clear search
Search
Search Suggestions
Recent searches Clear History
Contact Us
Allergen Encyclopedia
Table of Contents

Whole Allergen

f96 Avocado

f96 Avocado Scientific Information

Type:

Whole Allergen

Display Name:

Avocado

Family:

Lauraceae

Latin Name:

Persea americana

Other Names:

Avocado, Alligator pear, Midshipman’s butter, Vegetable butter, Butter pear

Route of Exposure

Allergen Exposure

The Avocado originated in Central and South America and spread to nearly all parts of the tropical and subtropical world with suitable environmental conditions. Among leading producers are the larger islands of the Caribbean, California, New Zealand, the Philippines, Australia, South Africa and several Mediterranean countries. It belongs to the Lauraceae family, together with Cinnamon and Laurel. There are many varieties of Avocado. Two of the most common are Hass avocado (dark-coloured, wrinkled skin) and Strong avocado (green, smooth skin).

The Avocado tree may be 18 m tall or more. It is almost evergreen, with dark-green, glossy leaves. The fruit is pear-shaped, oval, or nearly round, and up to 33 cm long and 15 cm wide. The skin varies from yellow-green to almost black according to which variety the fruit belongs to. Generally, the flesh is pale to rich yellow, buttery, and bland or nutlike in flavour.

Avocados can be diced into salads, added to soups, stews, chili or omelettes, stuffed or garnished (with other vegetables, seafood, or mayonnaise or other dressings), or mashed to make guacamole (a blend of the pureed flesh with Lemon or Lime juice, Onion juice or powder, minced Garlic, Chili powder or Tabasco sauce, and salt and pepper) or sandwich spreads or dressings. In some cultures Avocados are treated more as a fruits and used in desserts. But they are less versatile than many fruits and vegetables, as they cannot be frozen or cooked, and their rapid discoloration when exposed to air necessitates that they be added to dishes at the last minute or kept fresh with Lemon juice or other preservatives. The oil is sometimes extracted for food uses and the pulp saved for stock feed.

The fruit are a good source of vitamins and minerals, having twice the potassium content of Bananas. Avocados are high in monosaturates. The oil content is second only to that of Olives among fruits, and sometimes greater. Clinical studies in humans have shown that Avocado oil can reduce blood cholesterol.

The oil is used as hair-dressing and as an ingredient in facial creams, hand lotions and fine soap. It is said to filter out the tanning rays of the sun, and is similar to lanolin in its penetrating and skin-softening action.

The seed and the roots contain an antibiotic that prevents bacterial spoilage of food and is the subject of 2 United States patents.
The skin and leaf juice are antibiotic. Among other uses, they are a treatment for worms, dysentery, pyorrhoea, wounds, diarrhoea, sore throat, toothache, skin eruptions and haemorrhage. Other functions include the stimulation and regulation of menstruation and the induction of abortion.

After 6 weeks, Avocado/Soybean unsaponi-fiables reduced the need for NSAID in patients with lower limb osteoarthritis (1).

Clinical Relevance

Allergen Description

Several antigenic constituents between 10 and 120 kDa have been revealed by immunoblotting studies (2-3). Sera of 11 patients were used to characterise allergens in Kiwi fruit, Latex, Avocado, and Banana and to identify cross-reactions among these allergen extracts. In Avocado extract, IgE-binding components of 27, 43, 52, 58, 65, 75, and 88 kDa were seen. Immunoblot inhibition demonstrated that almost all IgE-reactive bands in Latex, Avocado, and Banana extracts and 2 components of 43 and 67 kDa in Kiwi fruit shared common IgE epitopes (4).

The following allergens have been characterised:

  • Pers a 1, a class 1 chitinase, also known as a hevein-like protein (5-12). 
  • Pers a 4, a profilin (13). 
  • Pers a hevein (11).

Pers a 1, the major Avocado allergen, is a class I chitinase. It is a 32 kDa heat-labile protein. In a study, Pers a 1 induced positive skin reactivity responses in 7 of 8 patients with Latex-fruit allergy (5,7-8); and in a another study, it was recognised by 15 out of 20 Avocado- and/or Latex-allergic patients (9).

Pers a 1, a class I chitinase, is the panallergen involved in Latex-fruit syndrome. This substance was shown to be extensively degraded when subjected to simulated gastric fluid digestion, but the resulting peptides, particularly those corresponding to the hevein-like domain, were clearly reactive both in vitro and in vivo (10).

Potential Cross Reactivity

An extensive cross-reactivity among the different individual species of the genus could be expected but has not been documented yet (14).
Natural rubber latex IgE-mediated hyper-sensitivity is probably among the greatest challenges in the treatment of allergies during recent years. Some Latex allergens cross-react with plant-derived food allergens, and this has been termed the “Latex-fruit syndrome” (15). Almost 50% of the Latex-sensitised children have food allergies, mostly to Banana, Kiwi and Avocado (16).

