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Tree-Pollen-Related Food Allergies: Birch Pollen and More

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Abstract

Purpose of the Review

This review explores the connection between sensitization to tree pollen and reactivity to plant-based foods in clinical settings. It investigates whether this relationship is “causal,” “concurrent,” or “random,” while examining the underlying molecular mechanisms.

Recent Findings

Three scenarios are discussed: (a) cross-reactivity between tree pollen and foods due to shared molecular components, resulting in IgE-mediated food reactions; (b) tree pollen reactivity arising from cross-reactive molecules in foods, potentially complicating diagnosis; and (c) independent recognition of molecular components in tree pollen and foods. The roles of allergens like pathogenesis-related-protein group 10 (PR-10) in Fagales trees and non-specific lipid transfer proteins (nsLTPs) in olive and plane trees are explored for their cross-reactivity and adverse reaction potential. The role of gibberellin-regulated proteins (GRPs) in the “Cypress/Peach syndrome” is also investigated.

Summary of Major Conclusion

The review emphasizes complex interactions between tree pollen reactivity and food allergies, highlighting the need for thorough molecular reactivity diagnostics and detailed medical histories to understand these intricate connections. It underscores cross-reactivity among homologous allergens, the significance of structural similarity in causing adverse reactions, and the influence of co-factors on clinical outcomes. Ultimately, the review provides insights into the intricate nature of tree-related reactivity, offering implications for clinical diagnosis and management.

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“References and Recommended Reading

Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance

  1. •• Dramburg S, Hilger C, Santos AF, de las Vecillas L, Aalberse RC, Acevedo N, et al. EAACI molecular allergology user’s guide 2.0. Pediatr Allergy Immunol. 2023;34:1–386. This is the updated “bible” of molecular allergology.

  2. Aalberse RC. Structural biology of allergens. J Allergy Clin Immunol. 2000;106:228–38.

    Article  CAS  PubMed  Google Scholar 

  3. Biedermann T, Winther L, Till SJ, Panzner P, Knulst A, Valovirta E. Birch pollen allergy in Europe. Allergy: European. J Allergy Clin Immunol. 2019;74:1237–48.

    Article  CAS  Google Scholar 

  4. Wallner M, Erler A, Hauser M, Klinglmayr E, Gadermaier G, Vogel L, et al. Immunologic characterization of isoforms of Car b 1 and Que a 1, the major hornbeam and oak pollen allergens. Allergy. 2009;64:452–60.

    Article  CAS  PubMed  Google Scholar 

  5. Klingebiel C, Chantran Y, Arif-Lusson R, Ehrenberg AE, Östling J, Poisson A, et al. Pru p 7 sensitization is a predominant cause of severe, cypress pollen-associated peach allergy. Clin Exp Allergy. 2019;49:526–36.

    Article  CAS  PubMed  Google Scholar 

  6. Siekierzynska A, Piasecka-Kwiatkowska D, Myszka A, Burzynska M, Sozanska B, Sozanski T. Apple allergy: Causes and factors influencing fruits allergenic properties–Review. Clin Transl. Allergy. 2021:11.

  7. Geroldinger-Simic M, Zelniker T, Aberer W, Ebner C, Egger C, Greiderer A, et al. Birch pollen-related food allergy: Clinical aspects and the role of allergen-specific IgE and IgG4 antibodies. J Allergy Clin Immunol. 2011;127:616–622.e1. https://doi.org/10.1016/j.jaci.2010.10.027.

    Article  CAS  PubMed  Google Scholar 

  8. • Asero R, Brusca I, Cecchi L, Pignatti P, Pravettoni V, Scala E, et al. Why lipid transfer protein allergy is not a pollen-food syndrome: Novel data and literature review. Eur Ann Allergy Clin Immunol. 2022;54:198–206. A study tackling the concept that LTP allergy follows pollen sensitization.

