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BioMed Research International
Volume 2013 (2013), Article ID 746507, 9 pages
IgE Sensitization to the Nonspecific Lipid-Transfer Protein Ara h 9 and Peanut-Associated Bronchospasm
1Institute of Inflammation and Repair, University of Manchester, Manchester M13 9WL, UK
2Department of Paediatric Allergy & Immunology, Royal Manchester Children’s Hospital, University of Manchester, Oxford Road, Manchester M13 9WL, UK
3Department of Immunology, Salford Royal Foundation Trust, Manchester M6 8HD, UK
Received 10 April 2013; Revised 21 July 2013; Accepted 12 August 2013
Academic Editor: Laurian Zuidmeer-Jongejan
Copyright © 2013 Peter D. Arkwright et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Allergen component analysis is now available in many laboratories. The aim of this study was to examine the possible association between peanut allergen IgE components and severity of clinical reactions in patients with a history of peanut allergy. Data and sera collected from 192 patients within the Manchester Allergy Research Database and Serum Bank were used in this retrospective study. Sensitization to peanut specific IgE and Ara h 1, 2, 3, and 8 peanut IgE components, as measured by fluoroenzyme immunoassay, was not associated with anaphylaxis. In contrast, sensitization to the lipid-transfer protein Ara h 9 was significantly more prevalent in patients with peanut-associated bronchospasm (26% versus 9% of patients), even after adjusting for potential confounding effects of age, gender, and severity of concomitant chronic atopic diseases. Patients who were sensitized to Ara h 9 were more likely to have ingested rather than just have had skin contact with peanut and have a more rapid onset of symptoms. These results are consistent with observations that sensitization to heat and protease resistant lipid-transfer protein components of hazelnut, grains, and fruit is predictive of anaphylaxis.
Approximately 1/100 individuals in Western countries suffer from peanut allergy . Peanut is a leading cause of food-induced anaphylaxis, defined as a serious allergic reaction that is rapid in onset and may cause death through respiratory or circulatory failure [2–4]. Adolescences and young adults, as well as those with severe asthma, are prone to more severe reactions . Skin prick tests and serum specific IgE concentrations are markers of immune sensitization. Thirteen specific allergic protein components of peanut have now been identified and characterized [6, 7]. Ara h 2 is the predominant antigen in peanut-allergic patients in some but not all countries. It may also help to predict the likelihood of clinical reactivity in patients without a clinical history of peanut allergy [8–11]. Ara h 1, 3, and 6 are other seed storage proteins that commonly induce IgE responses [12, 13]. Ara h 8 is a heat and enzyme-labile pathogenesis-related protein (PR-10) with cross-reacting antigenic epitopes to birch tree pollen allergen Bet v 1. Because of its degradation by salivary and gastric juices, IgE-mediated reactions to PR-10 allergens are commonly localized to the oral cavity [14–16]. In contrast, Ara h 9 is a heat and enzyme-stable nonspecific lipid transfer protein (nsLTP) with cross-reacting epitopes to other nsLTP such as hazelnut (Cor a 8) and peach (Pru p 3) .
Allergen analysis to these components is increasingly available in clinical immunology laboratories around the world. There are data to suggest that this technology might predict peanut allergy in selected patients without the need for oral challenges [8, 18]. However, at present there is no evidence that it can predict the risk of life-threatening anaphylaxis. The Manchester Allergy Research Database has detailed, standardised, clinical data on the severity of clinical reactions in patients with peanut allergy. The current study aims to address the question as to whether component analysis can predict the risk of anaphylaxis defined as clinical features of respiratory or circulatory compromise in patients with documented clinical peanut allergy.