Avocado contains a class I chitinase, a defense-related plant protein, and this panallergen results in extensive cross-reactivity with foods from different food families, including Green bean (6,17-18). The class I chitinase cross-reacts with a major Latex allergen, hevein, and is responsible for the syndrome (19-21). Hevein (Hev b 6.02 and Hev b 6.01) has elsewhere been reported to be the major cross-reacting allergen with Avocado in subjects with Latex allergy (8, 22-23). Sequence comparison has shown that Pers a 1 and prohevein had 70% similarity in their chitin-binding domains (9). This was confirmed by a study of Banana, Avocado, and Chestnut, which demonstrated a 65-70% sequence identity with the Latex hevein (24). Highly related 25 kDa class II chitinases lack the hevein-like domain, and in Avocado no IgE-binding capacity was shown by these class II enzymes (25). Skin prick test reactivities against purified proteins were examined in 15 patients with Natural rubber latex allergy. Eleven (73%) patients had skin prick test reactions to isolated hevein-like domains of Avocado and Banana, but only 1 (7%) patient reacted to their corresponding 31 kDa endochitinases. A hevein-like domain from Avocado and one from Banana inhibited binding of IgE to prohevein (Hev b 6.01) in 59% and 38% of patients, respectively, whereas corresponding percentages for 31 kDa endochitinases were 17% and 20%, respectively. The study concluded that the isolated hevein-like domain molecules alone, but not when linked to endochitinases, seem to be responsible for IgE-mediated clinical reactions in Latex-fruit syndrome. Isolated hevein-like domains, but not 31 kDa endochitinases, are responsible for IgE-mediated in vitro and in vivo reactions in Latex-fruit syndrome (11).

Hevein has also been implicated in the cross-reactivity seen between Avocado, Custard apple and Aubergine. Purified Hev b 6.02 and Pers a 1 induced positive responses in skin prick tests (12).

The Hevea brasiliensis Latex chitinase, designated Hev b 11, displays 70% identity to the endochitinase from Avocado, and its hevein domain displays 58% identity to hevein (Hev b 6.02). A study concluded that Hev b 11, a class I chitinase, is another allergen from Hevea Latex with a chitin binding domain, but that it displays a different IgE binding capacity, compared with hevein (26). A recombinant Hev b 11.0102 class I chitinase from Natural rubber latex plant leaves was reported to represent an allergen of intermediate prevalence in NRL, and cross-reactivity with certain fruits was suggested (27).

Considerable immunologic cross-reactivity between Natural rubber latex and Avocado has been reported. In a study, sera from 18 patients with previously verified Latex allergy were used as the source of IgE antibodies, and 11 of the patients underwent SPT with fresh Avocado. Fourteen of the 18 sera (78%) had IgE antibodies that bound to a total of 17 Avocado proteins with apparent molecular weights ranging from 16 to 91 kDa. The 10 most strongly reacting sera were used for immunoblot inhibition studies. Binding of IgE antibodies to solid-phase Avocado proteins was inhibited in a dose-dependent manner: 100 micrograms of NRL proteins inhibited IgE binding to 15 of the 17 Avocado proteins, and 10 micrograms caused inhibition to 13 protein bands. Skin reactivity to fresh Avocado was detected in 7 of the 11 patients with Latex allergy. The study reported that the large number of inhibitable proteins in immunoblot experiments, and clinical observations from skin prick tests suggest considerable immunologic cross-reactivity between NRL and Avocado. The study concluded that the observed cross-reacting protein components may be responsible for the recently reported type I hypersensitivity reactions to NRL and Avocado in patients with a pre-existing allergy to either allergen (3).
In a French study of 243 children attending an allergy out-patient unit during 1 year, the prevalence of Latex allergy was 1.3%. Avocado allergy was the food allergy most commonly associated with clinical symptoms (28).

A number of studies have reported cross-reactivity between Latex and a variety of foods, including Chestnut, Banana, Avocado, Passion fruit, Celery, Potato, Tomato, Kiwi and Peach (29-34).

An increasing number of plant sources, such as Avocado, Banana, Chestnut, Kiwi, Peach, Tomato, Potato and Bell pepper, have been associated with the Latex-fruit syndrome (35). Although in Latex-allergic patients multiple sensitisation to fruits may be observed, Banana and Avocado are the substances most frequently involved, followed by Chestnut and Melon (59). In 3 patients who developed anaphylactic reactions to both Latex and food, the food items that led to anaphylactic reactions were, for each patient, Banana and Avocado; Banana, Avocado and Buckwheat; and Banana, Avocado and Tomato (36).

Cross-reactivity with fruit in Latex-allergic patients has to be taken into account in evaluating and counseling, as it will be relevant for 60 to 70% of these individuals (37). Cross-reactivity may not be equal among the foods implicated. For example, in a study of 47 Latex-allergic patients, immunological reactivity to foods was found in 33. Seventeen patients manifested a clinical allergy to at least 1 food, including 11 cases of anaphylaxis, and 14 cases of local sensitivity reactions. Positive food skin reactivity was detected most frequently with Avocado (53%), Potato (40%), Banana (38%), Tomato (28%), Chestnut (28%), and Kiwi (17%). Cross-reactivity to Potato in Latex-allergic patients may result from a broad class of plant proteins known as patatins (38).

