CoChat
Sign Up
Cited by 122

The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.

A WAO—ARIA—GA2LEN Consensus Document on Molecular-Based Allergy Diagnosis (PAMD@): Update 2020

Ansotegui, Ignacio J., Melioli, Giovanni, Canonica, Giorgio Walter, Gómez, R. Maximiliano, Jensen-Jarolim, Erika, Ebisawa, Motohiro, Luengo, Olga, Caraballo, Luis, Passalacqua, Giovanni, Poulsen, Lars K., Savi, Eleonora, Zuberbier, Torsten, Villa, Elisa, Oppenheimer, John, Asero, Riccardo, Bernstein, Jonathan, Bousquet, Jean, Cardona, Victoria, Cox, Lindo, Demoly, Pascal, Ferreira, Fatima, Giavina Bianchi, Pedro, Gonzalez Diaz, Sandra, Jakob, Thilo, Kase Tanno, Luciana, Kleine-Tebbe, Jorg, Levin, Michael, Martin, Bryan, Matricardi, Paolo Maria, Monge Ortega, Olga Patricia, Morais Almeida, Mario, Nunes, Carlos, Ortega Martell, José Antonio, Pawankar, Ruby, Renz, Harald, Rosário Filho, Nelson, Rouadi, Philip, Ruiba, Alessia, Sampson, Hugh, Sánchez Borges, Mario, Scala, Enrico, Schmid-Grendelmeier, Peter, Senna, Gian-Enrico, Sisul, Juan Carlos, Tang, Mimi L.K., Valenta, Rudolf, van Hage, Marianne, Wong, Gary W.K., Yáñez, Anahí·2020·World Allergy Organization Journal
DOI 10.1016/j.waojou.2019.100091PMC PMC7062937
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.waojou.2019.100091

Cites

17 of 17 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig. 1 Relevant molecules involved in the identification of cat, dog and horse sensitization
Fig. 1 Relevant molecules involved in the identification of cat, dog and horse sensitizationCC BY-NC-ND · PubMed Central
Fig. 2 A practical algorithm emplying allergen molecules for the identification of sensitization to hymenoptera. HBV: Honey bee venom; VYJV = Yallow Jacket venoms; PDV: polisted dominulus venom; CCD: Cross-reactive Carbohydrate Determinants
Fig. 2 A practical algorithm emplying allergen molecules for the identification of sensitization to hymenoptera. HBV: Honey bee venom; VYJV = Yallow Jacket venoms; PDV: polisted dominulus venom; CCD: Cross-reactive Carbohydrate DeterminantsCC BY-NC-ND · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 17 references

Research works printed but not linked: 315

  1. Fiocchi, 2014, Setting the stage of innovations in allergy globally, World Allergy Organ J, 7, 5, 10.1186/1939-4551-7-5 · DOI
  2. Luengo, 2014, Component resolved diagnosis: when should it be used?, Clin Transl Allergy, 4, 28, 10.1186/2045-7022-4-28 · DOI
  3. Tallar, 2015, Component-resolved allergen testing: the new frontier, World J Transl Med, 4, 44, 10.5528/wjtm.v4.i2.44 · DOI
  4. Van Gasse, 2015, Molecular allergy diagnosis: status anno 2015, Clin Chim Acta, 444, 54, 10.1016/j.cca.2015.02.012 · DOI
  5. Maruyama, 2016, Measurement of specific IgE antibodies to Ses i 1 improves the diagnosis of sesame allergy, Clin Exp Allergy, 46, 163, 10.1111/cea.12626 · DOI
  6. Pomes, 2018, WHO/IUIS allergen nomenclature: providing a common language, Mol Immunol, 100, 3, 10.1016/j.molimm.2018.03.003 · DOI
  7. Letran, 2013, Measurement of IgE to pollen allergen components is helpful in selecting patients for immunotherapy, Ann Allergy Asthma Immunol, 111, 295, 10.1016/j.anai.2013.07.005 · DOI · Paper page
  8. Hamilton, 2015, Serological IgE analyses in the diagnostic algorithm for allergic disease, J Allergy Clin Immunol Pract, 3, 833, 10.1016/j.jaip.2015.08.016 · DOI
  9. Jakob, 2015, Molecular allergy diagnostics using multiplex assays: methodological and practical considerations for use in research and clinical routine: Part 21 of the Series Molecular Allergology, Allergo J Int, 24, 320, 10.1007/s40629-015-0087-8 · DOI
  10. Woodfolk, 2015, Allergens, sources, particles, and molecules: why do we make IgE responses?, Allergol Int, 64, 295, 10.1016/j.alit.2015.06.001 · DOI
  11. Valenta, 2018, Molecular aspects of allergens and allergy, Adv Immunol, 138, 195, 10.1016/bs.ai.2018.03.002 · DOI
  12. Schulke, 2018, Induction of interleukin-10 producing dendritic cells as a tool to suppress allergen-specific T helper 2 responses, Front Immunol, 9, 455, 10.3389/fimmu.2018.00455 · DOI
  13. Wang, 2013, The innate immune response in house dust mite-induced allergic inflammation, Allergy Asthma Immunol Res, 5, 68, 10.4168/aair.2013.5.2.68 · DOI
  14. Jacquet, 2013, Innate immune responses in house dust mite allergy, ISRN Allergy, 2013, 735031, 10.1155/2013/735031 · DOI
  15. Satitsuksanoa, 2016, The minor house dust mite allergen Der p 13 is a fatty acid-binding protein and an activator of a TLR2-mediated innate immune response, Allergy, 71, 1425, 10.1111/all.12899 · DOI
  16. Fan, 2016, Allergen-dependent differences in ILC2s frequencies in patients with allergic rhinitis, Allergy Asthma Immunol Res, 8, 216, 10.4168/aair.2016.8.3.216 · DOI
  17. Guo, 2015, Innate immunological function of TH2 cells in vivo, Nat Immunol, 16, 1051, 10.1038/ni.3244 · DOI
  18. Lambrecht, 2014, Allergens and the airway epithelium response: gateway to allergic sensitization, J Allergy Clin Immunol, 134, 499, 10.1016/j.jaci.2014.06.036 · DOI
