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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Corylus

 
 
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Disease relevance of Corylus

  • In contrast, only four sera (22%) from 18 patients (group II) with tree pollen allergy but without any case history of nut hypersensitivity showed IgE binding to the 18 kd protein of hazelnut extract, and none of these sera exhibited IgE reactivity to the hazelnut profilin [1].
  • Binding of IgE from patients (with nut allergy) to the blotted hazelnut allergens could be blocked by preincubation of patients' sera with the recombinant proteins [1].
  • Patients with severe anaphylactic reactions to hazelnut showed specific IgE reactivity to a 9-kd allergen, totally inhibited by purified peach lipid-transfer protein (LTP), which was heat stable and, when purified, corresponded to an LTP [2].
  • CONCLUSIONS: Cor a 8 is a relevant allergen for a majority of Spanish patients with hazelnut allergy that can cause severe allergic reactions [3].
 

High impact information on Corylus

  • RESULTS: Pepsin completely destroyed IgE binding of all allergens within 1 second, and trypsin completely destroyed IgE binding of all allergens within 15 minutes, except for the major hazelnut allergen, which remained intact for 2 hours of trypsinolysis [4].
  • RESULTS: Mice fed hazelnut extract in combination with antiulcer drugs formed anaphylactogenic IgG1 toward hazelnut and developed type I skin reactivity to hazelnut extract [5].
  • METHODS: Extracted hazelnut proteins were separated by means of 2-dimensional PAGE, and immunolabeling was performed with individual sera from 14 patients with hazelnut-induced systemic reactions [6].
  • Sensitization to Bet v 1 was associated with IgE against apple, hazelnut, and peach, whereas sensitization to profilin was associated with positive RAST results to all investigated plant-derived foods except apple, peach, and melon [7].
  • RNAs were isolated from pollen of birch (Betula verrucosa), alder (Alnus glutinosa), hazel (Corylus avellana), and hornbeam (Carpinus betulus) [8].
 

Biological context of Corylus

 

Anatomical context of Corylus

  • OBJECTIVE: We compared the CD63-based basophil activation test (BAT) in the diagnosis of allergy to carrot, celery and hazelnut with skin prick tests (SPT) and measurement of allergen-specific IgE [13].
  • CONCLUSIONS: The major hazelnut allergen cross-reacts with the major allergens of birch and hazel pollen but apparently contains a relevant T cell epitope not shared with pollen allergens [14].
  • Lipase-catalyzed acidolysis of tripalmitin with hazelnut oil fatty acids and stearic acid to produce human milk fat substitutes [15].
  • Influence on hazelnut oil administration on peroxidation status of erythrocytes and apolipoprotein B 100-containing lipoproteins in rabbits fed on a high cholesterol diet [16].
 

Associations of Corylus with chemical compounds

  • Identification of an 11S globulin as a major hazelnut food allergen in hazelnut-induced systemic reactions [6].
  • We analysed the triacylglycerol, tocopherol and sterol composition of hazelnut oil, olive oil and their mixtures (90% olive oil with 10% hazelnut oil, 70% olive with 30% hazelnut oil and 50% olive oil with 50% hazelnut oil) [17].
  • This method was applied to separate sterol fractions of hazelnut and virgin olive oils, and our results were compared with those of TLC method [18].
  • In contrast, the histamine-release test with hazelnut, apple, and melon gave sensitivities of 0.87, 0.71, and 1.00, respectively [19].
  • After two oral provocations with hazelnuts the patients were randomized to receive either 10 mg of astemizole or placebo daily for 2 weeks in a double blind protocol followed by two oral provocations [20].
 

Gene context of Corylus

  • The type 2 cytokine analyses revealed that hazelnut sensitization results from activation of IL-4 and IL-5, thus providing a mechanistic basis for hazelnut-specific IgE response [21].
  • Several Cor a 1.04-specific TCL and TCC reacted with pollen allergens albeit less pronounced than with the hazelnut allergen [14].
  • Virulence assessment clearly indicated that the group A strains are very virulent, whereas the group B strains proved to be mildly virulent for hazelnut [22].
  • Birch pollinosis and atopy caused by apple, peach, and hazelnut; comparison of three extraction procedures with two apple strains [23].
  • In fact the level of accumulation of three tested snoRNAs, R1, U14 and U3, is much higher in female inflorescence than in leaves or pollen of hazelnut [24].
 