Hev b 7 is a Hevea brasiliensis Latex allergen with sequence identities of 39% to 42% to patatins. However, Hev b 7, patatins, and their homologues do not contribute to cross-reactivity in Latex-fruit syndrome (39).

Other studies have reported similar findings. In a study of cross-reactivity among 13 Latex-allergic individuals also allergic to food, the most frequent food hypersensitivities were to Avocado (n=9), Chestnut (n=9), Banana (n=7), Kiwi (n=5) and Papaya (n=3) (40). Similarly, in a study investigating the prevalence of Natural rubber latex sensitisation and allergy in children with atopic dermatitis, 12 of the 74 atopic children studied had circulating IgE antibodies to Latex. Of the specific food IgE evaluations, 18.4% (93 out of 505) were positive, and 69.9% were observed in the group of children with Latex-specific IgE antibodies; the evaluations were most frequently positive to Potato, Tomato, Sweet pepper, and Avocado. Twenty children without proven Latex sensitisation showed increased food-specific IgE antibodies, most frequently to Potato, Banana, and Chestnut (41).

Similarly, in 82 patients (43 men and 39 women, aged between 18 and 45 years) with Latex allergy, 39 (47.5%) were found to have positive SPT to fruit. SPT with fruit extracts was positive in 28 patients (Kiwi [n=21], Banana [n=17], Avocado [n=8], Papaya [n=3]); the prick-by-prick test showed a lower number of positive results (Kiwi [n=7], Banana [n=4], and Avocado [n=3]) (42).

In 137 patients with Latex allergy (with food allergy having been diagnosed by a convincing history of possible IgE-mediated symptoms occurring within 60 minutes of ingestion), 49 potential allergic reactions to foods were identified in 29 (21.1%) patients. Foods responsible for these reactions included Banana (n=9; 18.3%), Avocado (n=8; 16.3%), shellfish (n=6; 12.2%), fish (n=4; 8.1%), Kiwi (n=6; 12.2%), Tomato (n=3; 6.1%), Watermelon, Peach, Carrot (n=2; 4.1% each), and Apple, Chestnut, Cherry, Coconut, Apricot, Strawberry, and loquat, (n=1; 2.0% each). Reactions to foods included local mouth irritation, angioedema, urticaria, asthma, nausea, vomiting, diarrhoea, rhinitis, and anaphylaxis (43).

In a Latex allergy study, positive food-specific IgE antibody tests occurred most frequently with Avocado (53%), Potato (40%), Banana (38%), Tomato (28%), Chestnut (28%), and Kiwi (17%) (38).
The majority of studies document cross-reactivity between Latex allergy and Avocado, 1 among a number of cross-reactive foods, but not often between Avocado and other food. Nonetheless, these studies indicate that an Avocado-allergic individual is at risk of being allergic to a number of these foods because of the presence of the class I chitinase. Illustrating this, in a study of 17 serum samples from patients with well-documented Latex allergy, 10 demonstrated an allergy to Avocado, sometimes associated with Banana (2). In a study examining Banana allergy in 4 patients who were Banana-allergic, 1 patient also had a sensitisation to Avocado, but not to Latex or pollen (44).

However, Latex-allergic individuals may demonstrate IgE antibodies to these cross-reactive foods without clinical significance. For example, in a report of 2 children with Latex allergy, skin reactivity was detected for Banana, Kiwi, Pineapple, Apricot, Avocado, and Grape, but these children presented no symptoms after ingestion of these fruits (45). This finding is supported by a number of other studies. In a study of 136 patients with well-documented, clinically relevant, immediate-type hypersensitivity against Latex proteins, serum samples were analysed for IgE antibodies against a panel of different fruits. Cross-reacting IgE antibodies recognising Latex and fruit allergens (Papaya, Avocado, Banana, Chestnut, Passion fruit, Fig, Melon, Mango, Kiwi, Pineapple, Peach, and Tomato) were demonstrated by RAST-inhibition tests. Of the patients, 42.5% reported allergic symptoms after ingestion of these fruits, and a total of 112 intolerance reactions were recorded. However, fruit-specific IgE antibodies were detected in serum samples from only 32.1% of the patients who perceived symptoms due to these fruits. Therefore, serologic tests seem to be of low efficacy for prediction of food allergy in Latex-allergic patients (46). In 2 atopic Latex allergy patients with skin reactivity and IgE antibodies to Avocado and other fruit, no clinical symptoms occurred (47).

Cha o 2, a major allergen of Japanese cypress (Chamaecyparis obtuse) pollen, displays a high homology (a 74.3% identity) with Cry j 2, a major allergen of Japanese cedar (Cryptomeria japonica) pollen. This allergen is a polygalacturonase and showed a significant identity with a similar protein isolated in Avocado, Tomato, and Maize, as well as Cry j 2 (48). The deduced amino acid sequence of cloned Cry j II showed significant identities to those of the polygalacturonases associated with fruit ripening in Tomato (40%) and Avocado (43%) and also found in pollen of Maize (34%) (49). The allergenic potential of the Avocado-equivalent protein was not examined.