Clinical details of patients with peanut allergy attending a regional allergy clinic at Manchester Royal Infirmary, Manchester, UK between 1992 to 2004 were recorded onto structured history forms by allergy specialists (PDA and RSP). All patients were referred by primary care physicians or general pediatricians. The diagnosis was made on the basis specialists’ clinical history of allergic reaction to peanuts or peanut containing food taken at the consultation, supported by either evidence from skin prick tests or raised allergen specific serum IgE concentrations. Allergic symptoms were carefully documented, particularly acute respiratory or circulatory symptoms occurring after eating the food indicative of more serious reactions (anaphylaxis). Pharyngeal edema was considered in patients with a hoarse voice, difficulty swallowing, and/or difficulty breathing. Bronchospasm was considered if patients were wheezy. Reduced (dizziness/light headedness) loss of consciousness were considered features of circulatory insufficiency.
Patients were classified as having atopic dermatitis if they fulfilled the British Association of Dermatologists Working Party Criteria and required topical corticosteroids or calcineurin antagonists for control of their symptoms. Patients with moderate-severe asthma were those with wheeze requiring inhaled corticosteroids and/or leukotriene antagonists in addition to inhaled bronchodilators. Patients with allergic rhinitis had sneezing, itchy eyes, nasal congestion, and rhinorrhea requiring oral antihistamines or topical intranasal steroids. Clinical details were also recorded as to the date of reaction in relation to consultation, the amount of food consumed and the delay between consuming the food and the onset of the reaction.
All patients were otherwise well and were not on regular β-blockers, other antihypertensives, or antidepressants. Serum for measurement of total and allergen specific IgE (sIgE) was taken at the initial consultation and stored at −40°C in a centralized serum bank before processing. All patients signed a written consent form, and the collection of data and serum had the approval of the Local Research Ethics Committee (04/Q1401/44).
2.2. Serum IgE Measurements
Total serum IgE concentrations, peanut (peanut specific, Ara h 1, Ara h 2, Ara h 3, Ara h 8, Ara h 9 allergen components), tree nut specific (almond, brazil, cashew, hazelnut, cashew), and cross-reacting allergen component (Bet v 1 from birch, Cor a 1 and Cor a 8 from hazelnut, Pru p 3 from peach) IgE were measured by fluoroenzymeimmunoassay using the automated ImmunoCAP250 processor (Thermo Scientific (formerly Phadia Ltd), UK). Timothy grass pollen components Phl p 1, 4, 5B, 7, and 12 were also measured. Total IgE is quoted as kilounits per litre (kU/L) and sIgE units as allergen specific kilounits per litre (kUA/L). Sensitization was defined as patients with peanut or peanut component sIgE concentrations ≥0.35 kUA/L.
2.3. Statistical Analysis
Data from the centralized Access database were entered into an SPSS spreadsheet (IBM SPSS Statistics 20, Chicago, Ill). The sample size had an 80% power to detect 2.5-fold differences between patients with and without symptoms of anaphylaxis with a two-tailed P value of 0.05. As some data were not normally distributed, continuous variables are quoted as median (interquartile range). Initially, Chi-square and Mann-Whitney tests were used to detect statistical differences between groups. Covariant analyses examining the relative effect of a number of variables at the same time as shown in Tables 2 and 3 were performed using multinominal logistic regression. In this statistical model, symptoms of (i) pharyngeal edema (none, hoarse voice (mild), or drooling and dyspnea (moderate-severe)); (ii) bronchospasm (none, wheeze (mild), wheeze with dyspnea (moderate-severe)); or (iii) circulatory insufficiency (none, dizziness (mild), loss of consciousness (moderate-severe)) were the discrete independent variable used in three separate analyses. Discrete covariants used in the regression equations were: child or adult; gender; atopic dermatitis; asthma; allergic rhinitis; sensitization (defined as ≥0.35 kUA/L) to peanut IgE, peanut allergen components Ara h 1, Ara h 2, Ara h 3, Ara h 8, Ara h 9, Timothy grass allergen components Phl p 1, Phl p 4, Phl p 5B, Phl p 12. Results are expressed as Relative Risk and 95% confidence intervals. Results are expressed as Relative Risk and 95% confidence intervals.