  19. Osterlund, 2009, The non-proteolytic house dust mite allergen Der p 2 induce NF-kappaB and MAPK dependent activation of bronchial epithelial cells, Clin Exp Allergy, 39, 1199, 10.1111/j.1365-2222.2009.03284.x · DOI
  20. Chiou, 2009, Der p2 activates airway smooth muscle cells in a TLR2/MyD88-dependent manner to induce an inflammatory response, J Cell Physiol, 220, 311, 10.1002/jcp.21764 · DOI
  21. Ye, 2011, Dermatophagoides pteronyssinus 2 regulates nerve growth factor release to induce airway inflammation via a reactive oxygen species-dependent pathway, Am J Physiol Lung Cell Mol Physiol, 300, L216, 10.1152/ajplung.00165.2010 · DOI
  22. Yu, 2015, Cell-penetrating peptide derived from human eosinophil cationic protein inhibits mite allergen Der p 2 induced inflammasome activation, PLoS One, 10
  23. Yin, 2015, Der p2 internalization by epithelium synergistically augments toll-like receptor-mediated proinflammatory signaling, Allergy Asthma Immunol Res, 7, 393, 10.4168/aair.2015.7.4.393 · DOI
  24. Trompette, 2009, Allergenicity resulting from functional mimicry of a Toll-like receptor complex protein, Nature, 457, 585, 10.1038/nature07548 · DOI
  25. Wang, 2011, Non-proteolytic house dust mite allergen, Der p 2, upregulated expression of tight junction molecule claudin-2 associated with Akt/GSK-3beta/beta-catenin signaling pathway, J Cell Biochem, 112, 1544, 10.1002/jcb.23067 · DOI
  26. Resch, 2016, Molecular, structural and immunological characterization of Der p 18, a chitinase-like house dust mite allergen, PLoS One, 11, 10.1371/journal.pone.0160641 · DOI
  27. Mueller, 2010, The structure of the dust mite allergen Der p 7 reveals similarities to innate immune proteins, J Allergy Clin Immunol, 125, 909, 10.1016/j.jaci.2009.12.016 · DOI
  28. Pulsawat, 2019, The house dust mite allergen Der p 5 binds lipid ligands and stimulates airway epithelial cells through a TLR2-dependent pathway, Clin Exp Allergy, 49, 378, 10.1111/cea.13278 · DOI
  29. Chevigne, 2018, Emerging roles of the protease allergen Der p 1 in house dust mite-induced airway inflammation, J Allergy Clin Immunol, 142, 398, 10.1016/j.jaci.2018.05.027 · DOI
  30. Pascual, 2011, Epigenetic changes in B lymphocytes associated with house dust mite allergic asthma, Epigenetics, 6, 1131, 10.4161/epi.6.9.16061 · DOI
  31. Shang, 2013, Epigenetic alterations by DNA methylation in house dust mite-induced airway hyperresponsiveness, Am J Respir Cell Mol Biol, 49, 279, 10.1165/rcmb.2012-0403OC · DOI
  32. Cheng, 2014, Alterations of the lung methylome in allergic airway hyper-responsiveness, Environ Mol Mutagen, 55, 244, 10.1002/em.21851 · DOI
  33. Zhang, 2018, Diesel exhaust and house dust mite allergen lead to common changes in the airway methylome and hydroxymethylome, Environ Epigenet, 4, dvy020, 10.1093/eep/dvy020 · DOI
  34. Liu, 2014, Laboratorial characteristics of patients with diarrhoea suffering from egg white allergy, Allergol Immunopathol, 42, 180, 10.1016/j.aller.2013.04.001 · DOI
  35. Stapel, 2008, Testing for IgG4 against foods is not recommended as a diagnostic tool: EAACI Task Force Report, Allergy, 63, 793, 10.1111/j.1398-9995.2008.01705.x · DOI · Paper page
  36. Werfel, 2015, Position paper of the EAACI: food allergy due to immunological cross-reactions with common inhalant allergens, Allergy, 70, 1079, 10.1111/all.12666 · DOI · Paper page
  37. Antico, 2011, Food-specific IgG4 lack diagnostic value in adult patients with chronic urticaria and other suspected allergy skin symptoms, Int Arch Allergy Immunol, 155, 52, 10.1159/000318736 · DOI
  38. Lucas Moreno, 2014, Diarrhoea due to allergy to egg: is there a role for specific IgG?, Allergol Immunopathol, 42, 177, 10.1016/j.aller.2014.05.001 · DOI
  39. Santos, 2015, IgG4 inhibits peanut-induced basophil and mast cell activation in peanut-tolerant children sensitized to peanut major allergens, J Allergy Clin Immunol, 135, 1249, 10.1016/j.jaci.2015.01.012 · DOI
  40. Hofmaier, 2015, Default" versus "pre-atopic" IgG responses to foodborne and airborne pathogenesis-related group 10 protein molecules in birch-sensitized and nonatopic children, J Allergy Clin Immunol, 135, 1367, 10.1016/j.jaci.2014.09.048 · DOI
  41. Bianchini, 2019, IgG4 drives M2a macrophages to a regulatory M2b-like phenotype: potential implication in immune tolerance, Allergy, 74, 483, 10.1111/all.13635 · DOI
  42. Flores Kim, 2018, Diagnostic accuracy, risk assessment, and cost-effectiveness of component-resolved diagnostics for food allergy: a systematic review, Allergy, 73, 1609, 10.1111/all.13399 · DOI
  43. Cardona, 2016, Component-resolved diagnosis in anaphylaxis, Curr Opin Allergy Clin Immunol, 16, 244, 10.1097/ACI.0000000000000261 · DOI
  44. Frick, 2016, Predominant Api m 10 sensitization as risk factor for treatment failure in honey bee venom immunotherapy, J Allergy Clin Immunol, 138, 1663, 10.1016/j.jaci.2016.04.024 · DOI