Allergy to other foods has been associated with Kiwi allergy: among Kiwi-allergic patients, there were strong reactions to Apple and Hazelnut; and moderate reactions to Carrot, Potato, and Avocado. A proposed mechanism was not suggested (50). Similarly, cross-reactivity among Apricot, Avocado, Banana, Cherry, Chestnut, Grape, Kiwi, Papaya, Passion fruit, Peach and Pineapple was reported (51).
In a study of 5 patients with oral allergy syndrome or anaphylaxis after the ingestion of Fig, and 1 patient with symptoms from exposure to Ficus benjamina trees (Weeping Fig), skin reactivity was demonstrated most often to Kiwi fruit, Papaya, and Avocado.

Sensitisation to Rubber latex could not be demonstrated in any of the patients. The study concluded that allergic reactions to fresh or dried Fig can present as a consequence of primary sensitisation to airborne Ficus benjamina allergens independent of sensitization to Rubber Latex allergens. Kiwi fruit, Papaya, and Avocado as well as Pineapple and Banana may be other fruits associated with sensitisation to Ficus allergens (52).

Among 4 patients with an allergy to Ficus benjamina, the 2 plant growers showed a cross-allergy to other Ficus species. Two patients had a cross-allergy to Latex and the associated cluster of tropical fruit (Banana, Kiwi, Avocado, and Chestnut) (53).

In a study that reported a sensitisation prevalence of 2.5% to Ficus benjamina Latex that occurred mostly independently of Latex allergy, sensitisation to F. benjamina was specifically associated with positive skin tests to fresh Fig (83%), dried Fig (37%), Kiwi fruit (28%), Papaya (22%), Avocado (19%), Banana (15%), and Pineapple (10%) (n = 54). The authors suggested that the cross-reactivity was mediated at least in part by the thiolproteases ficin and Papain (54).
In a study investigating the prevalence of Avocado allergy, 8 of 21 Avocado SPT positive patients reported that symptoms repeatedly followed the ingestion of Avocado; 7 also reported oral symptoms following Cantaloupe ingestion (55).

Molecular Aspects

Clinical Experience

IgE-mediated reactions

Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.

Avocado may commonly induce symptoms of food allergy in sensitised individuals (9,56-58), although the majority of reports describing allergy to Avocado do so in the context of cross-reactivity to Latex allergy (“Latex-fruit syndrome”) (11,42). The prevalence of Avocado allergy in the general population has been estimated to be around 1%, but this is increasing as consumption of Avocado dishes is increasing (9). Approximately 20% of atopic patients may have positive SPT to Avocado (55). Symptoms include local mouth irritation, angioedema, urticaria, abdominal pain, asthma, nausea, vomiting, diarrhoea, rhinoconjunctivitis, and anaphylaxis (31,43,55,59). Individuals experiencing itching in the mouth, diarrhoea, and/or swelling of the lips have been described (4). Oral allergy syndrome has also been reported (3,60).

In a study examining the prevalence of Avocado-induced symptoms, these were reported to occur in 8% of 100 consecutive atopic allergic rhinitis patients unselected for Avocado reactivity (55).

A study was conducted at 17 clinics in 15 European cities to evaluate the differences among some northern countries regarding what foods, according to food-allergic patients, elicit hypersensitivity symptoms. It was reported, after evaluation of questionnaires concerning 86 different foods, that the foods apparently most often eliciting symptoms in Russia, Estonia, and Lithuania were citrus fruits, chocolate, honey, Apple, Hazelnut, Strawberry, fish, Tomato, Hen’s egg, and Milk; these results differed from those of Sweden and Denmark, where Birch pollen-related foods, such as nuts, Apple, Pear, Kiwi, stone fruits, and Carrot, were the most common reported causes. The most common symptoms reported were oral allergy syndrome and urticaria. Birch pollen-related foods apparently dominated as allergens in Scandinavia, whereas some Mugwort-related foods seemed to be of more importance in Russia and the Baltic States. Among 1,139 individuals, Avocado was the 50th most reported food allergen, resulting in adverse effects in 9.0% (61).

In a study investigating the prevalence of Avocado allergy, 100 consecutive atopic patients with allergic rhinitis who underwent skin testing were also skin prick-tested to Avocado and/or tested for IgE antibodies to Avocado. Of the 100 atopic patients not selected for Avocado sensitivity, 21 had positive prick skin tests to Avocado. Eight of the 21 Avocado SPT-positive patients reported that symptoms repeatedly followed the ingestion of Avocado; 2 reported systemic reactions, but 6 noted oral symptoms only. Serum IgE antibodies to Avocado were elevated in 7 of the 8 patients reporting symptoms after eating Avocado (55).

In a study of 17 patients with immediate hypersensitivity to Avocado, systemic anaphylaxis occurred in 7, angioedema/urticaria in 6, vomiting in 2, asthma in 1, and rhinoconjunctivitis in 1. Skin prick tests with fresh Avocado were positive in all patients with the Strong avocado variety (SAv) and in 14 patients with the Hass avocado variety (HAv). Patient-associated sensitisations were as follows: 10 to Latex, 8 to Chestnut, 8 to Banana, 4 to Kiwi, and 4 to Walnut.