3. Results and Discussion
3.1. Clinical Features and Severity of Acute and Chronic Allergic Diseases
192 patients with peanut allergy and a median age of five years (inter-quartile range 2 to 10 years) were studied (Table 1). The median (interquartile range) interval between the reaction and seeing the patient and collecting blood was 15 (3–38) months. Peanut-containing foods causing the reaction were whole nuts in 56%, biscuit/cake/cereal in 17%, chocolates in 16%, and Chinese/Indian/Italian food in 6%. 32% of patients had a history of reacting to other foods, in 15% tree nuts and in 11% milk, egg, or fish. Median (inter-quartile range) onset of symptoms after eating the food was two (1 to 10) minutes. Time from onset to peak symptoms was 15 (10 to 30) minutes.
63% patients developed symptoms of upper respiratory, lower respiratory, or altered conscious level. 88% suffered from moderate to severe chronic atopic disease (atopic dermatitis, asthma, and or allergic rhinoconjunctivitis). 40% had two of these conditions, and 20% had all three.
3.2. Clinical and Laboratory Parameters Associated with More Severe Allergic Symptoms
The possible associations between respiratory symptoms/altered consciousness and age, gender, presence or absence of chronic atopic diseases and IgE parameters were investigated (Tables 2 and 3). The extent of exposure to peanut-containing food ingested did not correlate with severity of allergic reaction.
Patients with symptoms of pharyngeal edema were significantly older (median (inter-quartile) age 8 (4 to 16) years) than those with no symptoms (3 (1 to 6) years; ). They were also 3-4 times more likely to have allergic rhinitis (Table 2). An association with asthma was significant only in patients with severe pharyngeal symptoms such as drooling and dyspnea. Sensitization to peanut sIgE or peanut and Timothy grass pollen allergen components (≥0.35 kUA/L) was not associated with clinical symptoms of pharyngeal edema, even after adjusting for the potential confounding effects of clinical and laboratory cofactors using multinominal regression analysis.
Patients with symptoms of acute bronchospasm were significantly older (6 (3 to 13) years) than those with no bronchospasm (3 (1 to 8); ). They were also significantly more likely to have asthma requiring regular inhaled corticosteroids (Table 3) but not milder asthma requiring intermittent bronchodilators (data not shown). Patients who developed severe wheeze associated with dyspnea were also significantly more likely to have allergic rhinitis. Patients sensitized to Ara h 9, but not other peanut allergen components, were more likely to have symptoms of bronchospasm than those who were not sensitized (26% versus 9%; ). 73% of the 33 patients who had Ara h 9 ≥0.35 kUA/L (median (range): 1.23 (0.41 to 35.7) /L) had bronchospasm compared with 43% of patients who were not Ara h 9 sensitized (). Although Ara h 9 sensitized patients were significantly older (8 (4–16) versus 4 (2–8) years; ), the association between bronchospasm and Ara h 9 sensitization remained significant even after adjusting for age, as well as other potential confounding factors, such as gender, chronic atopic diseases, and cosensitization with other peanut, or Timothy grass pollen allergen components.
Compared with children (9%), significantly more adults became dizzy (23%) or lost consciousness (50%) (). None of the other clinical (gender, history of atopic disease) or peanut sIgE/allergen component IgE showed a significant correlation (data not shown).
In this cohort, there was also no association between asthma and IgE sensitization to Ara h 9 or any other peanut component (data not shown). Patients with respiratory symptoms or altered consciousness did not have significantly higher peanut specific or peanut allergen component IgE concentrations than patients who did not have these clinical features. Patients with evidence of IgE sensitized to Ara h 1, 2, and 3 storage proteins were not more likely to develop respiratory symptoms or faintness than those who were not sensitized to any one of these components.
Key clinical parameters relating to the allergic reaction were compared in patients sensitized to Ara h 2 and Ara h 9 (Figure 1). Patients who were sensitized to Ara h 2 were not significantly older, more likely to have ingested peanut rather than just have skin contact, have a shorter time to onset or peak reaction than those who were not sensitized (Figure 1(a)). In contrast, significantly more Ara h 9 sensitized patients had a history of ingestion rather than just skin contact with peanut (), and 50% of Ara h 9 sensitized patients had an onset of symptoms within five minutes of contact compared with only 23% of patients who were not sensitized (). Time from onset to peak symptoms was however not significantly different in Ara h 9 sensitized and nonsensitized patients.
