f96 Avocado

Allergens within Food of Plant Origin

  • Latin name: Persea americana
  • Family: Lauraceae
  • Common names: Avocado
Varieties:
Guatemalan: Persea nubigena var. guatamalensis L. Wms.
Mexican: P. americana var. drymifolia Blake
West Indian: P. americana Mill. var. americana (P. gratissima Gaertn.)

Food
A food, which may result in allergy symptoms in sensitised individuals.

Allergen Exposure

Geographical distribution
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 15cm wide. The skin varies from yellow-green to almost black according to which of several varieties the fruit belongs to. Generally, the flesh is pale to rich-yellow, buttery, and bland or nutlike in flavour.
 
Environment
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 they 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 fruits 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 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 is employed in making 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 which prevents bacterial spoilage of food. It is the subject of two 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 six weeks, Avocado/Soybean unsaponifiables reduced the need for NSAID in patients with lower limb osteoarthritis (1). 
 
Unexpected exposure
Avocado oil may be added to cosmetics.
 
Allergens
Several antigenic constituents between 10 and 120 kDa have been revealed by immunoblotting studies (2-3).
 
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-specific responses in 7 of 8 patients with Latex-fruit allergy (4-6) and in a another study was recognised by 15 out of 20 Avocado- and/or Latex-allergic patients (7).
 
Pers a 1, is the panallergen involved in Latex-fruit syndrome. Pers a 1 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 (8).
 
In a study, 11 patients were used to characterise allergens in Kiwi fruit, Latex, Avocado, and Banana to determine cross-reactions between 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 (9).

Potential Cross-Reactivity

An extensive cross-reactivity among the different individual species of the genus could be expected but has not been documented yet (10).
 
Natural Rubber Latex immunoglobulin E-mediated hypersensitivity is probably one of 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” (11).
 
Avocado contains a class I chitinase, a defense-related plant protein, and this panallergen results in extensive cross-reactivity between foods from different food families, including Green bean (4, 12, 13). The class I chitinase cross-reacts with a major Latex allergen, hevein, and is responsible for the syndrome (14-16). Hevein (Hev b 6.02 and Hev b 6.01) has been reported to be the major cross-reacting allergen with Avocado in subjects with Latex allergy (6, 17, 18). Sequence comparison has shown that Prs a 1 and prohevein had 70% similarity in their chitin-binding domains (7). This was confirmed by a study of Banana, Avocado, and Chestnut, which demonstrated a 65-70% sequence identity with the Latex hevein (19). 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 (20). 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 and displays a different IgE binding capacity, compared with hevein (21). 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 a property of cross-reacting with certain fruits was suggested (22).
 
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 skin-specific IgE testing 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-specific IgE 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 suggests 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 (23).
 
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 (24-28).  
 
An increasing number of plant sources, such as Avocado, Banana, Chestnut, Kiwi, Peach, Tomato, Potato and Bell pepper, have been associated with this syndrome (29). 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 (50). 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 (30).
 
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 (31). 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-specific IgE was detected most frequently with Avocado (53%), Potato (40%), Banana (38%), Tomato (28%), Chestnut (28%), and Kiwi (17%). Cross-reactivity in Latex-allergic patients to Potato may be as a result of a broad class of plant proteins known as patatins (32). 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 the Latex-fruit syndrome (33).
 
Other studies have reported similar findings. In a study of cross-reactivity among 13 Latex-allergic individuals allergic to food, the most frequent food hypersensitivities were to Avocado (9), Chestnut (9), Banana (7), Kiwi (5) and Papaya (3, 34). 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; the evaluations were most frequently positive to Potato, Tomato, Sweet pepper, and Avocado. Twenty children without proven Latex sensitisation showed increased food-specific IgE, most frequently to Potato, Banana, and Chestnut (35).
 
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 skin-specific IgE to fruit. Skin-specific IgE determination with fruit extracts was positive in 28 patients (Kiwi (21), Banana (17), Avocado (8), Papaya (3)); the prick-by-prick test showed a lower number of positive results (Kiwi (7), Banana (4), and Avocado (3)) (36).
 
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 (9; 18.3%), Avocado (8;16.3%), shellfish (6; 12.2%), fish (4; 8.1%), Kiwi (6; 12.2%), Tomato (3; 6.1%), Watermelon, Peach, Carrot (2; 4.1% each), and Apple, Chestnut, Cherry, Coconut, Apricot, Strawberry, and loquat, (1; 2.0% each). Reactions to foods included local mouth irritation, angioedema, urticaria, asthma, nausea, vomiting, diarrhoea, rhinitis, and anaphylaxis (37).
 