    Article  CAS  PubMed  Google Scholar 

  9. Scala E, Abeni D, Bd DP, Paganelli R, Locanto M, Giani M, et al. Ole e 1, Ole e 7, and Ole e 9: Identifying distinct clinical subsets of olive tree–allergic patients. J Allergy Clin Immunol. 137:629–631.e3. https://doi.org/10.1016/j.jaci.2015.07.009.

  10. Lauer I, Miguel-Moncin MS, Abel T, Foetisch K, Hartz C, Fortunato D, et al. Identification of a plane pollen lipid transfer protein (Pla a 3) and its immunological relation to the peach lipid-transfer protein, Pru p 3. Clin Exp Allergy. 2007;37:261–9.

    Article  CAS  PubMed  Google Scholar 

  11. Wangorsch A, Larsson H, Messmer M, García-Moral A, Lauer I, Wolfheimer S, et al. Molecular cloning of plane pollen allergen Pla a 3 and its utility as diagnostic marker for peach associated plane pollen allergy. Clin Exp Allergy. 2016;46:764–74.

    Article  CAS  PubMed  Google Scholar 

  12. Scala E, Cecchi L, Abeni D, Guerra EC, Pirrotta L, Localnto M, Giani M, Asero R. Pla a 2 and Pla a 3 reactivities identify plane tree-allergic patients with respiratory symptoms or food allergy. Allergy. 2017;72:671–4.

    Article  CAS  PubMed  Google Scholar 

  13. Hauser M, Asam C, Himly M, Palazzo P, Voltolini S, Montanari C, et al. Bet v 1-like pollen allergens of multiple Fagales species can sensitize atopic individuals. Clin Exp Allergy. 2011;41:1804–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Radauer C, Lackner P, Breiteneder H. The Bet v 1 fold: An ancient, versatile scaffold for binding of large, hydrophobic ligands. BMC Evol Biol. 2008;8:1–19.

    Article  Google Scholar 

  15. Ferreira FD, Hoffmann-Sommergruber K, Breiteneder H, Pettenburger K, Ebner C, Sommergruber W, et al. Purification and characterization of recombinant Bet v I, the major birch pollen allergen. Immunological equivalence to natural Bet v I. J Biol Chem. 1993;268:19574–80.

    Article  CAS  PubMed  Google Scholar 

  16. Breiteneder H, Pettenburger K, Bito A, Valenta R, Kraft D, Rumpold H, et al. The gene coding for the major birch pollen allergen BetvI, is highly homologous to a pea disease resistance response gene. EMBO J. 1989;8:1935–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Faber MA, Van Gasse AL, Decuyper II, Sabato V, Hagendorens MM, Mertens C, et al. Cross-reactive aeroallergens: Which need to cross our mind in food allergy diagnosis? Journal of Allergy and Clinical Immunology. In Pract. 2018;6:1813–23. https://doi.org/10.1016/j.jaip.2018.08.010.

    Article  Google Scholar 

  18. Pedrosa M, Guerrero-Sanchez VM, Canales-Bueno N, Loli-Ausejo D, Castillejo MÁ, Quirce S, et al. Quercus ilex pollen allergen, Que i 1, responsible for pollen food allergy syndrome caused by fruits in Spanish allergic patients. Clin Exp Allergy. 2020;50:815–23.

    Article  CAS  PubMed  Google Scholar 

  19. Kabasser S, Crvenjak N, Schmalz S, Kalic T, Hafner C, Dubiela P, et al. Pru du 1, the Bet v 1-homologue from almond, is a major allergen in patients with birch pollen associated almond allergy. Clin Transl Allergy. 2022;12:1–5.

    Article  Google Scholar 

  20. Scala E, Cecchi L, Guerra C. Molecular recognition profiles and clinical patterns of PR-10 sensitization in a birch-free Mediterranean area. Int Arch Allergy Immunol. 2017;173:138–46.

    Article  CAS  PubMed  Google Scholar 

  21. Breiteneder H, Ebner C. Molecular and biochemical classification of plant-derived food allergens. J Allergy Clin Immunol. 2000;106:27–36.