Avocado-sensitised patients with Latex allergy were typically middle-aged women, professionally exposed to Latex, who also exhibited frequent associated sensitisations to Chestnut, Banana, and other fruits. IgE antibodies against Avocado were demonstrated in 11 of the patients. The study reported that despite its lower protein content, SAv seems to be more allergenic than HAv, both in vivo and in vitro (40).
Food hypersensitivity is less frequent among adult patients than in childhood. In a study of 7,698 patients visiting an outpatient clinic, 120 reported consistent clinical symptoms after consumption of 1 or more foods: Shrimp (n=48), Squid (n=33), Kiwi (n=14), Papaya (n=14), Avocado (n=13) and Banana (n=12) were the most frequent causes of food hypersensitivity (62).

A 6-year-old boy was reported who presented with cutaneous and respiratory reactions to Banana and Avocado and from whom a history of adverse reactions to common Latex products was also elicited. IgE antibody test to Latex was strongly positive, equivocal to Avocado and Chestnut, and negative to Banana and Kiwi fruit, but the skin prick test was positive for Banana, Avocado and Chestnut (63). Other case reports indicate the variability of Avocado allergy; for example, a report was made of a Banana-allergic infant with IgE reactivity to Avocado but not to Latex (64).

Anaphylactic reaction to Avocado has been reported in a patient with pre-existing allergy to Natural rubber latex (65), and vice versa (66). In 2002, 107 cases were reported to the French Allergy Vigilance Network, of which 59.8 % were cases of anaphylactic shock, 18.7% systemic reactions, 15.9% laryngeal angioedema, and 5.6% serious acute asthma (including a fatality). Adults represented 69% of cases (74 cases). The most frequent causal allergens were Peanut, nuts, shellfish, and Latex group fruit (with 9 cases). The most frequent culprit foods for patients allergic to Latex were Avocado (n=4), Kiwi (n=2), Fig (n=2), and Banana (n=1) (67).

Contact urticaria from Latex in a patient with immediate hypersensitivity to Banana, Avocado and Peach was reported (68).
Reaction to Avocado oil in sunscreen has been documented (69-70).

Other reactions

Ingesting large amounts of Avocado may interfere with warfarin’s anti-clotting effects (71-72).

Vasoactive amines may result in allergy-like reactions.

Lactating livestock eating Avocado leaves may develop non-infectious mastitis and agalactia. The effects were attributed to an isolate, termed “persin,” found in Avocado leaves, which has been shown to have antifungal properties and to be toxic to silkworms (73). Other animals affected adversely are goats, horses and ostriches that have died of cardiomyopathy, heart failure and respiratory distress after eating Avocado leaves of Hass and Fuerte cultivars (74-75). Adverse effects have occurred in dogs that eat Avocado fruit (76). Dopamine has been found in the leaves. The leaf oil contains methyl chavicol. The seeds, ground and mixed with cheese or cornmeal, have been used to poison rodents.

Compiled By

Last reviewed: June 2022.