In a Latex allergy study, positive food-specific IgE tests occurred most frequently with Avocado (53%), Potato (40%), Banana (38%), Tomato (28%), Chestnut (28%), and Kiwi (17%) (32).
 
The majority of studies document cross-reactivity between Latex allergy and Avocado, 1 among a number of cross-reactive foods, and 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. To demonstrate, 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 (38).
 
However, Latex-allergic individuals may demonstrate specific IgE to these cross-reactive foods without clinical significance. For example, in a report of 2 children with Latex allergy, skin-specific IgE was detected for Banana, Kiwi, Pineapple, Apricot, Avocado, and Grape, but these children presented no symptoms after ingestion of these fruits (39). 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 seemed to be of low significance for prediction of food allergy in Latex-allergic patients (40). In 2 atopic Latex allergy patients with skin- and serum-specific IgE to Avocado and other fruit, no clinical symptoms occurred (41).
 
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 (42). 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 found in pollen of Maize (34%) (43). The allergenic potential of the Avocado equivalent protein was not examined.
 
Allergy to other foods has been associated with Kiwi allergy: strong reactions to Apple and Hazelnut; and moderate reactions to Carrot, Potato, and Avocado. A proposed mechanism was not suggested (44). Similarly, cross-reactivity between Apricot, Avocado, Banana, Cherry, Chestnut, Grape, Kiwi, Papaya, Passion fruit, Peach and Pineapple was reported (45).
 
In a study of 5 patients with oral allergy syndrome or anaphylaxis after the ingestion of Figs, and 1 patient with symptoms from exposure to Ficus benjamina trees (Weeping Fig), skin-specific IgE 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 Figs can present as a consequence of primary sensitisation to airborne Ficus benjamina allergens independent of sensitisation 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 (46).
 
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) (47).
 
In a study investigating the prevalence of Avocado allergy, 8 of 21 Avocado skin-specific IgE positive patients reported that symptoms repeatedly followed the ingestion of Avocado; 7 also reported oral symptoms following Cantaloupe ingestion (48).

Clinical Experience

IgE-mediated reactions
Avocado may commonly induce symptoms of food allergy in sensitised individuals (7) (49) although the majority of reports describing allergy to Avocado do so in the context of cross-reactivity to Latex allergy ("latex-fruit syndrome") (36). 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 (7). Approximately 20% of atopic patients may test positive for the presence of skin specific IgE to Avocado (48). Symptoms include local mouth irritation, angioedema, urticaria, abdominal pain, asthma, nausea, vomiting, diarrhoea, rhinoconjunctivitis, and anaphylaxis (26, 37, 48, 50). Individuals experiencing itching in the mouth, diarrhoea, and/or swelling of the lips have been described (9). Oral allergy syndrome has also been reported (3, 51).
 
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 (48).
 
In a study investigating the prevalence of Avocado allergy, 100 consecutive atopic patients with allergic rhinitis undergoing skin testing were also skin prick tested to Avocado and/or tested for specific serum 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 skin test-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 (48).
 
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 test with fresh Avocado was 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. Specific IgE against Avocado was 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 (34).
 
Food hypersensitivity is less frequent among adult patients than in childhood. In a study of 7698 patients visiting an Outpatient Clinic, 120 patients reported consistent clinical symptoms after consumption of one or more foods: Shrimp (48), Squid (33), Kiwi (14), Papaya (14), Avocado (13) and Banana (12) were the most frequent causes of food hypersensitivity (52).
 
Anaphylactic reaction to avocado has been reported in a patient with pre-existing allergy to natural rubber latex (53) and vice versa (54).
 
Contact urticaria from Latex in a patient with immediate hypersensitivity to Banana, Avocado and Peach was reported (55).
 
Reaction to Avocado oil in sunscreen has been documented (56-57).
 
Other reactions
Ingesting large amounts of Avocado may interfere with warfarin's anti-clotting effects (58, 59).
 
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 (60). 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 (61-62). Adverse effects have occurred in dogs after eating Avocado fruit (63). 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 Dr Harris Steinman, harris@zingsolutions.com