3.3. Cross-Sensitization between Peanut and Pollen Allergen Components
84% of patients were peanut specific IgE positive and of this group, 82% were Ara 1, 2, or 3 positive. 75% were Ara h 2 positive, 46% were Ara h 1 positive, and 36% were Ara h 3 positive (Figure 2(a)). All of the 33 patients (18%) who showed no IgE sensitization to Ara h 1, 2, and 3 were peanut skin prick test positive with wheals of 4–25 mm.
Sensitization to Ara h 8 and 9 was less common, being 21% and 20% of the total cohort, respectively. The Ara h 8 component of peanut is a PR-10 pathogenesis-related protein, which may cross-react with other PR-10 proteins, such as Bet v 1 from Birch pollen and Cor a 1 from hazelnut. There was a strong correlation between sensitization to these three components. 14% of the total cohort was positive to all three allergen components, and 70% were negative to all three components, leaving only 16% where there was any discordance (Figure 2(b)). Of the patients that were Ara h 8 sensitized, the median (IQR) concentrations were higher for both Bet v 1 13.4 (2.8–22.7) kUA/L and Cor a 1 9.7 (5.3–16.7 kUA/L) components than for Ara h 8 (2.3 (1.3–7.0) /L). Although PR-10 pathogenesis-related proteins, 80–100% of patients were not considered sensitized to Ara h 8 were also sensitized to Ph p 1, Phl p 4, Phl p 5B, and Phl p 12 components of Timothy grass pollen () (Table 4).
Ara h 9 is a nsLTP, as are Pru p 3 (peach allergen component) and Cor a 8 (hazelnut allergen component). 13% of the cohort was positive to all three allergen components, and 78% were negative to all three components, leaving only 9% where there was any discordance (Figure 2(c)). Of the patients that were Ara h 9 sensitized, the median (IQR) concentrations were higher for both Pru p 3 5.1 (1.7–10.5) /L and Cor a 8 1.8 (0.5–3.4 kUA/L) components than for Ara h 9 (0.8 (0.4–1.8) /L). Although an nsLTP protein was not considered, 50% of patients sensitized to Ara h 9 were also sensitized to the Phl p 12 component of grass pollen, while 92% of patients who were not sensitized to Ara h 9 were negative to Phl p 12 () (Table 4). None of the other Timothy grass pollen components showed such a significant association with Ara h 9.
3.4. Interpretation and Relationship of the Results to Previous Studies
In patients with peanut allergy, the nsLTP peanut component Ara h 9 was associated with a significantly higher risk of bronchospasm but not pharyngeal edema or altered consciousness. In this cohort, there was no association between reaction severity and other peanut components (Ara h 1, 2, 3, and 8). In particular, although Ara h 2 was the predominant allergen component, Ara h 2 sensitization did not predict severity of respiratory or circulatory symptoms.
Previous studies have suggested that Ara h 9 is a more important peanut allergen in Mediterranean countries than other parts of the world . Although only one in ten patients in our cohort was sensitized to Ara h 9, it also appears to be clinically relevant to Northern European populations. The observed association between Ara h 9 and peanut-associated bronchospasm supports the growing appreciation of LTP-associated food-induced anaphylaxis as an important subgroup of food allergy [20–27]. This contrasts with oral allergy syndrome associated with sensitization to the heat and enzyme labile PR-10 allergens such as Bet v 1-like allergen components . The latter group of patients often also have Birch-pollinosis, while the former group may not. In our study, sensitization to Ara h 8 (a Bet v 1 homologue) was not associated with milder symptoms, probably because of the overlap between sensitization to this and other peanut components. As only 6% of the 192 patients in our cohort were sensitized to Ara h 8 alone, subgroup analysis was not feasible.
