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Code: f92
Latin name: Musa acuminata/sapientum/paradisiaca
Source material: Fruit
Family: Musaceae
Common names: Banana, Plantain

Commercial dessert (or common) banana cultivars most frequently eaten in temperate countries are of the species M. acuminata or the hybrid M. x paradisiaca, a cultigen of M. acuminata and M. balbisiana). However, M. × paradisiaca is also the generic name for the common plantain, a coarser and starchier variant not to be confused with M. acuminata, or the Cavendish variety. Common banana is most often eaten raw, whereas plantain is eaten cooked.


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

Allergen Exposure

Banana is the common name for a fruit, and also for the herbaceous plants of the genus Musa that produce this popular fruit. Banana plants are of the family Musaceae. They are cultivated primarily for their fruit, and to a lesser extent for the production of fibre and as ornamental plants. (1)

Banana originated in South-east Asia. Bananas are now grown in a variety of tropical regions throughout the world, and the ease of harvesting, shipping and storing makes them the cheapest and most readily available fruits. ‘Ripening rooms’ allow distributors to control the state of bananas for optimum convenience. Ripening rooms are special rooms made air-tight and filled with ethylene gas to induce ripening.

Bananas are often mistaken for trees, when in fact the main or upright stem is a pseudostem. It grows from a corm, which in some species can attain a height of 2 to 8 m, with leaves of up to 3.5 m in length. Each pseudostem can produce a bunch of yellow, green, or even red bananas before dying and being replaced by another pseudostem. (1)

The banana fruit grows in hanging clusters, with up to 20 fruit to a tier (called a hand), and 3 to 20 tiers to a bunch. The total of the hanging clusters is known as a bunch, or commercially as a ‘banana stem’, and can weigh from 30 to 50 kg. Banana has a protective outer layer (a peel or skin) with a fleshy edible inner portion. Western cultures generally eat the inside raw and throw away the skin, while some Asian cultures generally eat both the skin and inside, cooked. (1)

There are two main species. Plantains are often firmer than dessert bananas; they also have less sugar. Common banana is sweet and rather mealy and is most often eaten raw, whereas Plantain is hard and starchy and is eaten cooked. The colour, size and shape of the fruits, however, are similar.

Bananas eaten raw are an important natural convenience food in industrialised countries, not requiring (and in fact being spoiled by) refrigeration, and being very easy to peel and eat out of hand. Bananas are also found in fruit salads and many other desserts. Plantains are not a familiar food in the West, but in a number of other regions they form an important part of staple diets. Bananas are extremely nutritious, containing an especially high level of potassium, and several other important substances. Banana’s consistency makes it an ideal food to introduce into the diet of young infants.

Bananas have a very wide range of medicinal uses, including in the treatment of high blood pressure and constipation. Natural Banana essence is added to some processed foods and to some medicines as a flavourant. The peels have household uses such as cleaning and shining. Banana is a common ingredient of cosmetics and toiletries, but as in the case of edible products, the ‘banana’ may be artificial.

Allergen Description 

The following allergens have been characterised:

From Musa x paradisiaca

Mus xp 1, a profilin. (2, 3, 4, 5, 6, 7)

Mus xp 2, a 32-33 kDa protein, a class 1 chitinase, a hevein-like protein. (6, 8, 9, 10)

Mus xp 5, a beta-1,3-glucanase. (11, 12, 13, 14)

Mus xp TLP, a thaumatin-like protein. (15, 16, 17)

From Musa acuminata

Mus a 1, a profilin. (2, 3, 4, 5)

Mus a 2, previously known as Mus a 1, a 32-33 kDa protein, a class 1 chitinase, a hevein-like protein. (2, 18, 19, 20)

Mus a 3, a lipid transfer protein. (2, 21)

Mus a 4, a thaumatin-like protein. (2, 16, 22, 23, 24)

Mus a 5, a beta-1,3-glucanase. (2, 12, 13, 14, 17, 25, 26)

IgE binding to the recombinant banana profilin was demonstrated in 7 of 16 banana-allergic subjects. (5)  

Although no other allergens have been characterised to date, there have been a number of antigenic proteins identified. In a latex-allergic patient study, 16 allergenic components were identified in banana, with molecular weights ranging from 17 to 128 kDa. Two were considered to be major allergens: a 33 kDa protein was detected in 15 of 19 sera (88%), and a 37 kDa in 13 of 19 sera (76%). (6)

The 33 kDa allergen may be a chitinase similar to that reported in a study describing the isolation of 32 kDa and 34 kDa allergens, class I chitinases with a hevein-like domain, shown to be major allergens in banana fruit. The 2 purified allergens detected banana skin-specific IgE in more than 50% of 15 banana-allergic patients. (9, 27) Proteins of 40, 52, 58, 88 and 94 kDa have also been detected. (2) Other studies have isolated from banana extract a 40 kDa protein showing strong IgE binding; and allergens of 52, 58, 88 and 94 kDa were detected. (28) In a patient sensitised to avocado, but not to latex or pollen, a single allergen of 70 kDa was detected. (2)  

