google Scholar 

  84. Yagami A, Nakazawa Y, Suzuki K, Matsunaga K. Curry spice allergy associated with pollen-food allergy syndrome and latex fruit-syndrome. J Dermatol 2009; 36: 45–49

    PubMed  Google Scholar 

  85. Brehler R, Theissen U, Mohr C, Luger T. “Latex-fruit syndrome”: frequency of cross-reacting IgE antibodies. Allergy 1997; 52: 404–410

    CAS  PubMed  Google Scholar 

  86. Kleine-Tebbe J, Ballmer-Weber BK, Beyer K, Erdmann S, Fuchs T, Henzgen M et al. In-vitro-Diagnostik und molekulare Grundlagen von IgE-vermittelten Nahrungsmittelallergien. Allergo J 2009; 18: 132–146

    Google Scholar 

  87. Focke M, Hemmer W, Wöhrl S, Götz M, Jarisch R. Cross-reactivity between Ficus benjamina latex and fig fruit in patients with clinical fig allergy. Clin Exp Allergy 2003; 33: 971–977

    CAS  PubMed  Google Scholar 

  88. Hemmer W, Focke M, Götz M, Jarisch R. Sensitization to Ficus benjamina: relationship to natural rubber latex allergy and identification of foods implicated in the Ficus-fruit syndrome. Clin Exp Allergy 2004; 34: 1251–1258

    CAS  PubMed  Google Scholar 

  89. Antico A, Zoccatelli G, Marcotulli C, Curioni A. Oral allergy syndrome to fig. Int Arch Allergy Immunol 2003; 131: 138–142

    CAS  PubMed  Google Scholar 

  90. Hemmer W, Focke M, Marzban G, Swoboda I, Jarisch R, Laimer M. Identification of Bet v 1-related allergens in fig and other Moraceae fruits. Clin Exp Allergy 2010; 40: 679–687

    CAS  PubMed  Google Scholar 

  91. Quiralte J, Palacios L, Rodríguez R, Cárdaba B, Arias de Saavedra JM, Villalba M et al. Modelling diseases: the allergens of Olea europaea pollen. J Investig Allergol Clin Immunol 2007; 17 (Suppl 1): 24–30

    PubMed  Google Scholar 

  92. Martínez A, Asturias JA, Monteseirín J, Moreno V, García-Cubillana A, Hernández M et al. The allergenic relevance of profilin (Ole e 2) from Olea europaea pollen. Allergy 2002; 57 (Suppl 71): 17–23

    PubMed  Google Scholar 

  93. Florido Lopez JF, Quiralte Enriquez J, Arias de Saavedra Alías JM, Saenz de San Pedro B, Martin Casañez E. An allergen from Olea europaea pollen (Ole e 7) is associated with plant-derived food anaphylaxis. Allergy 2002; 57 (Suppl 71): 53–59

    PubMed  Google Scholar 

  94. Huecas S, Villalba M, Rodriguez R. Ole e 9, a major olive pollen allergen, is a 1,3 beta glucanase. Isolation, characterization, amino acid sequence, and tissue specificity. J Biol Chem 2001; 276: 27959–27966

    CAS  PubMed  Google Scholar 

  95. Palomares O, Villalba M, Quiralte J, Rodriguez R. Allergenic contribution of the IgE-reactive domains of the 1,3-beta glucanase Ole e 9: diagnostic value in olive pollen allergy. Ann Allergy Asthma Immunol 2006; 97: 61–65

    CAS  PubMed  Google Scholar 

  96. Reese G, Ayuso R, Lehrer SB. Tropomyosin: an invertebrate pan-allergen. Int Arch Allergy Immunol 1999; 119: 247–258

    CAS  PubMed  Google Scholar 

  97. Taylor SL. Molluscan shellfish allergy. Adv Food Nutr Res 2008; 54: 139–177

    CAS  PubMed  Google Scholar 

  98. Ayuso R, Reese G, Leong-Kee S, Plante M, Lehrer SB. Molecular basis of arthropod cross-reactivity: IgE-binding cross-reactive epitopes of shrimp, house dust mite and cockroach tropomyosins. Int Arch Allergy Immunol 2002; 129: 38–48