Protein allergens within the LTP family are known to have high levels of sequence homology and thus IgE cross-sensitization. An example is Ara h 9 derived from peanut and Pru p 3 from peach where the sequence homology is 62–68% . It is therefore not surprising that we found 91% concordance in cross-sensitization between three LTPs: Ara h 9, Pru p 3, and Cor a 8, the LTP from hazelnut. Only 5 (3%) of patients in this cohort had a clinical history of allergy to hazelnut and only one had reacted to peach, indicating that peanut rather than peach or hazelnut is likely to be triggering the cross-sensitization to these nsLTPs. Similarly high sequence homology is found in PR-10 proteins and we found that the IgE sensitization concordance of the PR-10 homologues of peanut (Ara h 8), hazelnut (Cor a 1), and birch pollen (Bet v 1) was just as high at 86%. Although this study found that the peanut Ara h 9 IgE component concentration was lower than food and pollen homologs, direct comparisons between allergens should be made cautiously, as specific IgE thresholds associated with risk of clinical reactions are known to vary .
Timothy grass pollen allergen components are also known to cross-react with peanut components, but in this study Timothy grass pollen components did not lead to any confounding effects in relation to the association between Ara h 9 and bronchospasm. Furthermore, there was no significant association detected between Phl p 12 the Timothy grass pollen component associated with Ara h 9 sensitization and severity of the allergic reaction, presence of concomitant atopic disease, age of the patients or timing of onset of the reaction.
As Ara h 9 sensitization was negative in 80% of the peanut allergic patients, measurement of this allergen component has a low sensitivity in predicting severe reactions to peanut. Ara h 9, and Ara h 1, 2, and 3 are antigenically stable, even after cooking, and therefore the fact that 39% of peanut was ingested in a cooked or processed form is unlikely to have influenced the results of this study . It has previously been shown that evidence of sensitization to the major peanut allergens remains stable over 20 months . There is no evidence of significant degradation of antigenic components after prolonged freezing, thus storage of the samples is unlikely to be a significant confounding factor. Additional subanalyses, which included only patients having a total IgE of >60 kU/L, gave similar results and thus provided evidence that the lack of correlation was not due to false negative results because of low/normal total IgE concentrations in the cohort. None of the patients were taking medication which might have exaggerated the clinical symptoms and thus confounded the results.
Although formal oral challenge to peanut is a more objective measure of peanut allergy than clinical history taking, the former procedure is designed to start with amounts of the allergen that are unlikely to trigger a reaction, and it is classically discontinued at the first definite signs of allergy, usually urticaria or local facial angioedema rather than anaphylaxis. Thus, it is not ideal for determining factors associated with severe allergic reactions/anaphylaxis. Clinical history relies on recall of past events, and thus there may be concerns about its accuracy. The proformas used in this study and the fact that the two allergists did a number of clinics together to standardize data collection helped to keep any bias or variation in the way the information was collected from this cohort to a minimum.
In keeping with our previous study, clinical features of pharyngeal edema were more common particularly in patients with allergic rhinitis and bronchospasm more common in patients with asthma . We would therefore recommend that all patients with peanut allergy have their asthma and allergic rhinitis management optimised as a possible therapeutic measure to reduce the risk of peanut-induced anaphylaxis.
This study shows that IgE sensitization to the nsLTP Ara h 9 may be an important factor in determining the severity of bronchospasm in some patients with a history of peanut allergy. It is not the only factor as only 26% of patients with symptoms of bronchospasm were Ara h 9 positive and it is not specific as 9% of patients with no bronchospasm were sensitized to this component. In this regard, there is no evidence from this study that component analysis can replace clinical history, or where there is doubt about the history, replace formal oral challenge with peanut. The results do however fit with the growing body of evidence which suggests that LTP components of a number of foods are associated with clinical features of systemic allergic reactions. Our findings need to be verified in additional independent cohorts and if confirmed, the mechanisms linking Ara h 9 to severe allergy should be studied further.
Although this study was performed as an independent investigator project coordinated by PDA at the University of Manchester, the authors are grateful to Thermo Scientific Ltd. that kindly provided the reagents for peanut component analysis as well as contributing to the laboratory costs of analysing the samples. The authors declare no additional conflict of interests. The remaining funding for this study came from a PDA charitable University of Manchester account. The help of Janice Ditchfield, CSci, FIBMS, Department of Immunology, Salford Royal Foundation Trust in performing the IgE analyses is gratefully acknowledged.
