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BioMed Research International
Volume 2013 (2013), Article ID 170452, 5 pages
Peanut Sensitization Profiles in Italian Children and Adolescents with Specific IgE to Peanuts
1UO Pediatria, Dipartimento di Scienze Mediche e Chirurgiche, University of Bologna, Via Massarenti 11, 40138 Bologna, Italy
2Pediatric Department, Azienda Ospedaliera-Universitaria, Department of Clinical and Experimental Medicine, University of Parma, Via Gramsci 14, 43126 Parma, Italy
Received 3 May 2013; Revised 22 September 2013; Accepted 10 October 2013
Academic Editor: Robert Movérare
Copyright © 2013 Elisabetta Calamelli 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.
Peanuts are one of the most relevant foods implicated in IgE-mediated adverse reactions in pediatric population. This study aimed to evaluate the pattern of sensitization towards five peanut allergenic components (rAra h 1, 2, 3, 8 and 9) in a population of Italian children and adolescents with specific IgE (sIgE) to peanut. rAra h 9 was the main allergen implicated in peanut sensitization (58%), followed by rAra h 8 (35%), rAra h 2 (27%), rAra h 3 (23%) and rAra h 1 (12.5%). rAra h 1, 2, and 3 were the main allergenic components in young children: 8/13 (62%) between 2 and 5 years, 8/23 (35%) between 6 and 11 years, and 3/12 (25%) between 1 and 16 years. No differences were found among the levels of sIgE towards rAra h 1, 2, 3, and 9 in the three groups; in contrast, the levels of sIgE against rAra h 8 showed an increasing trend according to age. In conclusion rAra h 1, 2, and 3 were the prevalent sensitizing allergens during the first years of life in Italian patients with sIgE to peanuts (“genuine” allergy); in contrast rAra h 9 and 8 were mainly involved in school-age children and adolescents with pollen allergy (“secondary” sensitization).
Peanuts (Arachis hypogaea) are one of the most relevant foods implicated in IgE-mediated adverse reactions, due to the frequency and severity of clinical manifestations . Peanut allergy is estimated to affect from 0.5 up to 1.8% of children in western countries [2–7]. In the last decade, the component-resolved diagnosis (CRD) approach has allowed the identification of specific IgE (sIgE) to different allergenic components of peanuts [8, 9]. Until now, thirteen peanuts allergens have been recognized (Ara h 1–13) . Among them, the seed storage proteins (SSPs) Ara h 1, Ara h 2 and Ara h 3 are the major peanut allergens and are considered to be the markers of genuine IgE-mediated peanut allergy [11, 12]. On the other hand, Ara h 8, a Bet v 1 homologue, is a pathogenesis-related protein 10 (PR-10) implicated in mechanisms of cross sensitization between pollens and foods , and the nonspecific lipid transfer protein (nsLTP) Ara h 9 is an allergen prevalent in the Mediterranean area . The sensitization against different allergenic components can help to predict the possible severity of symptoms . Indeed, the SSPs allergens are heat stable and resistant to enzymatic digestion and are implicated in systemic and life-threatening reactions [16, 17]. Ara h 8 is considered a marker of cross-reactivity between inhalant and food allergens, is rapidly digested by gastric enzymes, and is implicated in mild local reactions, such as oral allergy syndrome (OAS) [13, 18]. The LTPs are relevant allergens in patients from the Mediterranean area and are often implicated not only in local symptoms, but also in severe systemic reactions . This study aimed to evaluate the pattern of specific IgE (sIgE) against these five main allergenic components of Arachis hypogaea in a population of Italian children and adolescents with documented peanut sensitization (sIgE > 1 kUA/L) and a clinical history of suspected peanut and/or tree nuts allergy.
2. Materials and Methods
2.1. Study Population
The study involved 48 children (30 males, 62%, and 18 females, 38%) with a median age of 8 years (range 2–16 years) referred to the Pediatric Allergology Unit of Bologna University from November 2011 until December 2012. Inclusion criteria were a clinical history of suspected peanut and/or tree nuts allergy and a level of sIgE against peanut ≥ 1 kUA/L (ImmunoCAP 1000 Thermo Fisher Scientific, Uppsala, Sweden). Symptoms suggestive of atopic dermatitis and food and or respiratory allergy (asthma and rhino-conjunctivitis) were investigated in all enrolled patients. Parental history of atopy and the age of onset of allergic diseases were asked for all patients and/or to their parents. Of the forty-eight patients recruited for this study, 24 (50%) followed an elimination diet for peanuts or had never eaten them and were classified as “avoiders.” The rest of them, who used to eat peanuts without adverse reactions were defined to be “tolerant.” This research was performed in accordance with the principles of the Declaration of Helsinki.