    CAS  PubMed  Google Scholar 

  99. Sidenius KE, Hallas TE, Poulsen LK, Mosbech H. Allergen cross-reactivity between house-dust mites and other invertebrates. Allergy 2001; 56: 723–733

    CAS  PubMed  Google Scholar 

  100. Drouet M, Boutet S, Lauret MG, Chène J, Bonneau JC, Le Sellin J et al. [The pork-cat syndrome or crossed allergy between pork meat and cat epithelia (1)]. Allerg Immunol (Paris) 1994; 26: 166–168, 171-2

    CAS  Google Scholar 

  101. Szépfalusi Z, Ebner C, Pandjaitan R, Orlicek F, Scheiner O, Boltz-Nitulescu G et al. Egg yolk alpha-livetin (chicken serum albumin) is a cross-reactive allergen in the bird-egg syndrome. J Allergy Clin Immunol 1994; 93: 932–942

    PubMed  Google Scholar 

  102. Quirce S, Díez-Gómez ML, Eiras P, Cuevas M, Baz G, Losada E. Inhalant allergy to egg yolk and egg white proteins. Clin Exp Allergy 1998; 28: 478–485

    CAS  PubMed  Google Scholar 

  103. Mandallaz MM, Weck AL de, Dahinden CA. Bird-egg syndrome. Cross-reactivity between bird antigens and egg-yolk livetins in IgE-mediated hypersensitivity. Int Arch Allergy Appl Immunol 1988; 87: 143–150

    CAS  PubMed  Google Scholar 

  104. Toorenenbergen AW van, Huijskes-Heins MI, Gerth van Wijk R. Different pattern of IgE binding to chicken egg yolk between patients with inhalant allergy to birds and food-allergic children. Int Arch Allergy Immunol 1994; 104: 199–203

    PubMed  Google Scholar 

  105. Hoffmann DR, Guenther DM. Occupational allergy to avian proteins presenting as allergy to ingestion of egg yolk. J Allergy Clin Immunol 1988; 81: 484–487

    Google Scholar 

  106. Quirce S, Marañón F, Umpiérrez A, Heras M de las, Fernández-Caldas E, Sastre J. Chicken serum albumin (Gal d 5*) is a partially heat-labile inhalant and food allergen implicated in the bird-egg syndrome. Allergy 2001; 56: 754–762

    CAS  PubMed  Google Scholar 

  107. Villas F, Compes E, Fernández-Nieto M, Muñoz MP, Bartolome B, Heras M de las. Bird-egg syndrome caused by Agapornis species (lovebird). J Investig Allergol Clin Immunol 2009; 19: 71–72

    CAS  PubMed  Google Scholar 

  108. Cisteró-Bahíma A, Enrique E, San Miguel-Moncín MM, Alonso R, Bartra J, Fernández-Parra B et al. Meat allergy and cross-reactivity with hamster epithelium. Allergy 2003 Feb; 58: 161–162

    PubMed  Google Scholar 

  109. Drouet M, Sabbah A, Le Sellin J, Bonneau JC, Gay G, Dubois-Gosnet C. [Fatal anaphylaxis after eating wild boar meat in a patient with pork-cat syndrome]. Allerg Immunol (Paris) 2001; 33: 163–165

    CAS  Google Scholar 

  110. San-Juan S, Lezaun A, Caballero ML, Moneo I. Occupational allergy to raw beef due to cross-reactivity with dog epithelium. Allergy 2005; 60: 839–840