    Article  CAS  PubMed  Google Scholar 

  22. Rashid RS, Smith KA, Nambiar KZ, Frew AJ, Tarzi MD. Pollen-food syndrome is related to Bet v 1/PR-10 protein sensitisation, but not all patients have spring rhinitis. Allergy: European. J Allergy Clin Immunol. 2011;66:1391–2.

    Article  CAS  Google Scholar 

  23. Johnson PE, Van Der Plancken I, Balasa A, Husband FA, Grauwet T, Hendrickx M, et al. High pressure, thermal and pulsed electric-field-induced structural changes in selected food allergens. Mol Nutr Food Res. 2010;54:1701–10.

    Article  CAS  PubMed  Google Scholar 

  24. Mittag D, Vieths S, Vogel L, Becker WM, Rihs HP, Helbling A, et al. Soybean allergy in patients allergic to birch pollen: Clinical investigation and molecular characterization of allergens. J Allergy Clin Immunol. 2004;113:148–54.

    Article  CAS  PubMed  Google Scholar 

  25. Asero R, Celi GSE. Labile plant food allergens: Really so harmless? Case series and literature review. Allergy. 2020;75:1517–8.

    Article  PubMed  Google Scholar 

  26. Pühringer H, Moll D, Hoffmann-Sommergruber K, Watillon B, Katinger H, Da Câmara Machado ML. The promoter of an apple Ypr10 gene, encoding the major allergen Mal d 1, is stress- and pathogen-inducible. Plant Sci. 2000;152:35–50.

    Article  Google Scholar 

  27. Schmitz-Eiberger M, Matthes A. Effect of harvest maturity, duration of storage and shelf life of apples on the allergen Mal d 1, polyphenoloxidase activity and polyphenol content. Food Chem. 2011;127:1459–64. https://doi.org/10.1016/j.foodchem.2011.01.101.

    Article  CAS  Google Scholar 

  28. Sancho AI, Foxalll R, Browne T, Dey R, Zuidmeer L, Marzban G, et al. Effect of postharvest storage on the expression of the apple allergen Mal d 1. J Agric Food Chem. 2006;54:5917–23.

    Article  CAS  PubMed  Google Scholar 

  29. Cadot P, Díaz JF, Proost P, Van Damme J, Engelborghs Y, Stevens EAM, et al. Purification and characterization of an 18-kd allergen of birch (Betula verrucosa) pollen: Identification as a cyclophilin. J Allergy Clin Immunol. 2000;105:286–91.

    Article  CAS  PubMed  Google Scholar 

  30. Pazouki N, Sankian M, Leung PTY, Nejadsattari T, Khavari-Nejad RA, Varasteh AR. Identification of cyclophilin as a novel allergen from Platanus orientalis pollens by mass spectrometry. J Biosci Bioeng. 2009;107:215–7. https://doi.org/10.1016/j.jbiosc.2008.10.016.

    Article  CAS  PubMed  Google Scholar 

  31. Ghosh D, Mueller GA, Schramm G, Edwards LL, Petersen A, London RE, et al. Primary identification, biochemical characterization, and immunologic properties of the allergenic pollen cyclophilin Cat r 1. J Biol Chem. 2014;289:21374–85. https://doi.org/10.1074/jbc.M114.559971.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Fujita C, Moriyama T, Ogawa T. Identification of cyclophilin as an IgE-binding protein from carrots. Int Arch Allergy Immunol. 2001;125:44–50.

    Article  CAS  PubMed  Google Scholar 

  33. Mattsson L, Valcour A, Holmqvist M, Larsson H, Lidholm J. Cyclophilin – A novel cross-reactive determinant in peanut. Clin Exp Allergy. 2021;51:620–2.

    Article  PubMed  Google Scholar 

  34. Rodríguez R, Villalba M, Monsalve RI, Batanero E. The spectrum of olive pollen allergens. Int Arch Allergy Immunol. 2001;125:185–95.