Among sera from 22 latex-allergic patients, 10 (45%) recognised 14 allergens in banana. The most frequently identified banana allergens were 23, 32, 36, 39 and 47 kDa proteins. Skin-specific IgE to banana was found in 14 of 18 latex-allergic patients studied, and Banana RAST in 12 of 14 patient sera tested. (29)

The pulp of ripe Bananas contains an abundant thaumatin-like protein (TLP). (16) Thaumatin allergens have allergenic potential, but in banana, TLP may be different and was not evaluated. Although the banana thaumatin-like protein adopts an overall fold similar to that of thaumatin and thaumatin-like PR-5 proteins, and TLPs have anti-fungal properties, the banana TLP appeared to be devoid of anti-fungal activity. Pulp of plantains contains a very similar TLP, which is even more abundant than its banana homologue. (22)

A study of 51 children with allergic reactions after banana ingestion who were positive to both specific IgE and skin-prick test (SPT) to banana, reported that specific IgE to both banana allergens Mus a 4 and Mus a 5, as well as to peach Pru p 3, was found in over 70% of the sera of this group, and that Mus a 4 and Pru p 3 provoked positive SPT responses in 6 of the 12 tested patients, whereas Mus a 5 did the same in only one of them. Profilin of date palm tree, Pho d 2, were positive in vitro in 41% and in vivo in 58% of tests. Therefore, Mus a 4 and lipid transfer proteins (LTP) behave as major banana allergens in the study population, and profilin seems also to be a relevant allergen. On the other hand, no banana reactivity has been found in adult LTP-allergic patients from Italy, and consequently this fruit has been proposed as a safe food for LTP-allergic subjects. (17)

One of the predominant proteins in the pulp of ripe bananas and plantains has been identified as a lectin. The clinical relevance of this banana lectin to food safety is at present unknown. (30)

Potential Cross-Reactivity

Extensive cross-reactivity among the different individual species of the genus (basically banana and plantain) could be expected. (31)

Allergy to latex is a increasing occupational and public health problem. Through the analysis of specific IgE against latex, the prevalence of latex sensitisation in the general population has been estimated to be approximately 4-7%. (32) Certain groups are at higher risk. Approximately 24-60% of patients with spina bifida may be sensitised to latex. Between 3 and 25% of healthcare workers may be sensitised. (33, 34) Other high-risk groups include greenhouse and rubber workers. Approximately 42-50% of patients with latex allergy have hypersensitivity to some foods; avocado, banana, chestnut and kiwi are those most frequently detected. (35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47 )In a study examining food items that led to anaphylactic reactions in latex-allergic individuals, several patterns of cross-reactivity have been demonstrated: Banana and avocado; banana, avocado and buckwheat; and banana, avocado and tomato. (48) Furthermore, cross-reactivity may occur between banana and avocado without concomitant sensitisation to latex. (49)

A number of panallergens may be involved in latex-fruit cross-reactivity. Banana, avocado, chestnut and kiwi are the most frequently implicated foods, but associations with several other fruits and vegetables have been reported. The allergen responsible for most cases of this syndrome is an isolated hevein (Hev b 6.02), the amino-terminal fragment of prohevein, but not the 31 kDa endochitinase. The homologous protein in banana is Mus xp Hevein. (8, 50) This panallergen has recently been shown to occur in custard apple, with affected individuals also experiencing anaphylaxis to banana. (51) Endo-beta-1,3-glucanase, the Banana glucanase, may account for some of the IgE-binding cross-reactivity frequently reported in patients with latex-fruit syndrome. (12) This allergen has also been shown to occur in olive (Ole e 9), ash and birch pollens, and in tomato, potato, bell pepper and latex. (13)

Approximately 45% of latex-allergic individuals are also allergic to banana, kiwi and avocado. (44, 52, 53) In a study of 47 latex-allergic patients, immunological reactivity to foods was found in 33. Positive banana skin-specific IgE was demonstrated most frequently with avocado (53%) and banana (38%). (44) In another study, 8 of 16 latex-allergic patients (50%) reported symptoms after eating bananas, and skin-specific IgE was found to banana in 5 of 14 patients (36%). Banana RAST results were positive in 12 of the 19 patients (63%). Seventeen of the 19 patients (89%) exhibited specific banana IgE antibodies. (6)

Other studies have had similar findings. Among 82 adult patients with latex allergy, Banana skin-specific IgE was found in 17. (54)

Not all latex-allergic individuals are also allergic to banana. In a study examining the sera of 47 latex-allergic individuals by RAST, 66% were shown to be positive to latex and 55% to banana. Of the 31 latex-positive sera, 25 were also banana-positive. Skin-specific IgE to banana was found in 11 of the 31 patients tested, and symptoms after eating bananas were reported by 16 (52%) of the 31 patients. Cross-reactivity between banana and latex was demonstrated in inhibition studies and other studies. (55) Similarly, in 2 children with latex hypersensitivity, banana skin-specific IgE and skin-specific IgE to a number of other fruits were positive, but the children presented no symptoms after ingestion of these fruits. (56)