    CAS  PubMed  Google Scholar 

  111. Hilger C, Kohnen M, Grigioni F, Lehners C, Hentges F. Allergic cross-reactions between cat and pig serum albumin. Study at the protein and DNA levels. Allergy 1997; 52: 179–187

    CAS  PubMed  Google Scholar 

  112. Cabañas R, López-Serrano MC, Carreira J, Ventas P, Polo F, Caballero MT et al. Importance of albumin in cross-reactivity among cat, dog and horse allergens. J Investig Allergol Clin Immunol 2000; 10(2): 71–77

    PubMed  Google Scholar 

  113. Hemmer W, Mayer D, Jarisch R. Fleischallergie. Allergologie 2011; 34: 373–387

    Google Scholar 

  114. Kinaciyan T, Jahn-Schmid B, Radakovics A, Zwölfer B, Schreiber C, Francis JN et al. Successful sublingual immunotherapy with birch pollen has limited effects on concomitant food allergy to apple and the immune response to the Bet v 1 homolog Mal d 1. J Allergy Clin Immunol 2007; 119: 937–943

    CAS  PubMed  Google Scholar 

  115. Kleine-Tebbe J, Bufe A, Ebner C, Eigenmann P, Friedrichs F, Fuch T et al. Specific Immunotherapy (hyposensitization) for IgE-mediated allergic diseases. Allergologie 2012; 33:3–34

    Google Scholar 

  116. Díez-Gómez ML, Quirce S, Aragoneses E, Cuevas M. Asthma caused by Ficus benjamina latex: evidence of cross-reactivity with fig fruit and papain. Ann Allergy Asthma Immunol 1998; 80: 24–30

    PubMed  Google Scholar 

  117. Vieths S, Scheurer S, Ballmer-Weber B. Current understanding of cross-reactivity of food allergens and pollen. Ann N Y Acad Sci 2002; 964: 47–68

    CAS  PubMed  Google Scholar 

  118. Vanek-Krebitz M, Hoffmann-Sommergruber K, Laimer da Camara Machado M, Susani M, Ebner C, Kraft D et al. Cloning and sequencing of Mal d 1, the major allergen from apple (Malus domestica), and its immunological relationship to Bet v 1, the major birch pollen allergen. Biochem Biophys Res Commun 1995; 214: 538–551

    CAS  PubMed  Google Scholar 

  119. Breiteneder H, Ferreira F, Hoffmann-Sommergruber K, Ebner C, Breitenbach M, Rumpold H et al. Four recombinant isoforms of Cor a I, the major allergen of hazel pollen, show different IgE-binding properties. Eur J Biochem 1993; 212: 355–362

    CAS  PubMed  Google Scholar 

  120. Breiteneder H, Hoffmann-Sommergruber K, O’Riordain G, Susani M, Ahorn H, Ebner C et al. Molecular characterization of Api g 1, the major allergen of celery (Apium graveolens), and its immunological and structural relationships to a group of 17-kDa tree pollen allergens. Eur J Biochem 1995; 233: 484–489

    CAS  PubMed  Google Scholar 

  121. Hoffmann-Sommergruber K, O’Riordain G, Ahorn H, Ebner C, Laimer Da Camara Machado M, Pühringer H et al. Molecular characterization of Dau c 1, the Bet v 1 homologous protein from carrot and its cross-reactivity with Bet v 1 and Api g 1. Clin Exp Allergy 1999; 29: 840–847

    CAS  PubMed  Google Scholar 

  122. Scheurer S, Metzner K, Haustein D, Vieths S. Molecular cloning, expression and characterization of Pru a 1, the major cherry allergen. Mol Immunol 1997; 34: 619–629

    CAS  PubMed  Google Scholar 

  123. Karamloo F, Scheurer S, Wangorsch A, May S, Haustein D, Vieths S. Pyr c 1, the major allergen from pear (Pyrus communis), is a new member of the Bet v 1 allergen family. J Chromatogr B Biomed Sci Appl 2001; 756: 281–293