    Article  PubMed  Google Scholar 

  35. García BE, Lizaso MT, Moreno C, Rodríguez R, Villalba MT, Ledesma A, et al. Oleaceae-induced pollinosis in an area with exposure to olive and ash trees. J Investig Allergol Clin Immunol. 2011;21:34–7.

    PubMed  Google Scholar 

  36. Khosravi GR, Assarehzadegan MA, Morakabati P, Akbari B, Dousti F. Cloning and expression of Aca f 1: A new allergen of Acacia farnesiana pollen. Cent Eur J Immunol. 2016;41:273–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Rodríguez R, Villalba M, Batanero E, Palomares O, Quiralte J, Salamanca G, et al. Olive pollen recombinant allergens: Value in diagnosis and immunotherapy. J Investig Allergol Clin Immunol. 2007;17:56–62.

    Google Scholar 

  38. Batanero E, Villalba M, Rodríouez R. Glycosylation site of the major allergen from olive tree pollen. Allergenic implications of the carbohydrate moiety. Mol Immunol. 1994;31:31–7.

    Article  CAS  PubMed  Google Scholar 

  39. Heer O, Bioscience V, Ree V. Assessment of the clinical relevance of plant-glycan specific IgE by in vivo challenge with transgenic human lactoferrin produced in rice. 2008;

    Google Scholar 

  40. Florido Lopez JF, Quiralte Enriquez J, De Saavedra Alías JMA, De San Pedro BS, Casañez EM. An allergen from Olea europaea pollen (Ole e 7) is associated with plant-derived food anaphylaxis. Allergy. 2002;57:53–9.

    Article  PubMed  Google Scholar 

  41. 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 

  42. Huecas S, Villalba M, Rodríguez R. Ole e 9, a major olive pollen allergen is a 1,3-β-glucanase: Isolation, characterization, amino acid sequence, and tissue specificity. J Biol Chem. 2001;276:27959–66.

    Article  CAS  PubMed  Google Scholar 

  43. Scala E, Abeni D, Guerra EC, Pirrotta L, Locanto M, Meneguzzi G, et al. β -1,3-glucanase rOle e 9 and MnSOD rAsp f 6 IgE reactivity are the signature of atopic dermatitis in the Mediterranean area. Clin Exp Allergy. 2020;50:487–98.

    Article  CAS  PubMed  Google Scholar 

  44. Barre A, Culerrier R, Granier C, Selman L, Peumans WJ, Van Damme EJM, et al. Mapping of IgE-binding epitopes on the major latex allergen Hev b 2 and the cross-reacting 1,3β-glucanase fruit allergens as a molecular basis for the latex-fruit syndrome. Mol Immunol. 2009;46:1595–604.

    Article  CAS  PubMed  Google Scholar 

  45. Ünsel M, Ardeniz Ö, Mete N, Ersoy R, Sin AZ, Gulbahar O, et al. Food allergy due to olive. J Investig Allergol Clin Immunol. 2009;19:497–9.

    PubMed  Google Scholar 

  46. Alcázar P, Cariñanos P, De Castro C, Guerra F, Moreno C, Domínguez-Vilches E, et al. Airborne plane-tree (Platanus hispanica) pollen distribution in the city of Córdoba, South-western Spain, and possible implications on pollen allergy. J Investig Allergol Clin Immunol. 2004;14:238–43.

    PubMed  Google Scholar 

  47. Nowak M, Szymanśka A, Grewling Ł. Allergic risk zones of plane tree pollen (Platanus sp.) in Poznan. Postepy Dermatol Alergol. 2012;29:156–60.

    Google Scholar 

  48. Pazouki N, Sankian M, Nejadsattari T, Khavari-Nejad RA, Varasteh AR. Oriental plane pollen allergy: Identification of allergens and cross-reactivity between relevant species. Allergy Asthma Proc. 2008;29:622–8.

    Article  PubMed  Google Scholar 

  49. Skypala IJ, Asero R, Barber D, Cecchi L, Diaz Perales A, Hoffmann-Sommergruber K, et al. Non-specific lipid-transfer proteins: Allergen structure and function, cross-reactivity, sensitization, and epidemiology. Clin Transl Allergy. 2021:11.