Analytical, diagnostic and therapeutic context of Corylus

  • Inhibition ELISA showed that pre-incubation of sera with almond, Brazil nut or hazelnut extracts resulted in a decrease in IgE binding to peanut extract, indicating allergenic cross-reactivity [25].
  • The control group was injected (i.p.) with distilled water, while the three remaining groups received injections of corn oil, hazelnut oil, or peanut oil for five weeks (in a dose of 0.4 ml/kg/day--minimum amount of oil in which vitamin E could be dissolved) [9].
  • Comparative studies on tree pollen allergens. XIV. Characterization of the birch (Betula verrucosa) and hazel (Corylus avellana) pollen extracts by horizontal 2-D SDS-PAGE combined with electrophoretic transfer and IgE immunoautoradiography [26].

References

  1. Identification of common allergenic structures in hazel pollen and hazelnuts: a possible explanation for sensitivity to hazelnuts in patients allergic to tree pollen. Hirschwehr, R., Valenta, R., Ebner, C., Ferreira, F., Sperr, W.R., Valent, P., Rohac, M., Rumpold, H., Scheiner, O., Kraft, D. J. Allergy Clin. Immunol. (1992) [Pubmed]
  2. Identification of hazelnut major allergens in sensitive patients with positive double-blind, placebo-controlled food challenge results. Pastorello, E.A., Vieths, S., Pravettoni, V., Farioli, L., Trambaioli, C., Fortunato, D., Lüttkopf, D., Calamari, M., Ansaloni, R., Scibilia, J., Ballmer-Weber, B.K., Poulsen, L.K., Wütrich, B., Hansen, K.S., Robino, A.M., Ortolani, C., Conti, A. J. Allergy Clin. Immunol. (2002) [Pubmed]
  3. Recombinant lipid transfer protein Cor a 8 from hazelnut: a new tool for in vitro diagnosis of potentially severe hazelnut allergy. Schocker, F., Lüttkopf, D., Scheurer, S., Petersen, A., Cisteró-Bahima, A., Enrique, E., San Miguel-Moncín, M., Akkerdaas, J., van Ree, R., Vieths, S., Becker, W.M. J. Allergy Clin. Immunol. (2004) [Pubmed]
  4. Gastrointestinal digestion of Bet v 1-homologous food allergens destroys their mediator-releasing, but not T cell-activating, capacity. Schimek, E.M., Zwölfer, B., Briza, P., Jahn-Schmid, B., Vogel, L., Vieths, S., Ebner, C., Bohle, B. J. Allergy Clin. Immunol. (2005) [Pubmed]
  5. Antiulcer drugs promote oral sensitization and hypersensitivity to hazelnut allergens in BALB/c mice and humans. Schöll, I., Untersmayr, E., Bakos, N., Roth-Walter, F., Gleiss, A., Boltz-Nitulescu, G., Scheiner, O., Jensen-Jarolim, E. Am. J. Clin. Nutr. (2005) [Pubmed]
  6. Identification of an 11S globulin as a major hazelnut food allergen in hazelnut-induced systemic reactions. Beyer, K., Grishina, G., Bardina, L., Grishin, A., Sampson, H.A. J. Allergy Clin. Immunol. (2002) [Pubmed]
  7. IgE to Bet v 1 and profilin: cross-reactivity patterns and clinical relevance. Wensing, M., Akkerdaas, J.H., van Leeuwen, W.A., Stapel, S.O., Bruijnzeel-Koomen, C.A., Aalberse, R.C., Bast, B.J., Knulst, A.C., van Ree, R. J. Allergy Clin. Immunol. (2002) [Pubmed]
  8. Homology of the major birch-pollen allergen, Bet v I, with the major pollen allergens of alder, hazel, and hornbeam at the nucleic acid level as determined by cross-hybridization. Valenta, R., Breiteneder, H., Petternburger, K., Breitenbach, M., Rumpold, H., Kraft, D., Scheiner, O. J. Allergy Clin. Immunol. (1991) [Pubmed]
  9. Vegetable oils used as vitamin E vehicle affect the electrical activity of the rat heart. Ozdemir, S., Ayaz, M., Tuncer, T., Ugur, M., Turan, B. Physiological research / Academia Scientiarum Bohemoslovaca. (2003) [Pubmed]
  10. Isolation and characterisation of phytase from dormant Corylus avellana seeds. Andriotis, V.M., Ross, J.D. Phytochemistry (2003) [Pubmed]
  11. Cloning of oleosin, a putative new hazelnut allergen, using a hazelnut cDNA library. Akkerdaas, J.H., Schocker, F., Vieths, S., Versteeg, S., Zuidmeer, L., Hefle, S.L., Aalberse, R.C., Richter, K., Ferreira, F., van Ree, R. Molecular nutrition & food research. (2006) [Pubmed]