The association between latex and banana allergy has been shown to be due to a class I chitinase panallergen. (9, 27, 57) In a study of patients allergic to latex, 9 of 15 sera with IgE to hevein showed IgE binding to 32 and 33 kDa banana proteins. The 33 kDa protein showed over 90% identity to endochitinases of several plants. (10) The role of chitinase has been demonstrated in other studies. (58) The banana, avocado, and chestnut chitinases share 65-70% sequence identity with the latex hevein chitinase. (59) Therefore, although banana contains a number of allergens, individuals allergic to the class I chitinase allergen in banana will probably be cross-reactive with other class I chitinase-containing foods, e.g. avocado, chestnut, cherimoya, passionfruit, kiwi, papaya, mango, tomato and wheat. (These allergens are not heat-activated; they appear to be activated by ‘stress’ to the plant.) (60) Chitinases have been shown to play a major role in the cross-reactivity between banana, chestnut and kiwi. (61)

The corollary holds, that in banana-allergic children (or children with allergies to other fruits), co-existing latex allergy should be considered, in particular in cases of urticaria or anaphylaxis for which the cause is unknown. (41, 62) Among 57 fruit-allergic patients, immunologic latex sensitisation occurred in 49 (85.9%). Six out of 57 (10.5%) suffered from clinically relevant latex allergy. In all patients, clinical symptoms to fruits preceded a history of latex allergy. The fruits most often associated were melon, peach, and banana. (63)

Banana contains a profilin panallergen. Banana profilin has been demonstrated to have a 71-84% sequence identity to other pollen and ingested profilins. Cross-reactivity between pollen and exotic foods containing profilin is possible. (5) Ten to 15% of birch pollen-allergic individuals have specific IgE to the 35 kDa minor birch pollen allergen, and there is cross-reactivity with proteins of comparable size from litchi, mango, banana, orange, apple, pear and carrot. (64) In a study of birch pollen allergy, hypersensitivity to Bet v 2 was strongly associated with clinical allergy to citrus fruits, melon and watermelon, banana, and tomato. The efficacy of a history of allergy to gourd fruits, citrus fruits, tomato, banana, or a combination thereof as a means of detecting profilin-hypersensitive patients was 85% (41/48). The study concluded that in clinical settings in which laboratory investigations are not easy to carry out, allergy to melon, watermelon, citrus fruits, tomato, and banana can be used as a marker of profilin hypersensitivity once a sensitisation to natural rubber latex and lipid transfer protein has been ruled out. (7, 65)

In some instances, cross-reactivity has been described for which a panallergen had not been determined. In individuals sensitised to Ficus allergens, sensitisation to kiwi fruit, papaya, and avocado, as well as to pineapple and banana, may occur. (66) Sensitisation to Ficus benjamina latex has been shown to be 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%). This cross-reactivity is mediated at least in part by the thiol proteases ficin and Papain. (67)

Similarly, sensitisation to the latex of F. benjamina, H. brasiliensis, breadfruit and banana was demonstrated in a patient allergic to banana, F. benjamina and breadfruit. RAST inhibition studies showed that specific IgE to breadfruit latex cross-reacted more strongly with latex of H. brasiliensis and banana than it did with latex of F. benjamina. (68) Two of 4 patients with an allergy to Ficus benjamina had a cross-allergy to latex and the associated cluster of tropical fruit (banana, kiwi, avocado) and chestnut, implying that the panallergen chitinase is responsible for these items cross-reacting. (69)

A positive allergenic correlation between Platanus (London plane tree) pollen and hazelnut, peanut, banana and celery has been described. RAST inhibition experiments indicated an important cross-reactivity between the pollen of Platanus acerifolia and hazelnut and banana fruit, and an intermediate cross-reactivity with celery and peanut as foods. (70) Whether this cross-reactivity occurs as a result of the panallergen profilin was not determined.

In a study of 53 patients (19 positive on a DBPCFC) with melon allergy, the most common foods associated with this allergy were avocado (n=7), banana (n=7), kiwi (n=6), watermelon (n=6), and peach (n=5). (71)

Similarly, in a study investigating the prevalence of avocado allergy, in 100 consecutive atopic patients with allergic rhinitis, 4 reported similar symptoms upon eating banana. (72)

In 11 Greek patients studied for allergy to grape, wine, or other grape products, other foods that induced anaphylaxis were apples (54.5%), cherries (18.6%), peaches (18.6%), and bananas (9.3%). Potential allergens were not investigated. (73)

Associations between weed pollen allergy and hypersensitivity to certain kinds of food have also been observed, such as the ragweed-melon-banana association. (74) The panallergen was not identified. Goosefoot profilin has been shown to be inhibited by banana by 68%. (75)

Clinical Experience

IgE-mediated reactions

Banana may commonly induce symptoms of food allergy in latex-sensitised individuals, but may also induce symptoms of food allergy in non-latex-sensitised individuals. (2, 76, 77, 78) Allergenicity of banana increases with ripeness. Case reports describe a wide heterogeneity of responses to banana. (4) For example, in a study of 4 patients who were banana-allergic, 1 reported itching of the mouth and throat, followed 30 minutes later by urticaria, angioedema, and hypotension; a second reported oral itching (OAS) only; and a third experienced urticaria, conjunctivitis and OAS. One patient was co-sensitised to avocado, but not to latex or pollen. One patient worked with bananas. (4)