    CAS  PubMed  Google Scholar 

  124. Oberhuber C, Bulley SM, Ballmer-Weber BK, Bublin M, Gaier S, DeWitt AM et al. Characterization of Bet v 1-related allergens from kiwifruit relevant for patients with combined kiwifruit and birch pollen allergy. Mol Nutr Food Res 2008; 52: S230–240

    Google Scholar 

  125. Mittag D, Vieths S, Vogel L, Becker W, Rihs H, Helbling A et al. Soybean allergy in patients allergic to birch pollen: clinical investigation and molecular characterization of allergens. J Allergy Clin Immunol 2004; 113: 148–154

    CAS  PubMed  Google Scholar 

  126. Mittag D, Vieths S, Vogel L, Wagner-Loew D, Starke A, Hunziker P et al. Birch pollen-related food allergy to legumes: identification and characterization of the Bet v 1 homologue in mungbean (Vigna radiata), Vig r 1. Clin Exp Allergy 2005; 35: 1049–1055

    CAS  PubMed  Google Scholar 

  127. Wüthrich B, Dietschi R. [The celery-carrot-mugwort-condiment syndrome: skin test and RAST results]. Schweiz Med Wochenschr 1985; 115: 258–264

    PubMed  Google Scholar 

  128. Figueroa J, Blanco C, Dumpiérrez AG, Almeida L, Ortega N, Castillo R et al. Mustard allergy confirmed by double-blind placebo-controlled food challenges: clinical features and cross-reactivity with mugwort pollen and plant-derived foods. Allergy 2005; 60: 48–55

    CAS  PubMed  Google Scholar 

  129. Pastorello EA, Pravettoni V, Farioli L, Rivolta F, Conti A, Ispano M et al. Hypersensitivity to mugwort (Artemisia vulgaris) in patients with peach allergy is due to a common lipid transfer protein allergen and is often without clinical expression. J Allergy Clin Immunol 2002; 110: 310–317

    CAS  PubMed  Google Scholar 

  130. Mari A, Scala E, D’Ambrosio C, Breiteneder H, Wagner S. Latex allergy within a cohort of not-at-risk subjects with respiratory symptoms: prevalence of latex sensitization and assessment of diagnostic tools. Int Arch Allergy Immunol 2007; 143: 135–143

    CAS  PubMed  Google Scholar 

  131. Raulf-Heimsoth M, Rihs HP, Rozynek P, Cremer R, Gaspar A, Pires G et al. Quantitative analysis of immunoglobulin E reactivity profiles in patients allergic or sensitized to natural rubber latex (Hevea brasiliensis). Clin Exp Allergy 2007; 37: 1657–1667

    CAS  PubMed  Google Scholar 

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Correspondence to Margitta Worm.

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Level of development

S1

AWMF-guidelineregister-number

061/019

Finalised

August 27, 2013

Valid until

Oktober 31, 2018

Check

Oktober 30, 2016

ICD-10-numbers

T78.1, T78.0, L27.2, T78.2

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www.springermedizin.de/allergo-journal

Methodology of guideline development

Literature reviews and expert consensus (February 20, 2013)

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Prof. Dr. Margitta Worm

Cite this as Worm M, Jappe U, Kleine-Tebbe J, Schäfer C, Reese I, Saloga J, Treudler R, Zuberbier T, Wassmann A, Fuchs T, Dölle S, Raithel M, Ballmer-Weber B, Niggemann B, Werfel T. Food allergies resulting from immunological cross-reactivity with inhalant allergens. Allergo J Int 2014; 23: 1–16 DOI 10.1007/s40629-014-0004-6

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The authors state that there are no conflicts of interest.

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Worm, M., Jappe, U., Kleine-Tebbe, J. et al. Food allergies resulting from immunological cross-reactivity with inhalant allergens. Allergo J Int 23, 1–16 (2014). https://doi.org/10.1007/s40629-014-0004-6

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