  45. Saltabayeva, 2017, Greater real-life diagnostic efficacy of allergen molecule-based diagnosis for prescription of immunotherapy in an area with multiple pollen exposure, Int Arch Allergy Immunol, 173, 93, 10.1159/000477442 · DOI
  46. van Hage, 2017, ImmunoCAP assays: pros and cons in allergology, J Allergy Clin Immunol, 140, 974, 10.1016/j.jaci.2017.05.008 · DOI · Paper page
  47. Garib, 2019, Determination of IgE and IgG reactivity to more than 170 allergen molecules in paper-dried blood spots, J Allergy Clin Immunol, 143, 437, 10.1016/j.jaci.2018.08.047 · DOI
  48. Heffler, 2018, Extended IgE profile based on an allergen macroarray: a novel tool for precision medicine in allergy diagnosis, World Allergy Organ J, 11, 7, 10.1186/s40413-018-0186-3 · DOI
  49. Di Fraia, 2019, A new molecular multiplex IgE assay for the diagnosis of pollen allergy in Mediterranean countries: a validation study, Clin Exp Allergy, 49, 341, 10.1111/cea.13264 · DOI
  50. Melioli, 2011, The ImmunoCAP ISAC molecular allergology approach in adult multi-sensitized Italian patients with respiratory symptoms, Clin Biochem, 44, 1005, 10.1016/j.clinbiochem.2011.05.007 · DOI
  51. Passalacqua, 2015, AIT (allergen immunotherapy): a model for the "precision medicine, Clin Mol Allergy, 13, 24, 10.1186/s12948-015-0028-6 · DOI
  52. Riccio, 2016, Molecular diagnosis and precision medicine in allergy management, Clin Chem Lab Med, 54, 1705, 10.1515/cclm-2016-0007 · DOI
  53. Kleine-Tebbe, 2016, Allergy work-up including component-resolved diagnosis: how to make allergen-specific immunotherapy more specific, Immunol Allergy Clin N AM, 36, 191, 10.1016/j.iac.2015.08.012 · DOI
  54. Martinez-Aranguren, 2014, Is the determination of specific IgE against components using ISAC 112 a reproducible technique?, PLoS One, 9, 10.1371/journal.pone.0088394 · DOI
  55. Lambert, 2015, The importance of EN ISO 15189 accreditation of allergen-specific IgE determination for reliable in vitro allergy diagnosis, Allergy, 70, 180, 10.1111/all.12546 · DOI
  56. Huss-Marp, 2015, Comparison of molecular and extract-based allergy diagnostics with multiplex and singleplex analysis, Allergo J Int, 24, 46, 10.1007/s40629-015-0046-4 · DOI
  57. Villalta, 2013, Isolated IgE reactivity to native walnut vicilin-like protein (nJug r 2) on ISAC microarray is due to cross-reactive carbohydrate epitopes, Clin Chem Lab Med, 51, 1991, 10.1515/cclm-2013-0027 · DOI
  58. Leonardi, 2015, Microarray-based IgE detection in tears of patients with vernal keratoconjunctivitis, Pediatr Allergy Immunol, 26, 641, 10.1111/pai.12450 · DOI
  59. Hochwallner, 2014, Transmission of allergen-specific IgG and IgE from maternal blood into breast milk visualized with microarray technology, J Allergy Clin Immunol, 134, 1213, 10.1016/j.jaci.2014.08.041 · DOI
  60. D'Amelio, 2016, Is the performance of ImmunoCAP ISAC 112 sufficient to diagnose peach and apple allergies?, Ann Allergy Asthma Immunol, 116, 162, 10.1016/j.anai.2015.11.003 · DOI
  61. Goikoetxea, 2016, Is microarray analysis really useful and sufficient to diagnose nut allergy in the mediterranean area?, J Investig Allergol Clin Immunol, 26, 31, 10.18176/jiaci.0005 · DOI
  62. Javaloyes, 2012, Pru p 3 acts as a strong sensitizer for peanut allergy in Spain, J Allergy Clin Immunol, 130, 1432, 10.1016/j.jaci.2012.08.038 · DOI
  63. Lupinek, 2014, Advances in allergen-microarray technology for diagnosis and monitoring of allergy: the MeDALL allergen-chip, Methods, 66, 106, 10.1016/j.ymeth.2013.10.008 · DOI
  64. Skrindo, 2015, The use of the MeDALL-chip to assess IgE sensitization: a new diagnostic tool for allergic disease?, Pediatr Allergy Immunol, 26, 239, 10.1111/pai.12366 · DOI
  65. Williams, 2016, Evaluation of a novel automated allergy microarray platform compared with three other allergy test methods, Clin Exp Immunol, 184, 1, 10.1111/cei.12721 · DOI
  66. Buzzulini, 2019, Evaluation of a new multiplex assay for allergy diagnosis, Clin Chim Acta, 493, 73, 10.1016/j.cca.2019.02.025 · DOI
  67. Matricardi, 2016, EAACI molecular allergology user's guide, Pediatr Allergy Immunol, 27, 1, 10.1111/pai.12563 · DOI · Paper page
  68. Canonica, 2018, Asthma: personalized and precision medicine, Curr Opin Allergy Clin Immunol, 18, 51, 10.1097/ACI.0000000000000416 · DOI
  69. Melioli, 2014, Allergenius, an expert system for the interpretation of allergen microarray results, World Allergy Organ J, 7, 15, 10.1186/1939-4551-7-15 · DOI
  70. Kuhne, 2015, A novel multipeptide microarray for the specific and sensitive mapping of linear IgE-binding epitopes of food allergens, Int Arch Allergy Immunol, 166, 213, 10.1159/000381344 · DOI
  71. Savilahti, 2014, Use of IgE and IgG4 epitope binding to predict the outcome of oral immunotherapy in cow's milk allergy, Pediatr Allergy Immunol, 25, 227, 10.1111/pai.12186 · DOI
  72. Lisson, 2016, Mapping of epitopes occurring in bovine alpha(s1)-Casein variants by peptide microarray immunoassay, Methods Mol Biol, 1352, 279, 10.1007/978-1-4939-3037-1_21 · DOI
