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Whole Allergen

t1 Box-elder Pollen

t1 Box-elder Pollen Scientific Information

Type:

Whole Allergen

Display Name:

Box-elder Pollen

Route of Exposure:

Inhalation

Family:

Aceraceae

Species:

Acer negundo

Latin Name:

Acer negundo

Other Names:

Maple ash, Ash maple, Ashleaf maple, Manitoba maple, Box elder maple, Western box elder, Black ash, California boxelder, Cutleaf maple, Cut-leaved maple, Negundo maple, Red river maple, Stinking ash, Sugar ash, Three-leaved maple

Summary

Box-elder (Acer negundo) is a rapid-growing, wind-pollinated tree, widely used for shading and ornamental purposes. The tree can attain a height of up to 20 m. The flowering season begins during early spring, with production of the seeds in enormous quantities every year. Box-elder tree is widely distributed across the globe, with its prevalence seen in parts of the US, Europe, Canada, Asia, China, Mexico, and Guatemala. Exposure to its pollen can trigger allergic respiratory symptoms, such as asthma, allergic rhinitis, and rhino-conjunctivitis. Studies have identified an association between increased concentration of tree pollens (box-elder and maple tree pollens) and high hospitalization rates due to severe asthma. Furthermore, contact dermatitis as a result of exposure to box-elder pollen oil has also been found in two patients. To date, no allergens have been identified; however, few potential allergenic protein bands have been reported. Cross-reactivity has been found to be high with maples, walnut and limited with other tree pollens, such as American sycamore, cottonwood, birch, English oak, and weeping willow.

Allergen

Nature

Box-elder (Acer negundo), also known as ash maple, belongs to the family of Aceraceae. It is a wind-pollinated, fast-growing tree that grows up to a height of 20 m, with an average lifespan of 60 years (1). Due to the quick reproduction and plantation of these trees, they are most commonly found alongside roads, parks in urban and rural areas (2). This tree is widely used for shading and as an ornamental tree (1, 3). The bark is light greyish-brown with shallow grooves inside that becomes deeply furrowed as the tree ages. The leaves of box-elder trees are pinnately compound, usually with 3-5 leaflets (length: 5-10 cm and width: 3-6 cm). The flowers are yellowish-green in color that are about 5 mm in length, with the male flowers being collective together as fascicles and the female flowers in the form of long drooping racemes. Most trees are dioecious; however, bisexual flowers may grow on a few trees. Flowering usually begins in early spring, where large quantities of seeds are produced every year. The ripening of seeds occur in autumn and falls continuously till spring (1). Furthermore, for fertilization to occur successfully, anemophilous plants release huge quantities of pollens in the air and produce aerodynamic pollen grains in order to make the dispersal easy (3).

The wood of box-elder tree is used for making furniture and paper pulps. Also, the syrup prepared by collecting saps from box-elder trees is popularly consumed, particularly in Canada (4).

Habitat

The Acer species are widely distributed across the globe. They grow at varying altitudes, ranging from high Himalayan peaks to Southeast Asian tropical rainforests to rock cliffs in the Mediterranean seacoasts and wetlands of North America (4). Box-elder tree thrives in sunlight, especially during the early stage of growth, but later it can tolerate partial shade. Box-elder is typically a river-bottom tree that grows on rich, moist soils in lowland areas that become waterlogged during the seasonal time (1). 

Taxonomy

Taxonomic tree of Box-elder (5)
Domain Eukaryota
Kingdom Plantae
Phylum Spermatophyta
Subphylum Angiospermae
Class Dicotyledonae 
Order Sapindales
Family Aceraceae
Genus Acer
Species Acer negundo
Taxonomic tree of Box-elder (5)

Tissue

All tree pollens belonging to the genus Acer exhibit wide variation in the pollen grain size, ranging from 21.6 to 55.2 µm (6).