  50. Tordesillas L, Sirvent S, Díaz-Perales A, Villalba M, Cuesta-Herranz J, Rodríguez R, et al. Plant lipid transfer protein allergens: No cross-reactivity between those from foods and olive and Parietaria pollen. Int Arch Allergy Immunol. 2011;156:291–6.

    Article  CAS  PubMed  Google Scholar 

  51. Skypala IJ, Scala E, Cecchi L, Shamji MH, Till S. Lipid transfer protein allergy in the United Kingdom: Characterization and comparison with a matched Italian cohort 2019;1340–1351.

  52. Gao ZS, Yang ZW, Wu SD, Wang HY, Liu ML, Mao WL, et al. Peach allergy in China: A dominant role for mugwort pollen lipid transfer protein as a primary sensitizer. J Allergy Clin Immunol. 2013;131

  53. Kronfel CM, Cheng H, McBride JK, Nesbit JB, Krouse R, Burns P, et al. IgE epitopes of Ara h 9, Jug r 3, and Pru p 3 in peanut-allergic individuals from Spain and the US. Frontiers in Allergy. 2023;3:1–15.

    Article  Google Scholar 

  54. Skypala IJ, Bartra J, Ebo DG, Antje Faber M, Fernández-Rivas M, Gomez F, et al. The diagnosis and management of allergic reactions in patients sensitized to non-specific lipid transfer proteins. Allergy: European. J Allergy Clin Immunol. 2021.

  55. Pascal M, Vazquez-Ortiz M, Folque MM, Jimenez-Feijoo R, Lozano J, Dominguez O, et al. Asymptomatic LTP sensitisation is common in plant-food allergic children from the Northeast of Spain. Allergol Immunopathol (Madr). 2016;44:351–8. https://doi.org/10.1016/j.aller.2015.10.003.

    Article  CAS  PubMed  Google Scholar 

  56. Faber MA, Van Gasse AL, Decuyper II, Uyttebroek A, Sabato V, Hagendorens MM, et al. IgE-reactivity profiles to nonspecific lipid transfer proteins in a northwestern European country. J Allergy Clin Immunol. 2017;139:679–682.e5.

    Article  PubMed  Google Scholar 

  57. • Romano A, Gaeta F, Caruso C, Fiocchi A, Valluzzi RL. Evaluation and updated classification of acute hypersensitivity reactions to nonsteroidal anti-inflammatory drugs (NSAIDs): NSAID-exacerbated or -induced food allergy. J Allergy Clin Immunol Pract. 2023;11:1843–1853.e1. https://doi.org/10.1016/j.jaip.2023.03.036. A study highlighting the importance of NSAID in food allergy.

  58. Romano A, Scala E, Rumi G, Gaeta F, Caruso C, Alonzi C, et al. Lipid transfer proteins: The most frequent sensitizer in Italian subjects with food-dependent exercise-induced anaphylaxis. Clin Exp Allergy. 2012:1643–53.

  59. Cardona V, Luengo O, Garriga T, Izquierdo A. Co-factor-enhanced food allergy. Allergy. 2012;39:1316–8.

    Article  Google Scholar 

  60. Scala E, Till SJ, Asero R, Abeni D, Guerra EC, Pirrotta L, et al. Lipid transfer protein sensitization: Reactivity profiles and clinical risk assessment in an Italian cohort. Allergy: European. J Allergy Clin Immunol. 2015;70:933–43.

    Article  CAS  Google Scholar 

  61. Caimmi D, Barber D, Hoffmann-Sommergruber K, Amrane H, Bousquet PJ, Dhivert-Donnadieu H, et al. Understanding the molecular sensitization for cypress pollen and peach in the Languedoc-Roussillon area. Allergy: European. J Allergy Clin Immunol. 2013;68:249–51.