References
  1. Blotman F, Maheu E, Wulwik A, Caspard H,
    Lopez A. Efficacy and safety of avocado/soybean unsaponifiables in the treatment of symptomatic osteoarthritis of the knee and hip. A prospective, multicenter, three-month, randomized, double-blind, placebo-controlled trial. Rev Rhum Engl Ed 1997;64(12):825-34
  2. Lavaud F, Prevost A, Cossart C, Guerin L, Bernard J, Kochman S. Allergy to latex, avocado pear, and banana: Evidence for a 30 kd antigen in immunoblotting.
    J Allergy Clin Immunol 1995;95(2):557-64
  3. Ahlroth M, Alenius H, Turjanmaa K, Makinen-Kiljunen S, Reunala T, Palosuo T. Cross-reacting allergens in natural rubber latex and avocado.
    J Allergy Clin Immunol 1995;96(2):167-73
  4. Moller M, Kayma M, Vieluf D, Paschke A, Steinhart H. Determination and characterization of cross-reacting allergens in latex, avocado, banana, and kiwi fruit.
    Allergy 1998;53(3):289-96
  5. International Union of Immunological Societies Allergen Nomenclature: IUIS official list http://www.allergen.org/List.htm 2008
  6. Sánchez-Monge R, Blanco C, Perales AD, Collada C, Carrillo T, Aragoncillo C, Salcedo G. Class I chitinases, the panallergens responsible for the latex-fruit syndrome, are induced by ethylene treatment and inactivated by heating. J Allergy Clin Immunol 2000;106(1 Pt 1):190-5
  7. Breiteneder H, Ebner C. Molecular and biochemical classification of plant-derived food allergens. J Allergy Clin Immunol 2000;106(1 Pt 1):27-36
  8. Posch A, Wheeler CH, Chen Z, Flagge A, Dunn MJ, Papenfuss F, Raulf-Heimsoth M, Baur X.
    Class I endochitinase containing a hevein domain is the causative allergen in latex-associated avocado allergy.
    Clin Exp Allergy 1999;29(5):667-72
  9. Sowka S, Hsieh LS, Krebitz M, Akasawa A, Martin BM, Starrett D, Peterbauer CK,
    Scheiner O, Breiteneder H. Identification and cloning of Prs a 1, a 32-kDa endochitinase and major allergen of avocado, and its expression in the yeast Pichia pastoris.
    J Biol Chem 1998;273:28091-7
  10. Diaz-Perales A, Blanco C, Sanchez-Monge R, Varela J, Carrillo T, Salcedo G. Analysis of avocado allergen (Prs a 1) IgE-binding peptides generated by simulated gastric fluid digestion. J Allergy Clin Immunol 2003;112(5):1002-7
  11. Karisola P, Kotovuori A, Poikonen S, Niskanen E, Kalkkinen N, Turjanmaa K, Palosuo T, Reunala T, Alenius H, Kulomaa MS.
    Isolated hevein-like domains, but not 31-kd endochitinases, are responsible for IgE-mediated in vitro and in vivo reactions in latex-fruit syndrome.
    J Allergy Clin Immunol 2005;115(3):598-605
  12. Gamboa PM, Sanchez-Monge R, Diaz-Perales A, Salcedo G, Ansotegui J, Sanz ML. Latex-vegetable syndrome due to custard apple and aubergine: new variations of the hevein symphony. J Investig Allergol Clin Immunol 2005;15(4):308-11
  13. van Ree R, Voitenko V, van Leeuwen WA, Aalberse RC. Profilin is a cross-reactive allergen in pollen and vegetable foods.
    Int Arch Allergy Immunol 1992;98(2):97-104
  14. Yman L. Botanical relations and immunological cross-reactions in pollen allergy. 2nd ed. Pharmacia Diagnostics AB. Uppsala. Sweden. 1982: ISBN 91-970475-09
  15. Ikezawa Z, Osuna H. Latex-fruits syndrome. [Japanese] Arerugi 2002;51(8):591-604.
  16. Baker L, Hourihane J O’B. Latex allergy: Two educational cases.
    Pediatr Allergy Immunol 2008;19(6):477-81
  17. Salcedo G, Diaz-Perales A, Sanchez-Monge R. The role of plant panallergens in sensitization to natural rubber latex. Curr Opin Allergy Clin Immunol 2001;1(2):177-83
  18. Sanchez-Monge R, Blanco C, Diaz-Perales A, Collada C, Carrillo T, Aragoncillo C, Salcedo G.
    Isolation and characterization of major banana allergens: identification as fruit class I chitinases.
    Clin Exp Allergy 1999;29(5):673-80
  19. Blanco C. Latex-fruit syndrome.
    Curr Allergy Asthma Rep 2003;3(1):47-53
  20. Blanco Guerra C. Latex-fruit syndrome. [Spanish] Allergol Immunopathol (Madr) 2002;30(3):156-63
  21. Diaz-Perales A, Collada C, Blanco C, Sanchez-Monge R, Carrillo T, Aragoncillo C, Salcedo G. Cross-reactions in the latex-fruit syndrome: A relevant role of chitinases but not of complex asparagine-linked glycans. J Allergy Clin Immunol 1999;104(3 Pt 1):681-7
  22. Chen Z, Posch A, Cremer R, Raulf-Heimsoth M, Baur X. Identification of hevein (Hev b 6.02) in Hevea latex as a major cross-reacting allergen with avocado fruit in patients with latex allergy J Allergy Clin Immunol 1998;102(3):476-81
  23. Blanco C, Diaz-Perales A, Collada C, Sanchez-Monge R, Aragoncillo C, Castillo R, Ortega N, Alvarez M, Carrillo T, Salcedo G. Class I chitinases as potential panallergens involved in the latex-fruit syndrome. J Allergy Clin Immunol 1999;103(3 Pt 1):507-13