With regard to Box-elder (Acer negundo), the diameter of the pollen grain ranges from 23 to 31 µm, with the shape of the pollen being slightly prolate-to-spherical. The surface of box-elder pollen may either be finely wrinkled or with a tectum perforate (holes). Through electron microscopy, the outer covering is found to be thicker and more electron-dense than the inner layer of the pollen grain (6). 

Epidemiology

Worldwide distribution

Box-elder tree produces allergenic airborne pollens. Aerobiological surveys have observed a positive correlation between elevated air pollen counts and increased risk of hospitalization in patients diagnosed with asthma and other respiratory diseases (7). An atmospheric survey was conducted in three United States (US) regions (Philadelphia, Pennsylvania, and New Jersey) to analyze the contributors of pollen in the air. According to the survey, 75% and 74.2% of tree pollens were detected in Philadelphia and New Jersey (Cherry Hills), respectively, with the leading contributors from the pollen taxa being Acer, Betula, Pinus, Rumex, Quercus, Poacaea, Cupressaceae, and Ambrosia (8).

In a study conducted in the US, the prevalence of sensitization to pollen allergens in young-asthmatic children (6 months-10 years) was assessed. Of all 687 asthmatic children, sensitization to box-elder pollen was found to be 27% (all ages), based on the positive skin prick test (SPT) results. Moreover, in these children, box-elder was found to be the most common sensitizing tree pollen (9).

In a study conducted in New York between the years 1993 and 2000, sera of 371 patients were tested for assessing the hypersensitivity against specific tree pollens, such as box-elder, birch, oak, beech, ash, poplar, elm, and hickory. The results reported a high prevalence of hypersensitivity towards box-elder tree pollen (32.8%) (10).

Risk factors

An interaction between box-elder pollen and atmospheric pollutants, such as SO2 and NO2, was observed in a study that established the effects of these pollutants on allergenicity, protein content, and germination rate of box-elder pollen. According to the study, 18 atopic patients in urban areas were sensitized to box-elder, based on an assessment done by SPT. The results pointed out that box-elder pollen antigens were influenced by the levels of atmospheric SO2 and NO2. Furthermore, it has been shown that in-vitro exposure to varying levels of these air pollutants might not only elevate pollinosis-related symptoms but also intensify allergenic reactions in box-elder pollen-sensitized individuals (3).

Environmental Characteristics

Worldwide distribution

The species from the Aceraceae family are commonly found in the temperate areas of the Northern Hemisphere and can also be found in the eastern part of Asia and China (6). Among all the American maple species, box-elder is found to be the most extensively distributed species, that extends from the eastern coastline of the US to Californian state and from the South of Canada to the mountains of Mexico as well as in Guatemala. In the US, this species is found in small regions of Western and Central America; however, it is not common in the northern part of North America. Furthermore, even though this tree is not native to Europe; however, it has now become naturalized there too (1). 

Route of Exposure

Main

The route of exposure for box-elder pollen is through inhalation (airway) (11).  

Secondary

Direct skin contact is another route of exposure. This was evidenced in two case studies where, after coming in contact with the pollen oil of box-elder, the patients developed contact dermatitis (12).

Clinical Relevance

Respiratory allergic diseases associated with tree pollens are on the rise, both in terms of severity and prevalence (7). At present, an estimated prevalence of pollen-related respiratory allergy is found to be ~40% (13). Furthermore, it has been reported that the plantation of box-elder trees for ornamental purposes in urban areas poses a high allergic impact on the residents of those areas (7).

Exposure to box-elder pollen can lead to asthma, allergic rhinitis (AR), and rhino-conjunctivitis, and occasionally contact dermatitis (14, 15). 

Asthma and Rhino-conjunctivitis

Airborne pollens are known to trigger allergic reactions, such as asthma and rhino-conjunctivitis (16). Furthermore, sensitization or allergic reactions to the tree pollens may often cause acute exacerbations of asthma, leading to hospitalization (14).