  73. De-Simone, 2016, Spot synthesis: an optimized microarray to detect IgE epitopes, Methods Mol Biol, 1352, 263, 10.1007/978-1-4939-3037-1_20 · DOI
  74. Perez-Gordo, 2013, Epitope mapping of the major allergen from Atlantic cod in Spanish population reveals different IgE-binding patterns, Mol Nutr Food Res, 57, 1283, 10.1002/mnfr.201200332 · DOI
  75. Martinez-Botas, 2013, Mapping of the IgE and IgG4 sequential epitopes of ovomucoid with a peptide microarray immunoassay, Int Arch Allergy Immunol, 161, 11, 10.1159/000343040 · DOI · Paper page
  76. Gimenez, 2016, IgE epitope mapping using peptide microarray immunoassay, Methods Mol Biol, 1352, 251, 10.1007/978-1-4939-3037-1_19 · DOI
  77. Mehr, 2019, Innate immune activation occurs in acute food protein-induced enterocolitis syndrome reactions, J Allergy Clin Immunol, 144, 600, 10.1016/j.jaci.2019.04.021 · DOI
  78. Nowak-Wegrzyn, 2019, Food protein-induced enterocolitis syndrome in the US population-based study, J Allergy Clin Immunol, 144, 1128, 10.1016/j.jaci.2019.06.032 · DOI
  79. Feuille, 2019, Recognizing and Treating Food Protein-Induced Enterocolitis Syndrome, Allergy, 74, 2019, 10.1111/all.13857 · DOI
  80. Fedenko, 2016, Microarray-based IgE serology improves management of severe atopic dermatitis in two children, Pediatr Allergy Immunol, 27, 645, 10.1111/pai.12572 · DOI
  81. Posa, 2017, Evolution and predictive value of IgE responses toward a comprehensive panel of house dust mite allergens during the first 2 decades of life, J Allergy Clin Immunol, 139, 541, 10.1016/j.jaci.2016.08.014 · DOI · Paper page
  82. Wickman, 2017, Detection of IgE reactivity to a handful of allergen molecules in early childhood predicts respiratory allergy in adolescence, EBioMedicine, 26, 91, 10.1016/j.ebiom.2017.11.009 · DOI
  83. Passalacqua, 2013, The additional values of microarray allergen assay in the management of polysensitized patients with respiratory allergy, Allergy, 68, 1029, 10.1111/all.12194 · DOI
  84. Popescu, 2015, Cross-reactivity between aeroallergens and food allergens, World J Methodol, 5, 31, 10.5662/wjm.v5.i2.31 · DOI · Paper page
  85. Valenta, 2015, Food allergies: the basics, Gastroenterology, 148, 1120, 10.1053/j.gastro.2015.02.006 · DOI · Paper page
  86. Fotisch, 2001, N- and O-linked oligosaccharides of allergenic glycoproteins, Glycoconj J, 18, 373, 10.1023/A:1014860030380 · DOI · Paper page
  87. Berneder, 2013, Allergen chip diagnosis for soy-allergic patients: Gly m 4 as a marker for severe food-allergic reactions to soy, Int Arch Allergy Immunol, 161, 229, 10.1159/000345970 · DOI
  88. Roseler, 2013, [Anaphylaxis to PR-10 proteins (Bet v1 homologues)], Hautarzt, 64, 890, 10.1007/s00105-013-2683-1 · DOI
  89. Alvarado, 2014, Profilin as a severe food allergen in allergic patients overexposed to grass pollen, Allergy, 69, 1610, 10.1111/all.12509 · DOI · Paper page
  90. Uasuf, 2015, Different co-sensitizations could determine different risk assessment in peach allergy? Evaluation of an anaphylactic biomarker in Pru p 3 positive patients, Clin Mol Allergy, 13, 30, 10.1186/s12948-015-0035-7 · DOI
  91. Pastorello, 2011, Pru p 3-sensitised Italian peach-allergic patients are less likely to develop severe symptoms when also presenting IgE antibodies to Pru p 1 and Pru p 4, Int Arch Allergy Immunol, 156, 362, 10.1159/000324440 · DOI
  92. Van Hoeyveld, 2014, Diagnosis of food allergy Part 2. The use of allergen components for in vitro diagnosis of food allergy in children, Tijdschrift van de Belgische Kinderarts, 16, 112
  93. Borres, 2016, Recent advances in component resolved diagnosis in food allergy, Allergol Int, 65, 378, 10.1016/j.alit.2016.07.002 · DOI
  94. Ando, 2008, Utility of ovomucoid-specific IgE concentrations in predicting symptomatic egg allergy, J Allergy Clin Immunol, 122, 583, 10.1016/j.jaci.2008.06.016 · DOI
  95. Ohtani, 2016, Natural history of immediate-type hen's egg allergy in Japanese children, Allergol Int, 65, 153, 10.1016/j.alit.2015.10.005 · DOI
  96. Chokshi, 2015, Molecular diagnosis of egg allergy: an update, Expert Rev Mol Diagn, 15, 895, 10.1586/14737159.2015.1041927 · DOI
  97. Pattanaik, 2018, The changing face of anaphylaxis in adults and adolescents, Ann Allergy Asthma Immunol, 121, 594, 10.1016/j.anai.2018.07.017 · DOI
  98. Heaps, 2014, The utility of the ISAC allergen array in the investigation of idiopathic anaphylaxis, Clin Exp Immunol, 177, 483, 10.1111/cei.12334 · DOI
  99. Jappe, 2017, Relevance of lipophilic allergens in food allergy diagnosis, Curr Allergy Asthma Rep, 17, 61, 10.1007/s11882-017-0731-0 · DOI
  100. Matsuo, 2008, Sensitivity and specificity of recombinant omega-5 gliadin-specific IgE measurement for the diagnosis of wheat-dependent exercise-induced anaphylaxis, Allergy, 63, 233, 10.1111/j.1398-9995.2007.01504.x · DOI
  101. Pastorello, 2014, Wheat-dependent exercise-induced anaphylaxis caused by a lipid transfer protein and not by omega-5 gliadin, Ann Allergy Asthma Immunol, 112, 386, 10.1016/j.anai.2014.01.012 · DOI
