Allergen Description
The following allergens have been characterised:
- Pru av 1, an 18 kDa protein, a Bet v 1-homologue, a major allergen. (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17)
- Pru av 2, a 23.3 to 29 kDa thaumatin-like protein. (2, 18, 19, 20, 21, 22)
- Pru av 3, a 15 kDa lipid transfer protein. (2, 4, 6, 7, 11, 13, 23, 24, 25, 26, 27)
- Pru av 4, a 15 kDa profilin. (2, 4, 6, 7, 11, 13, 28, 29, 30)
A beta-glucosidase (68 kDa) was isolated from ripe fruits of sweet cherry. (31) (Its allergenicity was not assessed, but beta-glucosidase is an allergen in other fruit.)
Pru av 1 was previously known as Pru a 1.
A heterogeneous sensitisation to cherry allergens occurs, and is influenced by geographic location. For example, Pru av 3, an LTP, has been identified as a major allergen in Mediterranean patients allergic to cherry, but was shown to be of minor clinical relevance in central and northern Europe, where birch trees are abundant. Patients with birch pollen-related cherry allergy are predominantly sensitised to the Bet v 1-homologous allergen Pru av 1. (7, 13, 16) Nonspecific LTPs are predominantly Rosaceae fruit allergens in the Mediterranean population, and sensitisation to these allergens occurs independently from allergy to birch pollen. Whereas symptoms to pollen-related food allergens in fruits typically cause only oral allergy syndrome (OAS), symptoms (in addition to OAS) of LTP-sensitised subjects are frequently systemic, including anaphylactic reactions. IgE reactivity to pollen-related food allergens is a consequence of primary sensitisation to inhalant allergens (commonly birch pollen), and of IgE cross-reactivity with homologous food allergens. In contrast, LTPs are probably capable of sensitising by the ingestion route. (7)
In a study of 101 cherry-allergic German and Italian patients, IgE prevalence was as follows: LTP (Pru av 3), 3 of 101 (3%); rPru av 1, 97 of 101 (96.0%); rPru av 4, 16 of 101 (16.2%); and cherry extract, 98 of 101 (97%). All 7 Italian patients had IgE against the cherry LTP. (13) In a study evaluating a panel of recombinant allergens for use in component-resolved in vivo diagnosis, with cherry as a model food, 79 subjects were included in the study: 24 Swiss patients (group 1) with a positive double-blind placebo-controlled food challenge result to cherry; 23 Swiss patients with birch pollen allergy but without cherry allergy (group 2); 23 non-atopic Swiss subjects (group 3); and 9 Spanish patients with a history of cherry allergy (group 4). SPT responses with rPru av 1, rPru av 4, and rPru av 3 were positive in 92%, 17%, and 4%, respectively, of the patients in group 1; in 74%, 30%, and 0% of the patients in group 2; in 0%, 22%, and 89% of the patients in group 4; and negative for all non-atopic subjects (group 3). (11)
In a study of 186 cherry-allergic subjects from central Europe and Spain, serum IgE was analysed with serum IgE tests carrying rPru av 1, 3 and 4, combined and separately, and cherry extract. Consistent with previous reports, major geographic differences in sensitisation patterns and prevalence of systemic reactions were found. A significantly higher rate of systemic reactions was found in Spanish patients sensitised to Pru av 3, whereas German patients sensitised to LTP had only oral allergy syndrome. (4)
Cherry Pru av 2, a thaumatin-like protein, is the most abundant soluble protein in ripe cherry; accumulation of this protein begins at the onset of ripening as the fruit turns from yellow to red. (22) Pru av 2 was recognised by the majority of cherry-allergic patients in a study, binding IgE of 50% of cherry-allergic patients. (18)
Cherry LTP Pru av 3 has been shown to have a high degree of resistance to digestion, and immunologically active Pru av 3 was detectable after 2 hours of digestion by pepsin, whereas IgE reactivity of Pru av 1 and Pru av 4 was eliminated within less than 60 minutes. Pru av 3 is also heat-stable. (7) There were no marked differences between the LTP of 6 cherry cultivars. LTP is found mainly in the peel, and chemical peeling has been shown to successfully remove Pru av 3. (23)
Cross Reactivity
Extensive cross-reactivity among the different individual species of the family could be expected. (26, 32)
Like other Prunus fruits, cherry contains a variety of allergenic proteins, including 2 birch tree pollen-homologous allergens, Bet v 1 and Bet v 2 (a profilin). Both Bet v 1 homologues and profilin may result in mild symptoms such as oral allergy syndrome, although sensitisation to profilin is commonly associated with more generalised symptoms, in particular urticaria and angioedema. (33) Lipid transfer protein may also be responsible for OAS in patients without pollen allergy, (23, 26) though adverse reactions are typically more severe. This is exemplified by a study of 14 subjects with Pru av 3 (LTP) sensitisation experiencing OAS, which was associated in some of the patients with gastrointestinal, respiratory or cardio-vascular symptoms. (7)