In one of the earliest reports of adverse reactions to banana, 2 067 allergic patients studied in 1968-1969 included 36 patients who complained of various symptoms after eating banana. Among these symptoms were itching throat, ‘gassiness’ and indigestion, cramps, diarrhoea, vomiting, sore mouth or tongue, ‘canker sores’, swollen lips, wheezing, hoarseness, urticaria and other rashes, and angioedema. (76) Another report indicates that adverse reactions may include oral allergy syndrome, urticaria and, in severe instances, anaphylaxis. (5)

In 142 adults among 7 698 patients visiting an outpatient clinic and reporting sensitisation to foods, 120 experienced clinical symptoms after consumption of 1 or more foods. The most frequently recorded symptoms were urticaria/angioedema (70%), oral allergy syndrome (54%), asthma (37%) and anaphylaxis (27.5%). Banana sensitisation occurred in 12 patients. (79) In a cross-sectional, descriptive, questionnaire-based survey conducted in Toulouse schools in France to determine the prevalence of food allergies among schoolchildren, it was reported that, out of 2 716 respondents, 192 self-reported a food allergy, but that there was only a single reported case of allergy to banana. (80) A study was conducted at 17 clinics in 15 European cities to evaluate the differences between some Northern countries regarding what foods, according to the patients, elicit hypersensitivity symptoms. It was reported, based on a questionnaire concerning 86 different foods, that among 1 139 individuals, banana was the 38th-most-reported food allergen, resulting in adverse effects in 14%. (81) In a Japanese survey of 1 383 patients concerning self-reported severe food allergies, 319 patients reported food allergy, of whom 9 (2.8%) reported allergy to banana. (82) Of 3 025 children with asthma followed up at a clinic in Ankara, Turkey, only 2 were skin-prick test-positive for banana. (83) In Delhi, India, of 216 asthmatics with food sensitisation, skin-prick tests were positive to banana in 11. (84) In an Indian study of 24 children aged 3 to 15 years with documented deterioration in control of their perennial asthma, serum-specific IgE to banana was found in 20 (83%). (85)

Banana allergy may occur early in life, as reported in 2 infants. A 6-month-old girl developed vomiting, generalised urticaria with erythema, and wheezing an hour after ingesting fresh banana with yoghurt. Serum-specific IgE was 1.97 UA/ml. This was the third time she had ingested banana. The ( )second patient was a 6-month-old boy who developed urticarial rash on his whole body and erythema around the lips 1 hour after eating fresh banana (with yoghurt) for the first time. His mother had frequently eaten banana since the baby's birth, and she had been breastfeeding him. Serum-specific IgE was 1.25 UA/ml. The authors speculated that sensitisation may have occurred through the mother’s breast milk. (86) Similarly, 30 minutes after ingestion of a spoonful of mashed fresh banana pulp, a 6-month-old boy with mild eczema developed urticarial rash with erythema on the face and neck, extending over the whole body. He had been breastfed only, and this was the first time he had eaten banana. He was shown to have specific IgE against avocado and banana, but not to latex or pollen. (49) A 5-month-old boy suffered 3 episodes of generalised urticaria 20 minutes after the ingestion of a fruit purée containing apple, banana and orange. Skin testing was positive for banana and chestnut. Specific IgE to banana was 58 KU/l, to orange 9.7 KU/l, to chestnut 5.6 KU/l, and to latex 1.6 KU/l. However, orange, apple and latex products were well tolerated. He had never eaten chestnut. The authors of reports of banana-allergic infants suggest that the route of sensitisation may have been via placenta, breast-milk, inadvertent oral intake of food, or even via inhalation. (49, 87)

Anaphylaxis may occur to banana. (51, 55, 77, 88, 89 )A 15-year-old girl developed anaphylactic shock, asthma, angioedema, and urticaria after eating a banana. She had eaten banana 2 weeks earlier without adverse effects. (90) Anaphylaxis was reported in a 32-year-old woman. She experienced swelling of her lips, developed severe oro-pharyngeal symptoms and generalised urticarial rash, and had difficulty breathing. Skin-specific IgE to banana and kiwi was demonstrated. Serum banana RAST was 0.68 ku/L. She had no latex-associated symptoms. (91) A 33-year-old woman with multiple episodes of anaphylaxis after ingestion of apple, banana and lychee was described. Skin-prick tests for apple and banana were positive. She was allergic to fruit without concomitant allergy to other common airborne/contact allergens. (77) Significantly, individuals who have developed anaphylaxis to banana may be negative to commercial skin tests. (88) A 6-year-old boy presented with a history of cutaneous and respiratory reactions to banana and avocado and was latex-allergic; he was shown to have high serum-specific IgE to latex, equivocal IgE to avocado and chestnut, and no IgE to banana or kiwi fruit. However, skin sensitisation was demonstrated to banana, avocado and chestnut. (92)

Anaphylaxis has been described in a 3-year-old boy with associated latex allergy. He had undergone 5 successive surgical operations during the first months of life and had had eaten banana previously without any untoward effects. He developed generalised urticarial rash, difficulty in breathing, and oro-pharyngeal symptoms, including itching and swelling of the lips, after eating a banana. On interrogation, it was found that swelling of the lips had occurred after blowing up rubber balloons; and a week later, periorbital oedema occurred after he touched a balloon. Banana skin-specific IgE was positive, and serum-specific IgE was 6.10 kU/L. For latex, it was 5.2 kU/L. (93)