Two studies discussed about the correlation between increased level of tree pollens (including box-elder pollens) and severe asthmatic attack, leading to hospitalization. The first study was a Canadian study that examined the role of different tree pollen allergies and their association with increased hospitalization due to aggravation from severe asthma. The results showed an increased hospitalization (2.1%) for asthma due to box-elder and maple tree pollens (14). Similarly, the second study that was conducted in Portugal reported that, during peak tree pollination season, 31% of hospital admissions were due to asthma (444 out of 1433 every day admissions). Importantly, the correlation was found to be significant between Acer species pollen concentration and increased hospital admissions due to asthma (correlation coefficient=0.92, p<0.01) (7).

In a study conducted on 687 asthmatic-young children (6 months-10 years), the rate of sensitization to tree pollens was assessed. Interestingly, among all the tree pollen allergen extracts analyzed by SPT, box-elder was found to be the most common sensitizing allergen found in young-asthmatic children (12%) (9).  

In another study conducted in Turkey among 89 patients with rhino-conjunctivitis with/without asthma, 35% of patients were found to be sensitized to box-elder pollen, based on the positive SPT results (16).

Allergic rhinitis

In many parts of the world, allergic rhinitis (AR) has proven to be one of the most commonly found chronic diseases, causing a huge impact on patient’s health and quality of life. Furthermore, airborne tree pollens are considered as one of the major causes of developing AR (15). However, limited data on AR caused by box-elder pollen is available.

In a study conducted in Bolivia among 350 patients (aged between 11 to 60 years) suffering from AR, 15% of patients showed sensitization to box-elder pollen allergen, according to the positive SPT results (15).

Contact dermatitis

An association between box-elder pollen and contact dermatitis, although rare, does exist. This correlation was evidenced in two case studies who developed contact dermatitis (erythematous skin lesions on the face, hands, forearms, and the other exposed areas of the body) while coming in contact with the pollens of box-elder tree (during the fall season and in the months of April and May). The results were confirmed with a positive skin-patch test towards box-elder pollen oil in both the patients (12). 

Prevention and Therapy

Prevention strategies

Avoidance

Box-elder pollen allergy can be prevented or reduced by using some precautionary measures. One of the main protective measures against these pollen allergens is by minimizing the number of pollens in the respiratory system. Furthermore, during high pollination period, the pollen-allergic patients are suggested to either stay indoors or wear a mask while moving outdoors to avoid exposure to pollen allergens. Moreover, in extreme cases, where the patient’s health condition deteriorates, it is further advised to move to an area where there is less pollination (17).

Molecular Aspects

Allergenic molecules

No allergens have been identified for box-elder tree pollen to date (18). However, some potential allergenic protein bands, with molecular weights of 71, 52, 35, 32, 19, 16, and 14 kDa have been identified in box-elder pollen extract (7).

Cross-reactivity

Box-elder pollen has shown to display high cross-reactivity with closely-related species maple, which belongs to the same family Aceraceae as box-elder (19). According to literature, high inhibition of IgE binding to red maple was exhibited by box-elder (20). Furthermore, in a study conducted in the US, extensive cross-reactivity has been reported between walnut and box-elder (11).

Limited cross-reactivity has been observed between box-elder and other tree pollens. According to a study conducted in Portugal, box-elder pollen demonstrated high-binding affinity with weeping willow (Salix babylonica) and American sycamore (Platanus occidentalis) pollen extracts, however, limited affinity was observed towards cottonwood (Populus hybrida), birch (Betula pendula), and English oak (Quercus robur). This binding affinity may suggest cross-reactivity (although limited) between these tree pollens (7). 