2.2. Determination of Specific IgE
Serum sIgE was detected by the means of the CAP system (ImmunoCAP 1000 Thermo Fisher Scientific, Uppsala, Sweden). The determination of sIgE against a panel of inhalant [pollen from grass (Phleum pratense and Cynodon dactylon), birch (Betula verucosa), hazel (Corylus avellana) and olive tree (Olea europea)] and food allergens (peanut and its components (rAra h 1, rAra h 2, rAra h 3, r Ara h 8, and rAra h 9), hazelnut, walnut, rice, wheat, soy and apple) was performed in all patients’ sera. Levels of serum sIgE greater than 0.35 kUA/L were considered positive.
2.3. Statistical Methods
Data were stored by means of customized databases. Statistical analyses were carried out by means of MedCalc statistical software (Version 12.5.0, MedCalc Software, Ostend, Belgium). The Chi-square test and nonparametrical tests were applied when appropriate. In particular, proportions were compared by Chi-square test; geometric mean levels of sIgE were compared by Mann-Whitney U-test. Probability () values of less than 0.05 were considered significant.
3. Results and Discussion
The clinical and serological characteristics of the study population are resumed in Table 1. rAra h 9 was the main allergen implicated in peanut sensitization (58%), followed by rAra h 8 (35%), rAra h 2 (27%), rAra h 3 (23%) and rAra h 1 (12.5%). Twenty-six patients (54%) were sensitized to only one of the five allergenic components and in two cases (4%) none of the five investigated allergens were implicated. Twenty-four out of the 48 patients (50%) used to avoid peanuts’ consumption and were defined as “avoiders.” Detailed clinical and laboratory features of the study population categorized in the two subgroups (tolerant/avoiders) are resumed in Table 1. Among the group avoiding peanuts, 20 had never eaten peanuts; on the other hand four of them had experienced adverse reactions after peanuts ingestion (two cases of anaphylaxis, one of generalized urticaria and in one case oral allergy syndrome). Moreover, patients avoiding peanuts showed an higher rate of sensitization towards rAra h 1 and rAra h 2 than the tolerant group (resp. 25% versus 0% for rAra h 1 and 42% versus 12% for rAra h 2; ). Furthermore, patients avoiding peanuts showed a higher level of sIgE against peanut extract (12.5 kUA/L versus 6.5 kUA/L) and rAra h 2 (7.5 kUA/L versus 2 kUA/L) than the tolerant ones (). As shown in Table 2, half of the children avoiding peanuts were sensitized to more than one peanut component, compared to the 33% of tolerant patients (not significant).
We grouped patients in three age categories (2–5 years old (), 6–11 years old () and 12–16 years old ()) to evaluate differences in their molecular profiles (Figure 1). The SSPs were the main allergenic components implicated in peanut sensitization during the preschool age: 8/13 (62%) between 2–5 years, 8/23 (35%) between 6 and 11 years and only 3 patients out of 12 (25%) between 12 and 16 years. In contrast, the Bet v 1 homologue rAra h 8 and the LTP rAra h 9 were prevalent in school children and adolescents. The analysis of the geometric means of sIgE levels showed no relevant differences in the three age groups concerning both the SSPs and the LTPs, whereas the levels of sIgE against rAra h 8 showed an increasing trend according to age (from 1 kUA/L in preschool children to 4 kUA/L until 13.5 kUA/L in adolescents).