Among 107 cases reported in 2002 to the French Allergy Vigilance Network, 59.8% involved anaphylaxis, 18.7% systemic reactions, 15.9% laryngeal angioedema, and 5.6% serious acute asthma. Latex-fruit was the fourth-most-common cause (9 patients), following peanut (n=14), nuts (n=16), and shellfish (n=9). In the latex-fruit group, the following were involved: avocado (n=4), kiwi (n=2), fig (n=2), and banana (n=1). (94)

In latex-fruit cross-reactivity, the expression of adverse reactions to the implicated allergens may not occur concomitantly. For example, a 48-year-old female nurse with asthma and rhinitis developed contact urticaria to latex gloves, but only two years later developed glottic oedema after the ingestion of chestnuts, and only subsequently experienced adverse effects to banana and kiwi (generalised urticaria). Specific IgE to latex was 49 KU/l, to chestnut 3.5KU/l, kiwi 1.5 KU/l and banana 0.86 KU/l. Skin-prick tests were positive. (61)

Banana may be a ‘hidden’ allergen. An IgE-mediated reaction to a banana-flavoured drug additive was described in an 8-year-old girl, who developed oral itching with wheals over her face and trunk, and angioedema on both eyelids, within 1 hour of her first oral dose of penicillin containing banana essence as a flavouring additive. Tests for penicillin allergy were negative, but serum-specific IgE to banana was positive (1.25 kU/L). The presence of banana proteins in the banana essence was demonstrated. (95) Similarly, a 42-year-old woman, with a history of 8 episodes of angiooedema over 2 years from latex gloves or from eating banana, developed similar symptoms while working on the production line of a company manufacturing a natural banana hair conditioner. Skin-prick was positive to latex, banana, cucumber, avocado, kiwi, and banana hair conditioner. (96)

Adverse effects to banana may manifest only in the skin. Symptoms include contact urticaria, (97) urticaria-angioedema, (98, 99) and worsening of eczema. (55) In a study investigating the prevalence of natural rubber latex sensitisation and allergy in 74 children with atopic dermatitis, 12 had circulating IgE antibodies to latex. Twenty children without proven Latex sensitisation showed increased food-specific IgE; most frequently to potato, banana, and chestnut. (100)

Other reactions

Banana has been reported to precipitate migraine in susceptible individuals. (101, 102) This may result from the normal presence of vasoactive substances such as serotonin and tyramine.

A forty-seven-year-old female was described who had experienced 3 attacks of acute pancreatitis after eating banana. Elevated serum and urine amylase levels returned to normal in parallel with the clinical symptoms. Total serum IgE was 644 IU/mL, and banana-specific IgE was 2.18 UA/ml. Endoscopic examination of the upper digestive tract showed the ampulla of Vater swollen and oedematous. Biopsy specimens showed mast cells accumulating in mucosa and submucosa. (103)