The relationship between pollen allergy and OAS to fruits and vegetables was evaluated in Sapporo, Japan, and it was found that out of 843 patients with birch-pollen allergy, 378 (37%) had episodes of OAS. The most frequent foods causing OAS were apple, peach and cherry, followed by kiwi, pear, plum and melon. (34) In an earlier study of 87 patients, in 61% of patients with birch allergy, apple (97%) was the most prevalent allergen resulting in OAS, followed by peach (67%), cherry (58%), pear (40%), plum (40%) and melon (33%). (35) In a European study, hazelnut (53%) was shown to be the most common food allergen associated with OAS in 380 birch pollen-allergic patients. Approximately 33% of these patients were also hypersensitive to almond and cherry, as reported on questionnaires. (36)
Pru av 1, a Bet v 1-homologous panallergen, has a 67% homology to Bet v 1. (15, 16) Cloned cherry allergen has a 59.1% identity to Bet v 1. (16) Some authors have described Pru av 1 as nearly identical with Bet v 1. (9, 17) This cross-reactive panallergen is found in (among other substances) cherry (Pru a 1), apple (Mal d 1), pear (Pyr c 1), celery (Api g 1), peach (Pru p 1) and carrot (Dau c 1). (15, 33, 37) Bet v 1 homologues mainly cause mild symptoms such as oral allergy syndrome (OAS). (33) Other Bet v 1 homologues are found in soya bean (Gly m 4) and peanut (Ara h 8). (38)
Pru av 2, a thaumatin-like protein (TLP), is a panallergen found in cherry and other foods. The amino acid sequence of cherry TLP has been shown to be highly homologous to grape and apple thaumatins. (39)
Pru av 3, a lipid transfer protein (LTP), is found in cherry. Pru av 3 shows high amino acid sequence identity with LTPs from peach (Pru p 3, 88%), apricot (Pru ar 3, 86%), and maize (Zea m 14, 59%), and no IgE cross-reactivity with birch pollen. (13) LTPs have also been shown to be present in walnut and peanut, (40) mugwort and chestnut, (41, 42) Vit v 1 from grape, (43) Cor a 8 from hazelnut, (44) Mal d 3 from apple, (45, 46) and Lac s 1 from lettuce. (47) Vit v 1, the LTP from grape, was shown to completely inhibit cherry LTP Pru av 3. (25) Hazelnut LTP has an amino acid identity of 59% with cherry LTP. (24) LTPs are also found in blueberry, raspberry, hazelnut, barley, asparagus, and carrot. (48) However, there is no firm correlation between sequence identity and clinical cross-reactivity, and therefore the degree of cross-reactivity resulting from LTPs varies among foods containing this panallergen. (47, 49) Lipid transfer proteins of Rosaceae fruits, including cherry, represent major allergens for atopic Mediterranean populations. (50)
Pru av 4, a profilin and panallergen, is recognised in about 20% of pollen-allergic patients from central Europe. However, sensitisation depends on the geographic area: in Swedish and Finnish patients, approximately 5-7% are sensitised to birch profilin, compared to 20-38% in central and southern Europe. (51) Approximately 20% of Spanish patients allergic to Bermuda grass were found to be sensitised to profilin, and about 42% of celery-allergic individuals to celery-profilin. (51) Sensitisation to profilin may result in cross-reactivity between cherry and other profilin-containing foods; although the cross-reactivity is quite variable, especially as profilin is heat-labile. Other foods containing profilin include tomato (Lyc e 1), celery (Api g 4), pineapple (Ana c 1), banana (Mus xp 1), carrot (Dau c 4) and pear (Pyr c 4). (28, 29, 52)
Pear (Pyr c 4) and Pru av 4 from cherry showed high amino acid sequence identity with birch pollen profilin, Bet v 2 (76-83%). Forty-three of 49 patients (88%) preselected for an IgE reactivity with Bet v 2 showed specific IgE antibodies to recombinant pear profilin, 92% to recombinant cherry profilin, and 80% to celery profilin. Profilins of peanut, cherry, pear, celery and birch have been shown to have marked differences in their IgE binding capacity. (30) IgE binding profiles indicate the presence of epitope differences among the related profilins, suggesting that cross-reactivity among related profilins may explain pollen-related allergy to food in a minority of patients. (28)
In a study of 61 patients with a documented history of IgE-mediated reactions to grapes or their products (wine, juice, and wine vinegar), 81.9% were co-sensitised to apple, 70.5% to peach, 47.5% to cherry, 32.8% to strawberry, 49.2% to peanut, 42.6% to walnut, 31.1% to hazelnut, 26.2% to almond, and 29.5% to pistachio. The high prevalence of concomitant reactivity to other fruits elicits an interest in the clinical relevance of these findings for the grape-allergic population. (53) In 11 Greek patients studied for IgE-mediated reactions to grapes, wine, or other grape products, other foods that induced anaphylaxis were apple (54.5%), cherry (18.6%), peach (18.6%), and banana (9.3%). Panallergens were not tested for. (54)