Our results confirm the relevance of the LTP Ara h 9 (positive in 58% of our study population) as a major allergen in peanut sensitized subjects living in a country of the Mediterranean area . Comparable results were shown by Vereda et al., who investigated the sensitization profiles of Spanish children and adolescents with peanut allergy . Meanwhile, Spanish patients showed a lower percentage of sensitization towards Ara h 8 (only 2% versus 35% in our study population) and Bet v 1 (6.5% versus 37% among our patients). These data reflect the lower birch pollen exposure among Spanish children and adolescents, compared to subjects from our geographical region (north of Italy). Indeed, the vegetation and plant distribution across the European countries shows relevant geographical differences from the northern to the southern regions, with a strong impact on the sensitization profiles of the living population . As shown from the Italian observational survey “Pan-allergens in Pediatrics,” children living in the Northern Italy have peculiar pattern of sensitization against plant-derived allergens (e.g., grasses, birch, hazel tree, and peanut) which differs from the population of the South of the peninsula . Interestingly, although in Italy the population mean of daily intake of peanuts is low (0.05 g/day versus 0.19 g/day in Europe), we found a relevant percentage of patients with peanut genuine sensitization (40% of our patients are sensitized to at least one of the SSPs), and most of them were small children . Unfortunately, no data are available about the peanuts’ daily intake in our study population, nor about the maternal consumption during pregnancy. Half of our children avoiding peanuts were sensitized to more than one peanut component, compared to the 33% of tolerant patients. Despite the fact that no significant differences were found between the two groups, our data are supported by previous researches, which highlighted more severe reactions in peanut allergic patients recognizing a greater number of allergens [23, 24].
Interestingly, our data showed an age-dependent sensitization pattern in patients with sIgE against peanut extract. Pre-school children were mostly sensitized (62%) to one of the SSPs peanuts allergens. In contrast, the Bet v 1 homologue Ara h 8 and the LTP Ara h 9 were prevalent in school children and adolescents, with levels of sIgE against Ara h 8 increasing with age. Since the sensitization to one of the peanuts’ SSPs (in particular Ara h 2) has been proved to be a marker of positive oral provocation test in patients with suspected peanut allergy, our findings show a possible more relevant risk of clinical reactions in patients with early onset of peanut sensitization .
The methodological limitations of this research need to be mentioned. Indeed, although the component-resolved diagnosis approach showed a detailed picture of the molecules implicated in the mechanism of peanut sensitization, the lack of complementary diagnostic tests (e.g., skin prick test, oral provocation test, and metabolite evaluation) is a bias of this study . In particular, the oral provocation test performed with peanuts might have better ascertained the tolerance status of those patients who had never eaten peanuts.
Despite these limitations, our data highlight the need for further research focusing on this phenomenon.
In conclusion, in our study the LTP rAra h 9 was the main implicated allergen in Italian patients with sIgE to peanuts, with similar prevalence in tolerant patients and patients avoiding peanuts. Moreover, both rAra h 9 and rAra h 8 were mainly involved in peanut sensitization in school age children and adolescents, with sIgE levels increasing with age, probably due to mechanism of cross-reactivity (secondary sensitization) in patients with pollen allergy. In contrast, the SSPs, in particular Ara h 1 and Ara h 2, were the prevalent sensitizing allergenic components in peanut avoiders, and their rates of sensitization were higher in preschool children, showing a phenomenon of genuine IgE-specific sensitization. Further research is needed to prove the clinical implications of these data.
- S. A. Bock, A. Muñoz-Furlong, and H. A. Sampson, “Further fatalities caused by anaphylactic reactions to food, 2001–2006,” Journal of Allergy and Clinical Immunology, vol. 119, no. 4, pp. 1016–1018, 2007.
- S. H. Sicherer, A. Muñoz-Furlong, and H. A. Sampson, “Prevalence of peanut and tree nut allergy in the United States determined by means of a random digit dial telephone survey: A 5-year Follow-Up Study,” Journal of Allergy and Clinical Immunology, vol. 112, no. 6, pp. 1203–1207, 2003.
- J. O. Hourihane, R. Aiken, R. Briggs et al., “The impact of government advice to pregnant mothers regarding peanut avoidance on the prevalence of peanut allergy in United Kingdom children at school entry,” Journal of Allergy and Clinical Immunology, vol. 119, no. 5, pp. 1197–1202, 2007.
- S. M. Tariq, M. Stevens, S. Matthews, S. Ridout, R. Twiselton, and D. W. Hide, “Cohort study of peanut and tree nut sensitisation by age of 4 years,” British Medical Journal, vol. 313, no. 7056, pp. 514–517, 1996.
- M. Morisset, D. A. Moneret-Vautrin, and G. Kanny, “Prevalence of peanut sensitization in a population of 4,737 subjects—an Allergo-Vigilance Network enquiry carried out in 2002,” European Annals of Allergy and Clinical Immunology, vol. 37, no. 2, pp. 54–57, 2005.