Compiled by Dr Harris Steinman,


  1. Wikipedia contributors, ‘Banana’, Accessed September 2012.
  2. International Union of Immunological Societies Allergen Nomenclature: IUIS official list Accessed September 2012.
  3. Sankian M, Varasteh A, Pazouki N, Mahmoudi M. Sequence homology: A poor predictive value for profilins cross-reactivity. Clin Mol Allergy 2005;3(1):13.
  4. 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.
  5. Reindl J, Rihs HP, Scheurer S, Wangorsch A, Haustein D, Vieths S. IgE reactivity to profilin in pollen-sensitized subjects with adverse reactions to banana and pineapple. Int Arch Allergy Immunol 2002;128(2):105-14.
  6. Delbourg MF, Guilloux L, Moneret-Vautrin DA, Ville G. Hypersensitivity to banana in latex-allergic patients. Identification of two major banana allergens of 33 and 37 kD. Ann Allergy Asthma Immunol 1996;76(4):321-6.
  7. Asero R, Mistrello G, Roncarolo D, Amato S, Zanoni D, Barocci F, Caldironi G. Detection of clinical markers of sensitization to profilin in patients allergic to plant-derived foods. J Allergy Clin Immunol 2003;112(2):427-32.
  8. 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.
  9. 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.
  10. Mikkola JH, Alenius H, Kalkkinen N, Turjanmaa K, Palosuo T, Reunala T. Hevein-like protein domains as a possible cause for allergen cross-reactivity between latex and banana. J Allergy Clin Immunol 1998;102(6 Pt 1):1005-12.
  11. Fuentes-Silva D, Rodriguez-Romero A. Endo-beta-1,3-glucanases recognized by serum IgE antibodies of allergic patients. Rev Alerg Asma Inmunol Ped 2006;15(1):35-42.
  12. Receveur-Bréchot V, Czjzek M, Barre A, Roussel A, Peumans WJ, Van Damme EJ, Rougé P. Crystal structure at 1.45-A resolution of the major allergen endo-beta-1,3-glucanase of banana as a molecular basis for the latex-fruit syndrome. Proteins 2006;63(1):235-42.
  13. Palomares O, Villalba M, Quiralte J, Polo F, Rodriguez R. 1,3-beta-glucanases as candidates in latex-pollen-vegetable food cross-reactivity. Clin Exp Allergy 2005;35(3):345-51.
  14. Peumans WJ, Barre A, Derycke V, Rougé P, Zhang W, May GD, Delcour JA, Van Leuven F, Van Damme EJ. Purification, characterization and structural analysis of an abundant beta-1,3-glucanase from banana fruit. Eur J Biochem 2000;267(4):1188-95.
  15. Ghosh R, Chakrabarti C. Crystal structure analysis of NP24-I: a thaumatin-like protein. Planta 2008;22(5):883-90.
  16. Menu-Bouaouiche L, Vriet C, Peumans WJ, Barre A, Van Damme EJ, Rouge P. A molecular basis for the endo-beta 1,3-glucanase activity of the thaumatin-like proteins from edible fruits. Biochimie 2003;85(1-2):123-31.
  17. Palacin A, Quirce S, Sanchez-Monge R, Bobolea I, az-Perales A, Martin-Munoz F, Pascual C, Salcedo G. Sensitization profiles to purified plant food allergens among pediatric patients with allergy to banana. Pediatr Allergy Immunol 2011;22(2):186-95.
  18. O'Riordain G, Sowka S, May GD, Scheiner O, Breiteneder H. Molecular characterization of two banana chitinase isoforms. EMBL/GenBank/DDBJ databases 2000. Accessed September 2012.
  19. Radauer C, Adhami F, Furtler I, Wagner S, Allwardt D, Scala E, Ebner C, Hafner C, Hemmer W, Mari A, Breiteneder H. Latex-allergic patients sensitized to the major allergen hevein and hevein-like domains of class I chitinases show no increased frequency of latex-associated plant food allergy. Mol Immunol 2011;48(4):600-9.
  20. Clendennen SK, May GD. Differential gene expression in ripening banana fruit. Plant Physiol 1997;115(2):463-9.
  21. Sanchez-Monge R, Salcedo G, Palacin A, Diaz-Perales A, Quirce S. Banana lipid transfer protein. EMBL/GenBank/DDBJ databases 2009. Accessed September 2012.
  22. Barre A, Peumans WJ, Menu-Bouaouiche L, Van Damme EJ, May GD, Herrera AF, Van Leuven F, Rouge P. Purification and structural analysis of an abundant thaumatin-like protein from ripe banana fruit. Planta 2000;211(6):791-9.
  23. Leone P, Menu-Bouaouiche L, Peumans WJ, Payan F, Barre A, Roussel A, Van Damme EJ, Rouge P. Resolution of the structure of the allergenic and antifungal banana fruit thaumatin-like protein at 1.7-A. Biochimie 2006;88(1):45-52.
  24. Ho VS, Wong JH, Ng TB. A thaumatin-like antifungal protein from the emperor banana. Peptides 2007;28(4):760-6.
  25. Barre A, Culerrier R, Granier C, Selman L, Peumans WJ, Van Damme EJ, Bienvenu F, Bienvenu J, Rougé P. Mapping of IgE-binding epitopes on the major latex allergen Hev b 2 and the cross-reacting 1,3beta-glucanase fruit allergens as a molecular basis for the latex-fruit syndrome. Mol Immunol 2009;46(8-9):1595-604.
  26. Aleksic I, Popovic M, Dimitrijevic R, Andjelkovic U, Vassilopoulou E, Sinaniotis A, Atanaskovic-Markovic M, Lindner B, Petersen A, Papadopoulos NG, Gavrovic-Jankulovic M. Molecular and immunological characterization of Mus a 5 allergen from banana fruit. Mol Nutr Food Res 2012;56(3):446-53.
  27. 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.
  28. 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.