  102. Cardona, 2012, Co-factor-enhanced food allergy, Allergy, 67, 1316, 10.1111/j.1398-9995.2012.02877.x. · DOI
  103. Romano, 2012, Lipid transfer proteins: the most frequent sensitizer in Italian subjects with food-dependent exercise-induced anaphylaxis, Clin Exp Allergy, 42, 1643, 10.1111/cea.12011 · DOI
  104. Apostolovic, 2020, Allergenomics of the tick Ixodes ricinus reveals important alpha-Gal-carrying IgE-binding proteins in red meat allergy, Allergy, 75, 217, 10.1111/all.13978 · DOI
  105. Levin, 2019, Galactose alpha-1,3-galactose phenotypes: lessons from various patient populations, Ann Allergy Asthma Immunol, 122, 598, 10.1016/j.anai.2019.03.021 · DOI · Paper page
  106. Wilson, 2018, Meat allergy and allergens, Mol Immunol, 100, 107, 10.1016/j.molimm.2018.03.018 · DOI
  107. Karaulov, 2018, Protein biomarkers in asthma, Int Arch Allergy Immunol, 175, 189, 10.1159/000486856 · DOI
  108. Jung, 2015, Comparison of component-resolved diagnosis by using allergen microarray with the conventional tests in allergic rhinitis patients: the first using in korea, Clin Exp Otorhinolaryngol, 8, 385, 10.3342/ceo.2015.8.4.385 · DOI
  109. Santosa, 2015, Evaluation of the applicability of the Immuno-solid-phase allergen chip (ISAC) assay in atopic patients in Singapore, Clin Transl Allergy, 5, 9, 10.1186/s13601-015-0053-z · DOI
  110. San Nicolo, 2016, Clinical relevance of IgE to profilin and/or polcalcin in pollen-sensitized patients, Int Arch Allergy Immunol, 169, 101, 10.1159/000444279 · DOI
  111. Jakob, 2017, Diagnostics in Hymenoptera venom allergy: current concepts and developments with special focus on molecular allergy diagnostics, Allergo J Int, 26, 93, 10.1007/s40629-017-0014-2 · DOI
  112. Larenas-Linnemann, 2017, Debates in Allergy Medicine: allergy skin testing cannot be replaced by molecular diagnosis in the near future, World Allergy Organ J, 10, 32, 10.1186/s40413-017-0164-1 · DOI
  113. Jensen-Jarolim, 2017, Debates in allergy medicine: molecular allergy diagnosis with ISAC will replace screenings by skin prick test in the future, World Allergy Organ J, 10, 33, 10.1186/s40413-017-0162-3 · DOI
  114. Scala, 2018, Cosensitization to profilin is associated with less severe reactions to foods in nsLTPs and storage proteins reactors and with less severe respiratory allergy, Allergy, 73, 1921, 10.1111/all.13501 · DOI
  115. Minami, 2015, IgE Abs to Der p 1 and Der p 2 as diagnostic markers of house dust mite allergy as defined by a bronchoprovocation test, Allergol Int, 64, 90, 10.1016/j.alit.2014.08.004 · DOI
  116. Stremnitzer, 2015, Papain degrades tight junction proteins of human keratinocytes in vitro and sensitizes C57bl/6 mice via the skin independent of its enzymatic activity or TLR4 activation, J Investig Dermatol, 135, 1790, 10.1038/jid.2015.58 · DOI
  117. Celi, 2019, House dust mite allergy in Italy-Diagnostic and clinical relevance of Der p 23 (and of minor allergens): a real-life, multicenter study, Allergy, 74, 1787, 10.1111/all.13776 · DOI
  118. Banerjee, 2015, Der p 11 is a major allergen for house dust mite-allergic patients suffering from atopic dermatitis, J Investig Dermatol, 135, 102, 10.1038/jid.2014.271 · DOI
  119. Zeng, 2015, Component-resolved diagnostic study of Dermatophagoides pteronyssinus major allergen molecules in a southern Chinese cohort, J Investig Allergol Clin Immunol, 25, 343
  120. Farioli, 2017, Mite-induced asthma and IgE levels to shrimp, mite, tropomyosin, arginine kinase, and der p 10 are the most relevant risk factors for challenge-proven shrimp allergy, Int Arch Allergy Immunol, 174, 133, 10.1159/000481985 · DOI
  121. Sanchez-Borges, 2019, Diagnosis of allergic sensitization in patients with allergic rhinitis and asthma in a tropical environment, Rev Alerg Mex, 66, 44, 10.29262/ram.v66i1.570 · DOI
  122. Ahumada, 2015, IgE responses to Ascaris and mite tropomyosins are risk factors for asthma, Clin Exp Allergy, 45, 1189, 10.1111/cea.12513 · DOI · Paper page
  123. Buendia, 2015, The IgE response to Ascaris molecular components is associated with clinical indicators of asthma severity, World Allergy Organ J, 8, 8, 10.1186/s40413-015-0058-z · DOI
  124. Camargo Lopes de Oliveira, 2019, rBlo t 5 is a potential contributor to the severity of atopic dermatitis in a Brazilian population, Pediatr Allergy Immunol, 30, 575, 10.1111/pai.13050 · DOI
  125. Chen, 2019, Selection of house dust mite-allergic patients by molecular diagnosis may enhance success of specific immunotherapy, J Allergy Clin Immunol, 143, 1248, 10.1016/j.jaci.2018.10.048 · DOI
  126. Sanchez-Borges, 2015, Hidden allergens and oral mite anaphylaxis: the pancake syndrome revisited, Curr Opin Allergy Clin Immunol, 15, 337, 10.1097/ACI.0000000000000175 · DOI
  127. Scala, 2017, Molecular recognition profiles and clinical patterns of PR-10 sensitization in a birch-free mediterranean area, Int Arch Allergy Immunol, 173, 138, 10.1159/000477565 · DOI · Paper page