Compiled By

Author: Turacoz Healthcare Solutions

Reviewer: Dr. Fabio Iachetti

 

Last reviewed: January 2021

References
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  2. Rolbiecki S, Stachowski P, Jagosz B, Figas A, Ptach W, Rolbiecki R, et al. Water needs of bird cherry trees at the period over three years after reclamation in different regions of Poland. Rocznik ochrona środowiska= Annual set the environment protection Koszalin: Middle Pomeranian Scientific Society of The Environment Protection, 2019, t 21. 2019.
  3. Sousa R, Duque L, Duarte AJ, Gomes CR, Ribeiro H, Cruz A, et al. In vitro exposure of Acer negundo pollen to atmospheric levels of SO2 and NO2: effects on allergenicity and germination. Environmental science & technology. 2012;46(4):2406-12.
  4. Gibbs D, Yousheng C. The red list of maples: Botanic Gardens Conservation International; 2009.
  5. CABI. Box elder 2019 [12-01-2021]. Available from: https://www.cabi.org/isc/datasheet/2862.
  6. Biesboer DD. Pollen morphology of the Aceraceae. Grana. 1975;15(1-3):19-27.
  7. Ribeiro H, Oliveira M, Ribeiro N, Cruz A, Ferreira A, Machado H, et al. Pollen allergenic potential nature of some trees species: A multidisciplinary approach using aerobiological, immunochemical and hospital admissions data. Environmental research. 2009;109(3):328-33.
  8. Dvorin DJ, Lee JJ, Belecanech GA, Goldstein MF, Dunsky EH. A comparative, volumetric survey of airborne pollen in Philadelphia, Pennsylvania (1991–1997) and Cherry Hill, New Jersey (1995–1997). Annals of Allergy, Asthma & Immunology. 2001;87(5):394-404.
  9. Ogershok PR, Warner DJ, Hogan MB, Wilson NW, editors. Prevalence of pollen sensitization in younger children who have asthma. Allergy & Asthma Proceedings; 2007.
  10. Lin RY, Clauss AE, Bennett ES, editors. Hypersensitivity to common tree pollens in New York City patients. Allergy and asthma proceedings; 2002: OceanSide Publications.
  11. Chapman JA. Aeroallergens of southeastern Missouri, USA. Grana. 1986;25(3):235-46.
  12. Lovell RG, Mathews KP, Sheldon JM. Dermatitis venenata from tree pollen oils: a clinical report. Journal of Allergy. 1955;26(5):408-14.
  13. D'Amato G, Cecchi L, Bonini S, Nunes C, Annesi-Maesano I, Behrendt H, et al. Allergenic pollen and pollen allergy in Europe. Allergy. 2007;62(9):976-90.
  14. Dales RE, Cakmak S, Judek S, Coates F. Tree pollen and hospitalization for asthma in urban Canada. International archives of allergy and immunology. 2008;146(3):241-7.
  15. Narváez-Gómez EI. Prevalence of sensitization to airborne allergens in patients with allergic rhinitis in southern Bolivia. VacciMonitor. 2016;25(2):49-54.
  16. Ince A, Kart L, Demir R, Ozyurt MS. Allergenic pollen in the atmosphere of Kayseri, Turkey. Asian Pac J Allergy Immunol. 2004;22(2-3):123-32.
  17. Xie Z-J, Guan K, Yin J. Advances in the clinical and mechanism research of pollen induced seasonal allergic Asthma. American journal of clinical and experimental immunology. 2019;8(1):1.
  18. WHO/IUIS. Acer Negundo 2020 [12-01-2021]. Available from: http://www.allergen.org/search.php?allergenname=&allergensource=acer+negundo&TaxSource=&TaxOrder=&foodallerg=all&bioname=.
  19. Ansotegui IJ, Melioli G, Canonica GW, Caraballo L, Villa E, Ebisawa M, et al. IgE allergy diagnostics and other relevant tests in allergy, a World Allergy Organization position paper. World Allergy Organization Journal. 2020;13(2):100080.
  20. White JF, Bernstein DI. Key pollen allergens in North America. Ann Allergy Asthma Immunol. 2003;91(5):425-35; quiz 35-6, 92.