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 Dec;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):557-564
    3. Ahlroth M, Alenius H, Turjanmaa K, Makinen Kiljunen S, et al. Cross-reacting allergens in natural rubber latex and avocado. J Allergy Clin Immunol 1995;96(2):167-73
    4. Sanchez-Monge R, Blanco C, Perales AD, Collada C, Carrillo T, et al. 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
    5. Breiteneder H, Ebner C. Molecular and biochemical classification of plant-derived food allergens. J Allergy Clin Immunol. 2000;106(1 Pt 1):27-36
    6. 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
    7. Sowka S, Hsieh LS, Krebitz M, et al. 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;273:28091-28097
    8. 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
    9. 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
    10. Yman L. Botanical relations and immunological cross-reactions in pollen allergy. 2nd ed. Pharmacia Diagnostics AB. Uppsala. Sweden. 1982: ISBN 91-970475-09
    11. Ikezawa Z, Osuna H. Latex-fruits syndrome. [Japanese] Arerugi 2002;51(8):591-604
    12. 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.
    13. 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
    14. Blanco C. Latex-fruit syndrome. Curr Allergy Asthma Rep 2003;3(1):47-53
    15. Blanco Guerra C. Latex-fruit syndrome. [Spanish] Allergol Immunopathol (Madr) 2002;30(3):156-63
    16. Diaz-Perales A, Collada C, Blanco C, Sanchez-Monge R, et al. 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
    17. 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
    18. 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
    19. Sanchez-Monge R, Diaz-Perales A, Blanco C, Salcedo G. Class I chitinases and the latex-fruit syndrome. Internet Symp Food Allergens 2000;2:137-144
    20. 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):127-133
    21. O'Riordain G, Radauer C, Hoffmann-Sommergruber K, Adhami F, et al. Cloning and molecular characterization of the Hevea brasiliensis allergen Hev b 11, a class I chitinase. Clin Exp Allergy 2002;32(3):455-62
    22. 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
    23. Mavale-Manuel S, Paty E, Scheinmann P, de Blic J. Latex allergy in children. [French] Arch Pediatr 2003;10(8):700-6
    24. Zaglaniczny K. Latex allergy: are you at risk? AANA J 2001;69(5):413-24
    25. Sanchez Palacios A. Latex allergy. Diagnosis and therapeutic aspects. [Spanish] Allergol Immunopathol (Madr) 2001;29(5):212-21
    26. Blanco C, Carrillo T, Castillo R, Quiralte J, Cuevas M. Avocado hypersensitivity. Allergy 1994;49:454-9
    27. 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
    28. 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
    29. Wagner S, Breiteneder H. The latex-fruit syndrome. Biochem Soc Trans 2001;30(6):935-40
    30. 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
    31. 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
    32. 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
    33. 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
    34. 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
    35. 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
    36. 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
    37. Kim KT, Hussain H Prevalence of food allergy in 137 latex-allergic patients. Allergy Asthma Proc 1999;20(2):95-7
    38. 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
    39. 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
    40. Brehler R, Theissen U, Mohr C, Luger T. "Latex-fruit syndrome": frequency of cross-reacting IgE antibodies. Allergy 1997;52(4):404-10
    41. Monreal P, Server MT, et al. Hipersensitivity to fruits in latex allergic patients. Allergol Immunopathol Madr 1996;24(1):33-5
    42. 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
    43. 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
    44. Gall H, Kalevam KJ, Forck G, Sterry W. Kiwi fruit allergy: a new birch pollen-associated food allergy. J Allergy Clin Immunol 1994;94:70-76
    45. Twarog FJ. Food-induced allergy in childhood. Allergy Asthma Proc 1998;19(4):219-222
    46. 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
    47. 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
    48. Telez-Diaz G, Ellis MH, Morales Russo F, Heiner DC. Prevalence of avocado allergy among atopic patients. Allergy Proc 1995;16(5):241-3
    49. 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
    50. Latasa M, Dieguez I, et al. Fruit sensitization in patients with allergy to latex. J Investig Allergol Clin Immunol 1995;5(2):97-102
    51. 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
    52. Castillo R, Delgado J, et al. Food hypersensitivity among adult patients: epidemiological and clinical aspects. Allergol Immunopathol Madr 1996;24(3):93-7
    53. Lavaud F, Cossart C, et al. Latex allergy in patients with allergy to fruit. Lancet 1992;339:492-493
    54. Ceuppens JL, Van Durme P, Dooms-Goossens A. Latex allergy in patient with allergy to fruit. Lancet 1992;339(8791):493
    55. 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
    56. de Groot AC, van der Meeren LM, Weyland JW. Contact allergy to avocado oil in a sunscreen Contact Dermatitis 1987;16(2):108-109
    57. Nater JP, De Groot AC. Unwanted effects of cosmetics and drugs used in dermatology. 2nd Ed. Amsterdam. Elsevier Science Publ 360-7, 425-5
    58. Wells PS, Holbrook AM, et al. Interactions of warfarin with drugs and food. Ann Intern Med 1994;121(9):676-83
    59. Blickstein D, Shaklai M, Inbal A Warfarin antagonism by avocado. Lancet 1991;337(8746):914-5
    60. 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
    61. 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
    62. 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
    63. Buoro IB, Nyamwange SB, Chai D, Munyua SM Putative avocado toxicity in two dogs. Onderstepoort J Vet Res 1994;61(1):107-9

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