  128. Moreira, 2015, Allergen microarray indicates pooideae sensitization in Brazilian grass pollen allergic patients, PLoS One, 10, 10.1371/journal.pone.0128402 · DOI
  129. Teifoori, 2014, Identification of the main allergen sensitizers in an Iran asthmatic population by molecular diagnosis, Allergy Asthma Clin Immunol, 10, 41, 10.1186/1710-1492-10-41 · DOI
  130. Hatzler, 2012, Molecular spreading and predictive value of preclinical IgE response to Phleum pratense in children with hay fever, J Allergy Clin Immunol, 130, 894, 10.1016/j.jaci.2012.05.053 · DOI
  131. Savi, 2013, Association between a low IgE response to Phl p 5 and absence of asthma in patients with grass pollen allergy, Clin Mol Allergy, 11, 3, 10.1186/1476-7961-11-3 · DOI
  132. Bokanovic, 2013, Determination of sIgE to rPhl p 1 is sufficient to diagnose grass pollen allergy, Allergy, 68, 1403, 10.1111/all.12263 · DOI
  133. Gao, 2019, Artemisia pollen allergy in China: component-resolved diagnosis reveals allergic asthma patients have significant multiple allergen sensitization, Allergy, 74, 284, 10.1111/all.13597 · DOI
  134. Armentia, 2015, Component-resolved diagnostics in vernal conjunctivitis, Ann Allergy Asthma Immunol, 115, 446, 10.1016/j.anai.2015.08.004 · DOI
  135. Quirce, 2009, Asthma in alergologica-2005, J Investig Allergol Clin Immunol, 19, 14
  136. Heinzerling, 2009, GA(2)LEN skin test study I: GA(2)LEN harmonization of skin prick testing: novel sensitization patterns for inhalant allergens in Europe, Allergy, 64, 1498, 10.1111/j.1398-9995.2009.02093.x · DOI · Paper page
  137. Konradsen, 2015, Allergy to furry animals: new insights, diagnostic approaches, and challenges, J Allergy Clin Immunol, 135, 616, 10.1016/j.jaci.2014.08.026 · DOI
  138. Smith, 2016, Dog allergen immunotherapy: past, present, and future, Ann Allergy Asthma Immunol, 116, 188, 10.1016/j.anai.2015.12.006 · DOI
  139. Cabanas, 2000, Importance of albumin in cross-reactivity among cat, dog and horse allergens, J Investig Allergol Clin Immunol, 10, 71
  140. Basagana, 2008, Allergy to human seminal fluid: cross-reactivity with dog dander, J Allergy Clin Immunol, 121, 233, 10.1016/j.jaci.2007.10.008 · DOI
  141. Khurana, 2016, The NPC2 protein: a novel dog allergen, Ann Allergy Asthma Immunol, 116, 440, 10.1016/j.anai.2016.02.006 · DOI
  142. Liccardi, 2015, What could be the role of molecular-based allergy diagnostics in detecting the risk of developing allergic sensitization to furry animals?, Eur Ann Allergy Clin Immunol, 47, 163
  143. Asarnoj, 2016, Sensitization to cat and dog allergen molecules in childhood and prediction of symptoms of cat and dog allergy in adolescence: a BAMSE/MeDALL study, J Allergy Clin Immunol, 137, 813, 10.1016/j.jaci.2015.09.052 · DOI · Paper page
  144. Bjerg, 2015, A population-based study of animal component sensitization, asthma, and rhinitis in schoolchildren, Pediatr Allergy Immunol, 26, 557, 10.1111/pai.12422 · DOI
  145. Nagao, 2017, Sensitization to secretoglobin and lipocalins in a group of young children with risk of developing respiratory allergy, Clin Mol Allergy, 15, 4, 10.1186/s12948-017-0061-8 · DOI
  146. Kack, 2018, Molecular allergy diagnostics refine characterization of children sensitized to dog dander, J Allergy Clin Immunol, 142, 1113, 10.1016/j.jaci.2018.05.012 · DOI
  147. Uriarte, 2016, Clinical relevance of molecular diagnosis in pet allergy, Allergy, 71, 1066, 10.1111/all.12917 · DOI · Paper page
  148. Adedoyin, 2007, Cat IgA, representative of new carbohydrate cross-reactive allergens, J Allergy Clin Immunol, 119, 640, 10.1016/j.jaci.2006.11.637 · DOI
  149. Barbosa, 2013, Efficacy of recombinant allergens for diagnosis of cockroach allergy in patients with asthma and/or rhinitis, Int Arch Allergy Immunol, 161, 213, 10.1159/000346318 · DOI
  150. Fang, 2015, Two new types of allergens from the cockroach, Periplaneta americana, Allergy, 70, 1674, 10.1111/all.12766 · DOI
  151. Tanimoto, 2015, Molecular-based allergy diagnosis of allergic bronchopulmonary aspergillosis in Aspergillus fumigatus-sensitized Japanese patients, Clin Exp Allergy, 45, 1790, 10.1111/cea.12590 · DOI
  152. Balenga, 2015, A fungal protease allergen provokes airway hyper-responsiveness in asthma, Nat Commun, 6, 6763, 10.1038/ncomms7763 · DOI
  153. Muthu, 2018, Utility of recombinant Aspergillus fumigatus antigens in the diagnosis of allergic bronchopulmonary aspergillosis: a systematic review and diagnostic test accuracy meta-analysis, Clin Exp Allergy, 48, 1107, 10.1111/cea.13216 · DOI
  154. Pali-Scholl, 2018, The effect of digestion and digestibility on allergenicity of food, Nutrients, 10, 10.3390/nu10091129 · DOI
  155. Simons, 2012, 2012 update: world allergy organization guidelines for the assessment and management of anaphylaxis, Curr Opin Allergy Clin Immunol, 12, 389, 10.1097/ACI.0b013e328355b7e4 · DOI
  156. Antonicelli, 2014, Component resolved diagnosis in real life: the risk assessment of food allergy using microarray-based immunoassay, Eur Ann Allergy Clin Immunol, 46, 30