    Article  CAS  Google Scholar 

  62. Sánchez-López J, Asturias JA, Enrique E, Suárez-Cervera M, Bartra J. Cupressus arizonica pollen: A new pollen involved in the lipid transfer protein syndrome? J Investig Allergol Clin Immunol. 2011;21:522–6.

    PubMed  Google Scholar 

  63. Sénéchal H, Keykhosravi S, Couderc R, Selva MA, Shahali Y, Aizawa T, et al. Pollen/fruit syndrome: Clinical relevance of the cypress pollen allergenic gibberellin-regulated protein. Allergy Asthma Immunol Res. 2019;11:143–51.

    Article  PubMed  Google Scholar 

  64. Sénéchal H, Šantrůček J, Melčová M, Svoboda P, Zídková J, Charpin D, et al. A new allergen family involved in pollen food-associated syndrome: Snakin/gibberellin-regulated proteins. J Allergy Clin Immunol. 2018;141:411–414.e4.

    Article  PubMed  Google Scholar 

  65. Shahali Y, Nicaise P, Brazdva A, Charpin D, Scala E, Mari A, Sutra JP, Chollet-Martin S, H. Senechal PPoncet. Complementarity between microarray and immunoblot for the comparative evaluation of IgE repertoire of French and Italian cypress pollen allergic patients. Folia Biol (Praha). 2014;60:192–201.

    CAS  PubMed  Google Scholar 

  66. Tuppo L, Alessandri C, Pomponi D, Picone D, Tamburrini M, Ferrara R, et al. Peamaclein - A new peach allergenic protein: Similarities, differences and misleading features compared to Pru p 3. Clin Exp Allergy. 2013;43:128–40.

    Article  CAS  PubMed  Google Scholar 

  67. Tuppo L, Alessandri C, Pasquariello MS, Petriccione M, Giangrieco I, Tamburrini M, et al. Pomegranate cultivars: Identification of the new IgE-binding protein pommaclein and analysis of antioxidant variability. J Agric Food Chem. 2017;65:2702–10.

    Article  CAS  PubMed  Google Scholar 

  68. Inomata N, Miyakawa M, Aihara M. Gibberellin-regulated protein in Japanese apricot is anallergen cross-reactive to Pru p 7. Immun Inflamm Dis. 2017;5:569–79.

    Article  Google Scholar 

  69. Inomata N, Miyakawa M, Ikeda N, Oda K, Aihara M. Identification of gibberellin-regulated protein as a new allergen in orange allergy. Clin Exp Allergy. 2018;48:1509–20.

    Article  CAS  PubMed  Google Scholar 

  70. Inomata N. Gibberellin-regulated protein allergy: Clinical features and cross-reactivity. Allergol Int. 2020;69:11–8. https://doi.org/10.1016/j.alit.2019.10.007.

    Article  CAS  PubMed  Google Scholar 

  71. Tuppo L, Alessandri C, Giangrieco I, Ciancamerla M, Rafaiani C, Tamburrini M, et al. Isolation of cypress gibberellin-regulated protein: Analysis of its structural features and IgE binding competition with homologous allergens. Mol Immunol. 2019;114:189–95. https://doi.org/10.1016/j.molimm.2019.07.023.

    Article  CAS  PubMed  Google Scholar 

  72. • Asero R, Abbadessa S, Aruanno A, Barilaro G, Barzaghi C, Bignardi D, et al. Sensitization to gibberellin-regulated protein (peamaclein) among Italian cypress pollen–sensitized patients. J Investig Allergol Clin Immunol. 2022;32:40–7. A multicenter study investigating the relevance of gibberellin-regulated protein as a food allergen in Italy, that discovered other hitherto unknown cross-reacting allergens in pollen ad food.

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Enrico Scala, Alessandro Maria Marra, Valeria Villella, Giorgio Celi, and Riccardo Asero each declare no potential conflicts of interest.

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Scala, E., Marra, A.M., Villella, V. et al. Tree-Pollen-Related Food Allergies: Birch Pollen and More. Curr Treat Options Allergy 10, 401–412 (2023). https://doi.org/10.1007/s40521-023-00352-7

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