  12. Standardization of food allergen extracts for skin prick test. Skamstrup Hansen, K., Bindslev-Jensen, C., Skov, P.S., Sparholt, S.H., Nordskov Hansen, G., Niemeijer, N.R., Malling, H.J., Poulsen, L.K. J. Chromatogr. B Biomed. Sci. Appl. (2001) [Pubmed]
  13. CD63 expression on basophils as a tool for the diagnosis of pollen-associated food allergy: sensitivity and specificity. Erdmann, S.M., Heussen, N., Moll-Slodowy, S., Merk, H.F., Sachs, B. Clin. Exp. Allergy (2003) [Pubmed]
  14. Characterization of the T cell response to the major hazelnut allergen, Cor a 1.04: evidence for a relevant T cell epitope not cross-reactive with homologous pollen allergens. Bohle, B., Radakovics, A., Lüttkopf, D., Jahn-Schmid, B., Vieths, S., Ebner, C. Clin. Exp. Allergy (2005) [Pubmed]
  15. Lipase-catalyzed acidolysis of tripalmitin with hazelnut oil fatty acids and stearic acid to produce human milk fat substitutes. Sahin, N., Akoh, C.C., Karaali, A. J. Agric. Food Chem. (2005) [Pubmed]
  16. Influence on hazelnut oil administration on peroxidation status of erythrocytes and apolipoprotein B 100-containing lipoproteins in rabbits fed on a high cholesterol diet. Balkan, J., Hatipoğlu, A., Aykaç-Toker, G., Uysal, M. J. Agric. Food Chem. (2003) [Pubmed]
  17. Analysis of olive and hazelnut oil mixtures by high-performance liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry of triacylglycerols and gas-liquid chromatography of non-saponifiable compounds (tocopherols and sterols). Parcerisa, J., Casals, I., Boatella, J., Codony, R., Rafecas, M. Journal of chromatography. A. (2000) [Pubmed]
  18. Novel solid-phase extraction method to separate 4-desmethyl-, 4-monomethyl-, and 4,4'-dimethylsterols in vegetable oils. Azadmard-Damirchi, S., Dutta, P.C. Journal of chromatography. A. (2006) [Pubmed]
  19. Diagnostic evaluation of grass- and birch-allergic patients with oral allergy syndrome. Anhoej, C., Backer, V., Nolte, H. Allergy (2001) [Pubmed]
  20. Oral allergy syndrome: the effect of astemizole. Bindslev-Jensen, C., Vibits, A., Stahl Skov, P., Weeke, B. Allergy (1991) [Pubmed]
  21. Hazelnut Allergy: evidence that hazelnut can directly elicit specific IgE antibody response via activating type 2 cytokines in mice. Birmingham, N., Gangur, V., Samineni, S., Navuluri, L., Kelly, C. Int. Arch. Allergy Immunol. (2005) [Pubmed]
  22. Bacteria associated with hazelnut (Corylus avellana L.) decline are of two groups: Pseudomonas avellanae and strains resembling P. syringae pv. syringae. Scortichini, M., Marchesi, U., Rossi, M.P., Di Prospero, P. Appl. Environ. Microbiol. (2002) [Pubmed]
  23. Birch pollinosis and atopy caused by apple, peach, and hazelnut; comparison of three extraction procedures with two apple strains. de Groot, H., de Jong, N.W., Vuijk, M.H., Gerth van Wijk, R. Allergy (1996) [Pubmed]
  24. Hyper-expression of small nucleolar RNAs (snoRNAs) in female inflorescences of hazelnut (Corylus avellana L.) supports rRNA aggregation in vitro. Massardo, D.R., Esposito, B., Veneziano, A., Wolf, K., Alifano, P., Del Giudice, L. Plant Cell Physiol. (2003) [Pubmed]
  25. Immunological analysis of allergenic cross-reactivity between peanut and tree nuts. de Leon, M.P., Glaspole, I.N., Drew, A.C., Rolland, J.M., O'Hehir, R.E., Suphioglu, C. Clin. Exp. Allergy (2003) [Pubmed]
  26. Comparative studies on tree pollen allergens. XIV. Characterization of the birch (Betula verrucosa) and hazel (Corylus avellana) pollen extracts by horizontal 2-D SDS-PAGE combined with electrophoretic transfer and IgE immunoautoradiography. Florvaag, E., Holen, E., Vik, H., Elsayed, S. Annals of allergy. (1988) [Pubmed]
 
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