  24. Sanchez-Monge R, Diaz-Perales A, Blanco C, Salcedo G. Class I chitinases and the latex-fruit syndrome.
    Internet Symp Food Allergens 2000;2:137-44
  25. Diaz-Perales A, Collada C, Blanco C, Sanchez-Monge R, Carrillo T, Aragoncillo C, Salcedo G.
    Class I chitinases with hevein-like domain, but not class II enzymes, are relevant chestnut and avocado allergens.
    J Allergy Clin Immunol 1998;102(1):127-33
  26. O’Riordain G, Radauer C, Hoffmann-Sommergruber K, Adhami F, Peterbauer CK, Blanco C, Godnic-Cvar J, Scheiner O, Ebner C, Breiteneder H. Cloning and molecular characterization of the Hevea brasiliensis allergen Hev b 11, a class I chitinase. *Clin Exp Allergy 2002;32(3):455-62
  27. Rihs HP, Dumont B, Rozynek P, Lundberg M,
    Cremer R, Bruning T, Raulf-Heimsoth M. Molecular cloning, purification, and IgE-binding of a recombinant class I chitinase from Hevea brasiliensis leaves (rHev b 11.0102).
    Allergy 2003;58(3):246-51
  28. Mavale-Manuel S, Paty E, Scheinmann P, de Blic J. Latex allergy in children. [French] Arch Pediatr 2003;10(8):700-6
  29. Zaglaniczny K. Latex allergy: are you at risk? AANA J 2001;69(5):413-24
  30. Sanchez Palacios A. Latex allergy. Diagnosis and therapeutic aspects. [Spanish] Allergol Immunopathol (Madr) 2001;29(5):212-21
  31. Blanco C, Carrillo T, Castillo R, Quiralte J, Cuevas M. Avocado hypersensitivity.
    Allergy 1994;49:454-9
  32. Levy DA, Mounedji N, Noirot C, Leynadier F Allergic sensitization and clinical reactions to latex, food and pollen in adult patients.
    Clin Exp Allergy 2000;30(2):270-5
  33. Fujie S, Yagami A, Suzuki K, Akamatsu H, Matsunaga K. A case of the latex-induced anaphylaxis by contact with barium enema catheter. [Japanese] Arerugi 2004;53(1):38-42
  34. Ebo DG, Bridts CH, Hagendorens MM, De Clerck LS, Stevens WJ. The prevalence and diagnostic value of specific IgE antibodies to inhalant, animal and plant food, and ficus allergens in patients with natural rubber latex allergy. Acta Clin Belg 2003;58(3):183-9
  35. Wagner S, Breiteneder H. The latex-fruit syndrome.
    Biochem Soc Trans 2001;30(6):935-40
  36. Abeck D, Borries M, Kuwert C, Steinkraus V, Vieluf D, Ring J. Food-induced anaphylaxis in latex allergy. [German] Hautarzt 1994;45(6):364-7
  37. Heese A, Lacher U, Koch HU, Kubosch J, Ghane Y, Peters KP. Update on the latex allergy topic. [German] Hautarzt 1996;47(11):817-24
  38. Beezhold DH, Sussman GL, Liss GM, Chang NS.
    Latex allergy can induce clinical reactions to specific foods.
    Clin Exp Allergy 1996;26(4):416-22
  39. Sowka S, Hafner C, Radauer C, Focke M, Brehler R, Astwood JD, Arif SA, Kanani A, Sussman GL, Scheiner O, Beezhold DH, Breiteneder H. Molecular and immunologic characterization of new isoforms of the Hevea brasiliensis latex allergen hev b 7: evidence of no cross-reactivity between hev b 7 isoforms and potato patatin and proteins from avocado and banana.
    J Allergy Clin Immunol 1999;104(6):1302-10
  40. Blanco C, Carrillo T, Castillo R, Quiralte J, Cuevas M. Latex allergy: clinical features and cross-reactivity with fruits.
    Ann Allergy 1994;73(4):309-14
  41. Tucke J, Posch A, Baur X, Rieger C, Raulf-Heimsoth M Latex type I sensitization and allergy in children with atopic dermatitis. Evaluation of cross-reactivity to some foods Pediatr Allergy Immunol 1999;10(3):160-7
  42. Isola S, Ricciardi L, Saitta S, Fedele R, Mazzeo L, Fogliani O, Gangemi S, Purello-D’Ambrosio F. Latex allergy and fruit cross-reaction in subjects who are nonatopic.
    Allergy Asthma Proc 2003;24(3):193-7
  43. Kim KT, Hussain H. Prevalence of food allergy in 137 latex-allergic patients.
    Allergy Asthma Proc 1999;20(2):95-7
  44. Grob M, Reindl J, Vieths S, Wuthrich B, Ballmer-Weber BK. Heterogeneity of banana allergy: characterization of allergens in banana-allergic patients. Ann Allergy Asthma Immunol 2002;89(5):513-6
  45. Bernardini R, Novembere E, Brizzi I, Bertini G, Mariani E, Vierucci A. Latex allergy in children: description of two cases. [Italian] Pediatr Med Chir 1995;17(2):169-71
  46. Brehler R, Theissen U, Mohr C, Luger T.
    ”Latex-fruit syndrome”: frequency of cross-reacting IgE antibodies.
    Allergy 1997;52(4):404-10
  47. Monreal P, Server MT, Torrens I, Soler Escoda JM.
    Hipersensitivity to fruits in latex allergic patients. Allergol Immunopathol Madr 1996;24(1):33-5
  48. Mori T, Yokoyama M, Komiyama N, Okano M, Kino K. Purification, identification, and cDNA cloning of Cha o 2, the second major allergen of Japanese cypress pollen. Biochem Biophys Res Commun 1999;263(1):166-71
  49. Komiyama N, Sone T, Shimizu K, Morikubo K, Kino K. cDNA cloning and expression of
