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Pru p 7 sensitization is a predominant cause of severe, cypress pollen-associated peach allergy.
Klingebiel, Caroline; Chantran, Yannick; Arif-Lusson, Rihane; Ehrenberg, Angelica E; Östling, Jonas; Poisson, Alain; Liabeuf, Valérie; Agabriel, Chantal; Birnbaum, Joëlle; Porri, Françoise; Sarrat, Anne; Apoil, Pol-André; Vivinus, Mylène; Garnier, Lorna; Chiriac, Anca Mirela; Caimmi, Davide-Paolo; Bourrain, Jean-Luc; Demoly, Pascal; Guez, Stéphane; Boralevi, Franck; Lovato, Bertrand; Palussière, Céline; Leroy, Sylvie; Bourrier, Thierry; Giovannini-Chami, Lisa; Gouitaa, Marion; Aferiat-Derome, Agnès; Charpin, Denis; Sofalvi, Tünde; Cabon-Boudard, Isabelle; Massabie-Bouchat, Yann-Patrick; Hofmann, Bernard; Bonardel, Nathalie; Dron-Gonzalvez, Mireille; Sterling, Benoît; Carsin, Ania; Vivinus, Serge; Poitevin, Bernard; Nicolau, Laureline; Liautard, Geneviève; Soler, Christophe; Mezouar, Soraya; Annesi-Maesano, Isabella; Mège, Jean-Louis; Lidholm, Jonas; Vitte, Joana.
Afiliação
  • Klingebiel C; Laboratoire Synlab Provence, Marseille, France.
  • Chantran Y; UPMC Univ Paris 06, INSERM UMRS 938, Centre de Recherche Saint-Antoine, team "Immune System, Neuroinflammation and Neurodegenerative Diseases", Hôpital Saint-Antoine, Sorbonne Universités, Paris, France.
  • Arif-Lusson R; Immunology Department, AP-HP Saint-Antoine Hospital, Paris, France.
  • Ehrenberg AE; Aix-Marseille Univ, IRD, APHM, MEPHI, IHU Méditerranée Infection, Marseille, France.
  • Östling J; Thermo Fisher Scientific, Uppsala, Sweden.
  • Poisson A; Thermo Fisher Scientific, Uppsala, Sweden.
  • Liabeuf V; Service de Pneumo-Allergologie, Hôpital Saint Joseph, Marseille, France.
  • Agabriel C; Aix-Marseille Univ, APHM, Hôpital Timone, Service de Dermatologie-Vénéréologie, Marseille, France.
  • Birnbaum J; Aix-Marseille Univ, APHM, Hôpital Timone, Service de Pédiatrie Multidisciplinaire, Marseille, France.
  • Porri F; Service de Pneumologie et Allergologie, CH du Pays d'Aix, Aix-en-Provence, France.
  • Sarrat A; Service de Pneumo-Allergologie, Hôpital Saint Joseph, Marseille, France.
  • Apoil PA; Laboratoire d'Immunologie et Immunogénétique, GH Pellegrin, CHU Bordeaux, Bordeaux, France.
  • Vivinus M; Institut Fédératif de Biologie, Hôpital Purpan, CHU Toulouse, Toulouse, France.
  • Garnier L; Laboratoire d'Immunologie, Hôpital de l'Archet, CHU Nice, Nice, France.
  • Chiriac AM; Laboratoire d'Immunologie, CH Lyon Sud, CHU Lyon, Pierre-Bénite, France.
  • Caimmi DP; Département de pneumologie et addictologie, CHU Montpellier, Hôpital Arnaud-de-Villeneuve, Univ Montpellier, Montpellier, France.
  • Bourrain JL; Sorbonne Universités, INSERM UMRS 1136, IPLESP, team EPAR, Paris, France.
  • Demoly P; Département de pneumologie et addictologie, CHU Montpellier, Hôpital Arnaud-de-Villeneuve, Univ Montpellier, Montpellier, France.
  • Guez S; Sorbonne Universités, INSERM UMRS 1136, IPLESP, team EPAR, Paris, France.
  • Boralevi F; Département de pneumologie et addictologie, CHU Montpellier, Hôpital Arnaud-de-Villeneuve, Univ Montpellier, Montpellier, France.
  • Lovato B; Département de pneumologie et addictologie, CHU Montpellier, Hôpital Arnaud-de-Villeneuve, Univ Montpellier, Montpellier, France.
  • Palussière C; Sorbonne Universités, INSERM UMRS 1136, IPLESP, team EPAR, Paris, France.
  • Leroy S; Unité d'allergologie, GH Pellegrin, CHU Bordeaux, Bordeaux, France.
  • Bourrier T; Unité de Dermatologie Pédiatrique, Hôpital Pellegrin-Enfants, CHU Bordeaux, Bordeaux, France.
  • Giovannini-Chami L; Medical Office, Mérignac, France.
  • Gouitaa M; Medical Office, Cenon, France.
  • Aferiat-Derome A; Service de Pneumologie, Hôpital Pasteur, CHU Nice, Nice, France.
  • Charpin D; Hôpitaux Pédiatriques de Nice, CHU Lenval, Nice, France.
  • Sofalvi T; Hôpitaux Pédiatriques de Nice, CHU Lenval, Nice, France.
  • Cabon-Boudard I; Aix-Marseille Univ, APHM, Hôpital Nord, Service de Pneumologie, Marseille, France.
  • Massabie-Bouchat YP; Medical Office, Les Jardins de Castellane, Marseille, France.
  • Hofmann B; Aix-Marseille Univ, APHM, Hôpital Timone, Unité de Pneumologie, Marseille, France.
  • Bonardel N; Aix-Marseille Univ, APHM, Hôpital Nord, Service de Pneumologie, Marseille, France.
  • Dron-Gonzalvez M; Aix-Marseille Univ, APHM, Hôpital Timone, Service de Chirurgie Pédiatrique, Marseille, France.
  • Sterling B; Medical Office, Marseille, France.
  • Carsin A; Medical Office, Carpentras, France.
  • Vivinus S; Médicale Victor Hugo, Avignon, France.
  • Poitevin B; Medical Office, Martigues, France.
  • Nicolau L; Medical Office, Marseille, France.
  • Liautard G; Aix-Marseille Univ, APHM, Hôpital Timone, Service de Pneumo-Pédiatrie, Marseille, France.
  • Soler C; Aix-Marseille Univ, APHM, Hôpital Timone, Service de Pneumo-Pédiatrie, Marseille, France.
  • Mezouar S; Service de Pneumologie, Hôpital Pasteur, CHU Nice, Nice, France.
  • Annesi-Maesano I; Medical Office, Bormes-les-Mimosas, France.
  • Mège JL; Medical Office, Perpignan, France.
  • Lidholm J; Medical Office, Solliès-Pont, France.
  • Vitte J; Laboratoire Synlab Provence, Marseille, France.
Clin Exp Allergy ; 49(4): 526-536, 2019 04.
Article em En | MEDLINE | ID: mdl-30672059
ABSTRACT