- J. Grundy, S. Matthews, B. Bateman, T. Dean, and S. H. Arshad, “Rising prevalence of allergy to peanut in children: data from 2 sequential cohorts,” Journal of Allergy and Clinical Immunology, vol. 110, no. 5, pp. 784–789, 2002.
- M. Osterballe, T. K. Hansen, C. G. Mortz, A. Høst, and C. Bindslev-Jensen, “The prevalence of food hypersensitivity in an unselected population of children and adults,” Pediatric Allergy and Immunology, vol. 16, no. 7, pp. 567–573, 2005.
- J. Sastre, “Molecular diagnosis in allergy,” Clinical and Experimental Allergy, vol. 40, no. 10, pp. 1442–1460, 2010.
- O. D. Wolthers, “Component-resolved diagnosis in pediatrics,” ISRN Pediatrics, vol. 2012, Article ID 806920, 6 pages, 2012.
- Allergen, 2013, http://www.allergen.org/.
- A. E. Flinterman, E. Van Hoffen, C. F. Den Hartog 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.
- M. Bublin, M. Kostadinova, C. Radauer et al., “IgE cross-reactivity between the major peanut allergen Ara h 2 and the nonhomologous allergens Ara h 1 and Ara h 3.,” The Journal of Allergy and Clinical Immunology, vol. 132, no. 1, pp. 118–124, 2013.
- 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.
- 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.
- R. Movérare, S. Ahlstedt, U. Bengtsson et al., “Evaluation of IgE antibodies to recombinant peanut allergens in patients with reported reactions to peanut,” International Archives of Allergy and Immunology, vol. 156, no. 3, pp. 282–290, 2011.
- X. Hong, D. Caruso, R. Kumar et al., “IgE, but not IgG4, antibodies to Ara h 2 distinguish peanut allergy from asymptomatic peanut sensitization,” Allergy, vol. 67, no. 12, pp. 1538–1546, 2012.
- W. C. Chiang, L. Pons, M. I. Kidon, W. K. Liew, A. Goh, and A. Wesley Burks, “Serological and clinical characteristics of children with peanut sensitization in an Asian community,” Pediatric Allergy and Immunology, vol. 21, no. 2, pp. e429–e438, 2010.
- A. Asarnoj, C. Nilsson, J. Lidholm, S. Glaumann, E. Östblom, and G. Hedlin, “Peanut component Ara h 8 sensitization and tolerance to peanut,” The Journal of Allergy and Clinical Immunology, vol. 130, no. 2, pp. 468–472, 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.
- G. D'Amato, L. Cecchi, S. Bonini et al., “Allergenic pollen and pollen allergy in Europe,” Allergy, vol. 62, no. 9, pp. 976–990, 2007.
- A. Dondi, S. Tripodi, V. Panetta, et al., “Pollen-induced allergic rhinitis in 1360 Italian children: comorbidities and determinants of severity,” Pediatric Allergy and Immunology. In press.
- M. Jenab, J. Sabaté, N. Slimani et al., “Consumption and portion sizes of tree nuts, peanuts and seeds in the European prospective investigation into cancer and nutrition (EPIC) cohorts from 10 European countries,” British Journal of Nutrition, vol. 96, no. 2, pp. S12–S23, 2006.
- K. A. B. M. Peeters, S. J. Koppelman, E. Van Hoffen et al., “Does skin prick test reactivity to purified allergens correlate with clinical severity of peanut allergy?” Clinical and Experimental Allergy, vol. 37, no. 1, pp. 108–115, 2007.
- S. A. Lewis, K. E. C. Grimshaw, J. O. Warner, and J. O. Hourihane, “The promiscuity of immunoglobulin E binding to peanut allergens, as determined by Western blotting, correlates with the severity of clinical symptoms,” Clinical and Experimental Allergy, vol. 35, no. 6, pp. 767–773, 2005.
- E. Eller and C. Bindslev-Jensen, “Clinical value of component-resolved diagnostics in peanut-allergic patients,” Allergy, vol. 68, no. 2, pp. 190–194, 2013.
- K. A. B. M. Peeters, R. J. A. N. Lamers, A. H. Penninks et al., “A search for biomarkers as diagnostic tools for food allergy: A Pilot Study in Peanut-Allergic Patients,” International Archives of Allergy and Immunology, vol. 155, no. 1, pp. 23–30, 2011.