  29. Alenius H, Makinen-Kiljunen S, Ahlroth M, Turjanmaa K, Reunala T, Palosuo T. Crossreactivity between allergens in natural rubber latex and banana studied by immunoblot inhibition. Clin Exp Allergy 1996;26(3):341-8.
  30. Peumans WJ, Zhang W, Barre A, Houles Astoul C, Balint-Kurti PJ, Rovira P, Rouge P, May GD, Van Leuven F, Truffa-Bachi P, Van Damme EJ. Fruit-specific lectins from banana and plantain. Planta 2000;211(4):546-54.
  31. Yman L. Botanical relations and immunological cross-reactions in pollen allergy. 2nd ed. Pharmacia Diagnostics AB. Uppsala. Sweden. 1982: ISBN 91-970475-09.
  32. Merrett TG, Merrett J, Kekwick R. The prevalence of immunoglobulin E antibodies to the proteins of rubber (Hevea brasiliensis) latex and grass (Phleum pratense) pollen in sera of British blood donors. Clin Exp Allergy 1999;29(11):1572-8.
  33. Poley GE Jr, Slater JE. Latex allergy. J Allergy Clin Immunol 2000;105(6 Pt 1):1054-62.
  34. Sanchez Palacios A. Latex allergy. Diagnosis and therapeutic aspects. [Spanish] Allergol Immunopathol (Madr) 2001;29(5):212-21.
  35. 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.
  36. Brehler R, Theissen U, Mohr C, Luger T. "Latex-fruit syndrome": frequency of cross-reacting IgE antibodies. Allergy 1997;52(4):404-10.
  37. Kurup VP, Kelly T, Elms N, Kelly K, Fink J. Cross-reactivity of food allergens in latex allergy. Allergy Proc 1994;15(4):211-6.
  38. 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.
  39. Fernandez de Corres L, Moneo I, Munoz D, Bernaola G, Fernandez E, Audicana M, Urrutia I. Sensitization from chestnuts and bananas in patients with urticaria and anaphylaxis from contact with latex. Ann Allergy 1993;70(1):35-9.
  40. Rodriguez M, Vega F, Garcia MT, Panizo C, Laffond E, Montalvo A, Cuevas M. Hypersensitivity to latex, chestnut, and banana. Ann Allergy 1993;70(1):31-4.
  41. Blanco C. The latex-fruit syndrome: a review on clinical features. Internet Symp Food Allergens 2000;2:125-35.
  42. M'Raihi L, Charpin D, Pons A, Bongrand P, Vervloet D. Crossreactivity between latex and banana. J Allergy Clin Immunol 1991;87:129-130.
  43. Ross BD, McCullough J, Ownby DR. Partial cross-reactivity between latex and banana allergens. J Allergy Clin Immunol 1992;90(3 Pt 1):409-10.
  44. 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.
  45. Blanco Guerra C. Latex-fruit syndrome. [Spanish] Allergol Immunopathol (Madr). 2002;30(3):156-63.
  46. Kim KT, Hussain H. Prevalence of food allergy in 137 latex-allergic patients. Allergy Asthma Proc 1999;20(2):95-7.
  47. Wagner S, Breiteneder H. The latex-fruit syndrome. Biochem Soc Trans 2002;30(Pt 6):935-40.
  48. 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.
  49. 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.
  50. Asero R, Mistrello G, Roncarolo D, Amato S, Falagiani P. Detection of novel latex allergens associated with clinically relevant allergy to plant-derived foods J Allergy Clin Immunol 2005;115(6):1312-4.
  51. 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.
  52. 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.
  53. Baker L, Hourihane J O'B. Latex allergy: Two educational cases. Pediatr Allergy Immunol 2008;19(6):477-81.
  54. 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.
  55. Makinen-Kiljunen S. Banana allergy in patients with immediate-type hypersensitivity to natural rubber latex: characterization of cross-reacting antibodies and allergens. J Allergy Clin Immunol 1994;93(6):990-6.
  56. 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.
  57. Blanco C. Latex-fruit syndrome. Curr Allergy Asthma Rep 2003;3(1):47-53.
  58. 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.
  59. 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.
  60. 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.
  61. Santos A, Geraldes L, Carrapatoso I, Pereira C, Loureiro C, Chieira C. Diagnosing fruit allergy in a patient allergic to latex. (Poster) 2nd Int Symp Molecular Allergol, Rome, Italy 2007;April 22-24.
  62. Sorva R, Makinen-Kiljunen S, Suvilehto K, Juntunen-Backman K, Haahtela T. Latex allergy in children with no known risk factor for latex sensitization. Pediatr Allergy Immunol 1995;6(1):36-8.
  63. Garcia Ortiz JC, Moyano JC, Alvarez M, Bellido J. Latex allergy in fruit-allergic patients. Allergy 1998;53(5):532-6.
  64. Wellhausen A, Schoning B, Petersen A, Vieths S. IgE binding to a new cross-reactive structure: a 35 kDa protein in birch pollen, exotic fruit and other plant foods. Z Ernahrungswiss 1996;35(4):348-55.
  65. Westphal S, Kempf W, Foetisch K, Retzek M, Vieths S, Scheurer S. Tomato profilin Lyc e 1: IgE cross-reactivity and allergenic potency. Allergy 2004;59(5):526-32.
  66. 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.
  67. 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.
  68. De Greef JM, Lieutier-Colas F, Bessot JC, Verot A, Gallerand AM, Pauli G, de Blay F. Urticaria and rhinitis to shrubs of Ficus benjamina and breadfruit in a banana-allergic road worker: evidence for a cross-sensitization between Moracea, banana and latex. Int Arch Allergy Immunol 2001;125(2):182-4.