    Cry j II the second major allergen of Japanese cedar pollen. Biochem Biophys Res Commun 1994;201(2):1021-8
  50. Gall H, Kalevam KJ, Forck G, Sterry W. Kiwi fruit allergy: a new birch pollen-associated food allergy. J Allergy Clin Immunol 1994;94:70-6
  51. Twarog FJ. Food-induced allergy in childhood. Allergy Asthma Proc 1998;19(4):219-222
  52. Focke M, Hemmer W, Wohrl S, Gotz M, Jarisch R. Cross-reactivity between Ficus benjamina latex and fig fruit in patients with clinical fig allergy.
    Clin Exp Allergy 2003;33(7):971-7
  53. van Ginkel CJ, Dijkstra AT, van Eyk CL, den Hengst CW, Bruijnzeel-Koomen CA. Allergy to Ficus benjamina: at the workplace and at home. [Dutch] Ned Tijdschr Geneeskd 1997;141(16):782-4
  54. Hemmer W, Focke M, Gotz M, Jarisch R. Sensitization to Ficus benjamina: relationship to natural rubber latex allergy and identification of foods implicated in the Ficus-fruit syndrome. Clin Exp Allergy 2004;34(8):1251-8
  55. Telez-Diaz G, Ellis MH, Morales Russo F, Heiner DC. Prevalence of avocado allergy among atopic patients.
    Allergy Proc 1995;16(5):241-3
  56. Crespo JF, Rodriguez J, James JM, Daroca P, Reano M, Vives R. Reactivity to potential cross-reactive foods in fruit-allergic patients: implications for prescribing food avoidance. Allergy 2002;57(10):946-9
  57. Zuidmeer L, Goldhahn K, Rona RJ, Gislason D, Madsen C, Summers C, Sodergren E, Dahlstrom J, Lindner T, Sigurdardottir ST, McBride D, Keil T. The prevalence of plant food allergies: a systematic review.
    J Allergy Clin Immunol 2008;121(5):1210-8
  58. Rance F, Grandmottet X, Grandjean H. Prevalence and main characteristics of schoolchildren diagnosed with food allergies in France. Clin Exp Allergy 2005;35(2):167-72
  59. Latasa M, Diéguez I, Sanz ML, Parra A, Pajarón MJ, Oehling A. Fruit sensitization in patients with allergy to latex. J Investig Allergol Clin Immunol 1995;5(2):97-102
  60. Ortega N, Quiralte J, Blanco C, Castillo R, Alvarez MJ, Carrillo T. Tobacco allergy: demonstration of cross-reactivity with other members of Solanaceae family and mugwort pollen. Ann Allergy Asthma Immunol 1999;82(2):194-7
  61. Eriksson NE, Moller C, Werner S, Magnusson J, Bengtsson U, Zolubas M. Self-reported food hypersensitivity in Sweden, Denmark, Estonia, Lithuania, and Russia. J Investig Allergol Clin Immunol 2004;14(1):70-9
  62. Castillo R, Delgado J, Quiralte J, Blanco C, Carrillo T. Food hypersensitivity among adult patients: epidemiological and clinical aspects. Allergol Immunopathol Madr 1996;24(3):93-7
  63. Freeman GL. Cooccurrence of latex and fruit allergies. [Review] Allergy Asthma Proc 1997;18(2):85-8
  64. Ito A, Ito K, Morishita M, Sakamoto T.
    A banana-allergic infant with IgE reactivity to avocado, but not to latex.
    Pediatr Int 2006;48(3):321-3
  65. Lavaud F, Cossart C, Reiter V, Bernard J, Deltour G, Holmquist I. Latex allergy in patient with allergy to fruit. Lancet 1992;339:492-3
  66. Ceuppens JL, Van Durme P, Dooms-Goossens A.
    Latex allergy in patient with allergy to fruit. Lancet 1992;339(8791):493
  67. Moneret-Vautrin DA, Kanny G, Morisset M, Rance F, Fardeau MF, Beaudouin E. Severe food anaphylaxis: 107 cases registered in 2002 by the Allergy Vigilance Network.
    Allerg Immunol (Paris) 2004;36(2):46-51
  68. Crisi G, Belsito DV. Contact urticaria from latex in a patient with immediate hypersensitivity to banana, avocado and peach.
    Contact Dermatitis 1993;28(4):247-8
  69. de Groot AC, van der Meeren LM, Weyland JW. Contact allergy to avocado oil in a sunscreen Contact Dermatitis 1987;16(2):108-9
  70. Nater JP, De Groot AC. Unwanted effects of cosmetics and drugs used in dermatology. 2nd Ed. Amsterdam.
    Elsevier Science Publ 360-7, 425-5
  71. Wells PS, Holbrook AM, Crowther NR, Hirsh J. Interactions of warfarin with drugs and food. Ann Intern Med 1994;121(9):676-83
  72. Blickstein D, Shaklai M, Inbal A Warfarin antagonism by avocado.
    Lancet 1991;337(8746):914-5
  73. Oelrichs PB, Ng JC, Seawright AA, Ward A, Schaffeler L, MacLeod JK. Isolation and identification of a compound from avocado (Persea americana) leaves which causes necrosis of the acinar epithelium of the lactating mammary gland and the myocardium. Nat Toxins 1995;3(5):344-9
  74. Burger WP, Naude TW, Van Rensburg IB, Botha CJ, Pienaar AC Cardiomyopathy in ostriches (Struthio camelus) due to avocado (Persea americana var. guatemalensis) intoxication.
    J S Afr Vet Assoc 1994;65(3):113-8
  75. Grant R, Basson PA, Booker HH, Hofherr JB, Anthonissen M Cardiomyopathy caused by avocado (Persea americana Mill) leaves.
    J S Afr Vet Assoc 1991;62(1):21-2
  76. Buoro IB, Nyamwange SB, Chai D, Munyua SM.
    Putative avocado toxicity in two dogs. Onderstepoort J Vet Res 1994;61(1):107-9