- J. O. Hourihane, “Peanut allergy,” Pediatric Clinics of North America, vol. 58, no. 2, pp. 445–458, 2011.
- H. A. Sampson, A. Muñoz-Furlong, R. L. Campbell et al., “Second symposium on the definition and management of anaphylaxis: summary report—Second National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network Symposium,” Annals of Emergency Medicine, vol. 47, no. 4, pp. 373–380, 2006.
- S. A. Bock, A. Muoz-Furlong, and H. A. Sampson, “Fatalities due to anaphylactic reactions to foods,” Journal of Allergy and Clinical Immunology, vol. 107, no. 1, pp. 191–193, 2001.
- R. S. H. Pumphrey and M. H. Gowland, “Further fatal allergic reactions to food in the United Kingdom, 1999–2006,” Journal of Allergy and Clinical Immunology, vol. 119, no. 4, pp. 1018–1019, 2007.
- C. W. Summers, R. S. Pumphrey, C. N. Woods, G. McDowell, P. W. Pemberton, and P. D. Arkwright, “Factors predicting anaphylaxis to peanuts and tree nuts in patients referred to a specialist center,” Journal of Allergy and Clinical Immunology, vol. 121, no. 3, pp. 632–638, 2008.
- N. Nicolaou and A. Custovic, “Molecular diagnosis of peanut and legume allergy,” Current Opinion in Allergy and Clinical Immunology, vol. 11, no. 3, pp. 222–228, 2011.
- H. Breiteneder and C. Radauer, “A classification of plant food allergens,” Journal of Allergy and Clinical Immunology, vol. 113, no. 5, pp. 821–830, 2004.
- R. J. Klemans, D. Otte, M. Knol, et al., “The diagnostic value of specific IgE to Ara h 2 to predict peanut allergy in children is comparable to a validated and updated diagnostic prediction model,” Journal of Allergy and Clinical Immunology, vol. 131, pp. 157–163, 2013.
- N. Nicolaou, C. Murray, D. Belgrave, M. Poorafshar, A. Simpson, and A. Custovic, “Quantification of specific IgE to whole peanut extract and peanut components in prediction of peanut allergy,” Journal of Allergy and Clinical Immunology, vol. 127, no. 3, pp. 684–685, 2011.
- S. H. Sicherer, R. A. Wood, S. Abramson et al., “Allergy testing in childhood: using allergen-specific IgE tests,” Pediatrics, vol. 129, no. 1, pp. 193–197, 2012.
- A. Vereda, M. van Hage, S. Ahlstedt et al., “Peanut allergy: clinical and immunologic differences among patients from 3 different geographic regions,” Journal of Allergy and Clinical Immunology, vol. 127, no. 3, pp. 603–607, 2011.
- A. W. Burks, L. W. Williams, R. M. Helm, C. Connaughton, G. Cockrell, and T. O'Brien, “Identification of a major peanut allergen, Ara h I, in patients with atopic dermatitis and positive peanut challenges,” Journal of Allergy and Clinical Immunology, vol. 88, no. 2, pp. 172–179, 1991.
- P. Restani, C. Ballabio, E. Corsini et al., “Identification of the basic subunit of Ara h 3 as the major allergen in a group of children allergic to peanuts,” Annals of Allergy, Asthma and Immunology, vol. 94, no. 2, pp. 262–266, 2005.
- D. Mittag, J. Akkerdaas, B. K. Ballmer-Weber 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,” Journal of Allergy and Clinical Immunology, vol. 114, no. 6, pp. 1410–1417, 2004.
- A. Asarnoj, R. Movérare, E. Östblom et al., “IgE to peanut allergen components: relation to peanut symptoms and pollen sensitization in 8-year-olds,” Allergy, vol. 65, no. 9, pp. 1189–1195, 2010.