  157. Lopez-Matas, 2015, Tomato nsLTP as an “in vivo" diagnostic tool: sensitization in a Mediterranean population, J Investig Allergol Clin Immunol, 25, 196
  158. Scala, 2015, Lipid transfer protein sensitization: reactivity profiles and clinical risk assessment in an Italian cohort, Allergy, 70, 933, 10.1111/all.12635 · DOI
  159. Pascal, 2016, Asymptomatic LTP sensitisation is common in plant-food allergic children from the Northeast of Spain, Allergol Immunopathol, 44, 351, 10.1016/j.aller.2015.10.003 · DOI
  160. Vieira, 2014, Diagnostic usefulness of component-resolved diagnosis by skin prick tests and specific IgE to single allergen components in children with allergy to fruits and vegetables, Allergol Immunopathol, 42, 127, 10.1016/j.aller.2012.09.001 · DOI
  161. Patelis, 2016, Multiplex component-based allergen microarray in recent clinical studies, Clin Exp Allergy, 46, 1022, 10.1111/cea.12761 · DOI · Paper page
  162. Peveri, 2019, Molecular diagnostics improves diagnosis and treatment of respiratory allergy and food allergy with economic optimization and cost saving, Allergol Immunopathol (Madr), 47, 64, 10.1016/j.aller.2018.05.008 · DOI
  163. Kuitunen, 2015, High IgE levels to alpha-lactalbumin, beta-lactoglobulin and casein predict less successful cow's milk oral immunotherapy, Allergy, 70, 955, 10.1111/all.12647 · DOI
  164. Sato, 2015, A review of biomarkers for predicting clinical reactivity to foods with a focus on specific immunoglobulin E antibodies, Curr Opin Allergy Clin Immunol, 15, 250, 10.1097/ACI.0000000000000162 · DOI
  165. Petersen, 2018, Cow's milk allergic children-Can component-resolved diagnostics predict duration and severity?, Pediatr Allergy Immunol, 29, 194, 10.1111/pai.12854 · DOI
  166. Bartuzi, 2017, Contribution of molecular allergen analysis in diagnosis of milk allergy, Curr Allergy Asthma Rep, 17, 46, 10.1007/s11882-017-0716-z · DOI
  167. Agyemang, 2019, Utilizing boiled milk sIgE as a predictor of baked milk tolerance in cow's milk allergic children, J Allergy Clin Immunol Pract, 7, 2049, 10.1016/j.jaip.2019.01.034 · DOI
  168. Kim, 2014, Special consideration is required for the component-resolved diagnosis of egg allergy in infants, Ann Allergy Asthma Immunol, 112, 53, 10.1016/j.anai.2013.09.010 · DOI
  169. Dang, 2019, Egg allergen specific IgE diversity predicts resolution of egg allergy in the population cohort HealthNuts, Allergy, 74, 318, 10.1111/all.13572 · DOI
  170. Petrosino, 2018, Usefulness of molecular diagnosis in egg allergic children, Arch Med Sci, 14, 132, 10.5114/aoms.2016.58796 · DOI
  171. Faber, 2016, Sensitization profiles to peanut allergens in Belgium; cracking the code in infants, children and adults, Acta Clin Belg, 71, 32, 10.1080/17843286.2015.1109170 · DOI
  172. Giovannini, 2019, Retrospective definition of reaction risk in Italian children with peanut, hazelnut and walnut allergy through component-resolved diagnosis, Allergol Immunopathol, 47, 73, 10.1016/j.aller.2018.03.009 · DOI
  173. Ackerbauer, 2015, Component-resolved IgE profiles in Austrian patients with a convincing history of peanut allergy, Int Arch Allergy Immunol, 166, 13, 10.1159/000371422 · DOI
  174. Kukkonen, 2015, Ara h 2 and Ara 6 are the best predictors of severe peanut allergy: a double-blind placebo-controlled study, Allergy, 70, 1239, 10.1111/all.12671 · DOI
  175. Ballmer-Weber, 2015, IgE recognition patterns in peanut allergy are age dependent: perspectives of the EuroPrevall study, Allergy, 70, 391, 10.1111/all.12574 · DOI
  176. Suratannon, 2013, Component-resolved diagnostics for the evaluation of peanut allergy in a low-prevalence area, Pediatr Allergy Immunol, 24, 665, 10.1111/pai.12125 · DOI
  177. Amoah, 2013, Peanut-specific IgE antibodies in asymptomatic Ghanaian children possibly caused by carbohydrate determinant cross-reactivity, J Allergy Clin Immunol, 132, 639, 10.1016/j.jaci.2013.04.023 · DOI
  178. Lopes de Oliveira, 2013, The value of specific IgE to peanut and its component Ara h 2 in the diagnosis of peanut allergy, J Allergy Clin Immunol Pract, 1, 394, 10.1016/j.jaip.2013.05.010 · DOI
  179. Lu, 2018, Combining 2-DE immunoblots and mass spectrometry to identify putative soybean (Glycine max) allergens, Food Chem Toxicol, 116, 207, 10.1016/j.fct.2018.04.032 · DOI
  180. Ebisawa, 2013, Gly m 2S albumin is a major allergen with a high diagnostic value in soybean-allergic children, J Allergy Clin Immunol, 132, 976, 10.1016/j.jaci.2013.04.028 · DOI
  181. Klemans, 2013, Components in soy allergy diagnostics: Gly m 2S albumin has the best diagnostic value in adults, Allergy, 68, 1396, 10.1111/all.12259 · DOI
  182. Datema, 2015, Hazelnut allergy across Europe dissected molecularly: a EuroPrevall outpatient clinic survey, J Allergy Clin Immunol, 136, 382, 10.1016/j.jaci.2014.12.1949 · DOI