BACKGROUND:

Peach is a common elicitor of food allergic reactions. Peach-induced immediate reactions may occur as benign pollen-food syndromes, usually due to birch pollen-related PR-10 cross-reactivity in temperate climates, and as potentially severe primary food allergies, predominantly related to nsLTP Pru p 3 in Mediterranean regions. The newly described peach allergen Pru p 7 has gained recent attention as a potential peach allergy severity marker. Sensitization to Pru p 7 and its allergenic homologues of the gibberellin-regulated protein family occurs in areas with high Cupressaceae tree pollen exposure.

OBJECTIVE:

We sought to investigate the distribution, clinical characteristics and molecular associations of Pru p 7 sensitization among subjects with suspected peach allergy in different regions of France.

METHODS:

Subjects with suspected peach allergy (n = 316) were included. Diagnostic work-up was performed according to current guidelines, including open food challenge when required. IgE antibody measurements and competition experiments were performed using the ImmunoCAP assay platform.

RESULTS:

Sensitization to Pru p 7 was present in 171 (54%) of all subjects in the study and in 123 of 198 (62%) diagnosed as peach allergic, more than half of whom were sensitized to no other peach allergen. Frequency and magnitude of Pru p 7 sensitization were associated with the presence of peach allergy, the clinical severity of peach-induced allergic reactions and the level of cypress pollen exposure. Cypress pollen extract completely outcompeted IgE binding to Pru p 7. Pru p 7 was extremely potent in basophil activation tests. CONCLUSION AND CLINICAL RELEVANCE A subtype of Cupressaceae pollinosis, characterized by Pru p 7 sensitization, can be an underlying cause of severe peach allergy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pólen / Reações Cruzadas / Cupressus / Antígenos de Plantas / Prunus persica / Hipersensibilidade Alimentar Tipo de estudo: Etiology_studies / Guideline / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pólen / Reações Cruzadas / Cupressus / Antígenos de Plantas / Prunus persica / Hipersensibilidade Alimentar Tipo de estudo: Etiology_studies / Guideline / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article