- B. Niggemann, R. Schmitz, and M. Schlaud, “The high prevalence of peanut sensitization in childhood is due to cross-reactivity to pollen,” Allergy, vol. 66, no. 7, pp. 980–981, 2011.
- I. Lauer, N. Dueringer, S. Pokoj et al., “The non-specific lipid transfer protein, Ara h 9, is an important allergen in peanut,” Clinical and Experimental Allergy, vol. 39, no. 9, pp. 1427–1437, 2009.
- L. Cox, “Overview of serological-specific IgE antibody testing in children,” Current Allergy and Asthma Reports, vol. 11, no. 6, pp. 447–453, 2011.
- S. Krause, G. Reese, S. Randow et al., “Lipid transfer protein (Ara h 9) as a new peanut allergen relevant for a Mediterranean allergic population,” Journal of Allergy and Clinical Immunology, vol. 124, no. 4, pp. 771–778, 2009.
- R. Asero, G. Mistrello, D. Roncarolo et al., “Lipid transfer protein: a pan-allergen in plant-derived foods that is highly resistant to pepsin digestion,” International Archives of Allergy and Immunology, vol. 122, no. 1, pp. 20–32, 2000.
- M. Egger, M. Hauser, A. Mari, F. Ferreira, and G. Gadermaier, “The role of lipid transfer proteins in allergic diseases,” Current Allergy and Asthma Reports, vol. 10, no. 5, pp. 326–335, 2010.
- A. E. Flinterman, J. H. Akkerdaas, A. C. Knlsta, R. van Ree, and S. G. Pasmans, “Hazelnut allergy: from pollen-associated mild allergy to severe anaphylactic reactions,” Current Opinion in Allergy and Clinical Immunology, vol. 8, no. 3, pp. 261–265, 2008.
- M. Fernández-Rivas, E. González-Mancebo, R. Rodríguez-Pérez, et al., “Clinically relevant peach allergy is related to peach lipid transfer protein, Pru p 3, in the Spanish population,” Journal of Allergy and Clinical Immunology, vol. 112, pp. 789–795, 2003.
- E. Vassilopoulou, L. Zuidmeer, J. Akkerdaas et al., “Severe immediate allergic reactions to grapes: part of a lipid transfer protein-associated clinical syndrome,” International Archives of Allergy and Immunology, vol. 143, no. 2, pp. 92–102, 2007.
- R. Asero, G. Mistrello, and S. Amato, “Anaphylaxis caused by tomato lipid transfer protein,” European Annals of Allergy and Clinical Immunology, vol. 43, no. 4, pp. 125–126, 2011.
- E. A. Pastorello, C. Pompei, V. Pravettoni et al., “Lipid-transfer protein is the major maize allergen maintaining IgE-binding activity after cooking at 100°C, as demonstrated in anaphylactic patients and patients with positive double-blind, placebo-controlled food challenge results,” Journal of Allergy and Clinical Immunology, vol. 112, no. 4, pp. 775–783, 2003.
- A. Nemni, J. -P. Borges, P. Rouge, et al., “Barley’s lipid transfer protein: a new emerging allergen in pediatric anaphylaxis,” Pediatric Allergy and Immunology, vol. 24, pp. 410–411, 2013.
- A. Hofmann and A. W. Burks, “Pollen food syndrome: update on the allergens,” Current Allergy and Asthma Reports, vol. 8, no. 5, pp. 413–417, 2008.
- H. A. Sampson, “Food allergy—accurately identifying clinical reactivity,” Allergy, vol. 60, supplement 79, pp. 19–24, 2005.
- S. J. Maleki, O. Viquez, T. Jacks et al., “The major peanut allergen, Ara h 2, functions as a trypsin inhibitor, and roasting enhances this function,” Journal of Allergy and Clinical Immunology, vol. 112, no. 1, pp. 190–195, 2003.
- A. E. Flinterman, E. van Hoffen, C. F. D. Jager et al., “Children with peanut allergy recognize predominantly Ara h2 and Ara h6, which remains stable over time,” Clinical and Experimental Allergy, vol. 37, no. 8, pp. 1221–1228, 2007.