  183. Buyuktiryaki, 2016, Cor a 14, hazelnut-specific IgE, and SPT as a reliable tool in hazelnut allergy diagnosis in eastern mediterranean children, J Allergy Clin Immunol Pract, 4, 265, 10.1016/j.jaip.2015.12.012 · DOI
  184. Masthoff, 2013, Sensitization to Cor a 9 and Cor a 14 is highly specific for a hazelnut allergy with objective symptoms in Dutch children and adults, J Allergy Clin Immunol, 132, 393, 10.1016/j.jaci.2013.02.024 · DOI
  185. Brandstrom, 2015, Basophil allergen threshold sensitivity and component-resolved diagnostics improve hazelnut allergy diagnosis, Clin Exp Allergy, 45, 1412, 10.1111/cea.12515 · DOI
  186. Villalta, 2018, Evidence of cross-reactivity between different seed storage proteins from hazelnut (corylus avellana) and walnut (juglans regia) using recombinant allergen proteins, Int Arch Allergy Immunol, 1
  187. Datema, 2018, Component-resolved diagnosis and beyond: multivariable regression models to predict severity of hazelnut allergy, Allergy, 73, 549, 10.1111/all.13328 · DOI
  188. Beck, 2018, The concordance between component tests and clinical history in British adults with suspected pollen-food syndrome to peanut and hazelnut, J Clin Pathol, 71, 239, 10.1136/jclinpath-2017-204573 · DOI
  189. Sievers, 2016, Wheat protein recognition pattern in tolerant and allergic children, Pediatr Allergy Immunol, 27, 147, 10.1111/pai.12502 · DOI
  190. Makela, 2014, Wheat allergy in children - new tools for diagnostics, Clin Exp Allergy, 44, 1420, 10.1111/cea.12393 · DOI
  191. Koike, 2018, Predictors of persistent wheat allergy in children: a retrospective cohort study, Int Arch Allergy Immunol, 176, 249, 10.1159/000489337 · DOI
  192. Yanagida, 2018, Increasing specific immunoglobulin E levels correlate with the risk of anaphylaxis during an oral food challenge, Pediatr Allergy Immunol, 29, 417, 10.1111/pai.12896 · DOI
  193. Kennard, 2018, A multicenter evaluation of diagnosis and management of omega-5 gliadin allergy (also known as wheat-dependent exercise-induced anaphylaxis) in 132 adults, J Allergy Clin Immunol Pract, 6, 1892, 10.1016/j.jaip.2018.02.013 · DOI
  194. Safi, 2019, Identification and molecular characterization of allergenic non-specific lipid-transfer protein from durum wheat (Triticum turgidum), Clin Exp Allergy, 49, 120, 10.1111/cea.13271 · DOI
  195. Sander, 2015, Component-resolved diagnosis of baker's allergy based on specific IgE to recombinant wheat flour proteins, J Allergy Clin Immunol, 135, 1529, 10.1016/j.jaci.2014.11.021 · DOI
  196. Geiselhart, 2018, Concomitant sensitization to legumin, Fag e 2 and Fag e 5 predicts buckwheat allergy, Clin Exp Allergy, 48, 217, 10.1111/cea.13068 · DOI
  197. Yanagida, 2018, Specific IgE for Fag e 3 Predicts Oral Buckwheat Food Challenge Test Results and Anaphylaxis: a Pilot Study, Int Arch Allergy Immunol, 176, 8, 10.1159/000487135 · DOI
  198. Einhorn, 2018, Molecular allergen profiling in horses by microarray reveals Fag e 2 from buckwheat as a frequent sensitizer, Allergy, 73, 1436, 10.1111/all.13417 · DOI
  199. Caimmi, 2013, Understanding the molecular sensitization for Cypress pollen and peach in the Languedoc-Roussillon area, Allergy, 68, 249, 10.1111/all.12073 · DOI
  200. Mothes-Luksch, 2017, Pru p 3, a marker allergen for lipid transfer protein sensitization also in Central Europe, Allergy, 72, 1415, 10.1111/all.13151 · DOI

200 of 315 shown

Cited by

Sorted by citations

See all 122

Metadata

Authors
Ansotegui, I. J., Melioli, G., Canonica, G. W., Gómez, R. M., Jensen-Jarolim, E., Ebisawa, M., Luengo, O., Caraballo, L., Passalacqua, G., Poulsen, L. K., Savi, E., Zuberbier, T., Villa, E., Oppenheimer, J., Asero, R., Bernstein, J., Bousquet, J., Cardona, V., Cox, L., Demoly, P., Ferreira, F., Giavina Bianchi, P., Gonzalez Diaz, S., Jakob, T., Kase Tanno, L., Kleine-Tebbe, J., Levin, M., Martin, B., Matricardi, P. M., Monge Ortega, O. P., Morais Almeida, M., Nunes, C., Ortega Martell, J. A., Pawankar, R., Renz, H., Rosário Filho, N., Rouadi, P., Ruiba, A., Sampson, H., Sánchez Borges, M., Scala, E., Schmid-Grendelmeier, P., Senna, G.-E., Sisul, J. C., Tang, M. L. K., Valenta, R., van Hage, M., Wong, G. W. K., & Yáñez, A.
Venue
World Allergy Organization Journal
Publisher
Elsevier BV
Published
2020-02
Volume
13
Issue
2
Pages
100091
ISSN
1939-4551
DOI
10.1016/j.waojou.2019.100091
PMC
PMC7062937
Cited by
122
References
17
Language
en
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: A WAO—ARIA—GA2LEN Consensus Document on Molecular-Based Allergy Diagnosis (PAMD@): Update 2020. https://app.cochat.ai/papers/10.1016/j.waojou.2019.100091
The paper
Ansotegui, I. J., Melioli, G., Canonica, G. W., Gómez, R. M., Jensen-Jarolim, E., Ebisawa, M., Luengo, O., Caraballo, L., Passalacqua, G., Poulsen, L. K., Savi, E., Zuberbier, T., Villa, E., Oppenheimer, J., Asero, R., Bernstein, J., Bousquet, J., Cardona, V., Cox, L., . . . Yáñez, A. (2020). A WAO—ARIA—GA2LEN Consensus Document on Molecular-Based Allergy Diagnosis (PAMD@): Update 2020. World Allergy Organization Journal. https://doi.org/10.1016/j.waojou.2019.100091