  69. 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.
  70. Miralles JC, Caravaca F, Guillen F, Lombardero M, Negro JM. Cross-reactivity between Platanus pollen and vegetables. Allergy 2002;57(2):146-9.
  71. Rodriguez J, Crespo JF, Burks W, Rivas-Plata C, Fernandez-Anaya S, Vives R, Daroca P. Randomized, double-blind, crossover challenge study in 53 subjects reporting adverse reactions to melon (Cucumis melo). J Allergy Clin Immunol 2000;106(5):968-72.
  72. Telez-Diaz G, Ellis MH, Morales-Russo F, Heiner DC. Prevalence of avocado allergy among atopic patients. Allergy Proc 1995;16(5):241-3.
  73. Kalogeromitros DC, Makris MP, Gregoriou SG, Mousatou VG, Lyris NG, Tarassi KE, Papasteriades CA. Grape anaphylaxis: a study of 11 adult onset cases. Allergy Asthma Proc 2005;26(1):53-8.
  74. Egger M, Mutschlechner S, Wopfner N, Gadermaier G, Briza P, Ferreira F. Pollen-food syndromes associated with weed pollinosis: an update from the molecular point of view. Allergy 2006;61(4):461-76.
  75. Barderas R, Villalba M, Rodriguez R. Recombinant expression, purification and cross-reactivity of chenopod profilin: rChe a 2 as a good marker for profilin sensitization. Biol Chem 2004;385(8):731-7.
  76. Anderson LBJ, Dreyfuss EM, Logan J, Johnstone DE, Glaser J. Melon and banana sensitivity coincident with ragweed pollinosis. J Allergy 1970;45:310-9.
  77. Saraswat A, Kumar B. Anaphylactic reaction to apple, banana and lychee: what is common between botanically disparate plant families? Int J Dermatol 2005;44(12):996-8.
  78. 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.
  79. 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.
  80. 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.
  81. 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.
  82. Imamura T, Kanagawa Y, Ebisawa M. A survey of patients with self-reported severe food allergies in Japan. Pediatr Allergy Immunol 2008;19(3):270-4.
  83. Dibek Misirlioğlu E, Reha Cengizlier M. Skin prick test results of child patients diagnosed with bronchial asthma. Allergol Immunopathol (Madr) 2007;35(1):21-4.
  84. Kumar R, Singh BP, Srivastava P, Sridhara S, Arora N, Gaur SN. Relevance of serum IgE estimation in allergic bronchial asthma with special reference to food allergy. Asian Pac J Allergy Immunol 2006;24(4):191-9.
  85. Agarkhedkar SR, Bapat HB, Bapat BN. Avoidance of food allergens in childhood asthma. Indian Pediatr 2005;42(4):362-6.
  86. Tokuyama K, Takei K, Arakawa H, Kato M, Shimizu T, Hoshino M, Mochizuki H, Morikawa A. Banana allergy in infants. Allergy 1997;52(3):350-1.
  87. Moreno-Ancillo A, Dominguez-Noche C, Gil-Adrados AC, Cosmes PM. Allergy to banana in a 5-month-old infant. Pediatr Allergy Immunol 2004;15(3):284-5.
  88. Hauswirth DW, Burks AW. Banana anaphylaxis with a negative commercial skin test. J Allergy Clin Immunol 2005;115(3):632-3.
  89. Gelincik A, Büyüköztürk S, Gül H, Işιk E, Işsever H, Ozşeker F, Colakoğlu B, Dal M, Ayvaz O, Güngör G, Akkor A. Confirmed prevalence of food allergy and non-allergic food hypersensitivity in a Mediterranean population. Clin Exp Allergy 2008;38(8):1333-41.
  90. Linaweaver WE, Saks GL, Heiner DC. Anaphylactic shock following banana ingestion. Am J Dis Child 1976;130:207-9.
  91. Savonius B, Kanerva L. Anaphylaxis caused by banana. Allergy 1993;48:215-6.
  92. Freeman GL. Cooccurrence of latex and fruit allergies. [Review] Allergy Asthma Proc 1997;18(2):85-8.
  93. Cinquetti M, Peroni D, Vinco A, Zoppi G. Latex allergy in a child with banana anaphylaxis. Acta Paediatrica 1995;84(6):709-10.
  94. 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.
  95. Matheu V, Zapatero L, Alcazar M, Martinez-Molero MI, Baeza ML. IgE-mediated reaction to a banana-flavored drug additive. J Allergy Clin Immunol 2000;106(6):1202-3.
  96. Smith HR, Wakelin SH, White IR. Banana hair conditioner and natural rubber latex allergy. Contact Dermatitis 1998;39(4):202.
  97. Meynadier J, Meynadier JM, Guilhou JJ. Contact urticaria in atopic patients. Apropos of 2 cases. [French] Ann Dermatol Venereol 1982;109(10):871-4.
  98. Estrada JL, Gozalo F, Cecchini C, Casquete E. Contact urticaria from hops (Humulus lupulus) in a patient with previous urticaria-angioedema from peanut, chestnut and banana. Contact Dermatitis 2002;46(2):127.
  99. Yilmaz A, Artan R, Uguz A, Arslan G, Akcam M. Severe angioedema caused by banana allergy under tacrolimus immunosuppression. Transplant Proc 2005;37(10):4251-3.
  100. 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.
  101. Guariso G, Bertoli S, Cernetti R, Battistella PA, Setari M, Zacchello F. Migraine and food intolerance: a controlled study in pediatric patients. [Italian] Pediatr Med Chir 1993;15(1):57-61.
  102. Leira R, Rodriguez R. Diet and migraine [Spanish] Revista de Neurologia 1996;24(129):534-8.
  103. Inamura H, Kashiwase Y, Morioka J, Kurosawa M. Acute pancreatitis possibly caused by allergy to bananas. J Investig Allergol Clin Immunol 2005;15(3):222-4.

As in all diagnostic testing, the diagnosis is made by the physican based on both test results and the patient history.