Relationship between the sensitization to shrimp and mites. Exploration of cross-reactivity due tropomyosin
PDF (Spanish)
PubMed

Supplementary Files

XML (Spanish)

Keywords

Asthma
Rhinitis
Atopy
Food allergy
Shrimp
Mites
Tropomyosin
Cross-reactivity.

How to Cite

Relationship between the sensitization to shrimp and mites. Exploration of cross-reactivity due tropomyosin. (2019). Revista Alergia México , 66(2), 205-216. https://doi.org/10.29262/ram.v66i2.402

Plaudit

Abstract

Background: Little is known about the sensitization to shrimp in patients with respiratory allergies who are sensitized to mites and about the clinical relevance of that sensitization in the tropical region.

Objectives: To determine the prevalence of sensitization to shrimp in patients with rhinitis or asthma who are sensitized to mites, to explore the route of sensitization, its relevance, and the role of sensitization to tropomyosin.

Methods: A cross-sectional study in patients with asthma and rhinitis who are sensitized to mites. Through a survey, it was asked about the consumption of shrimp and the control of asthma or rhinitis. Oral provocation tests were carried out with shrimp on individuals who are sensitized to mites and shrimp without consumption, or consumption greater than six months before, without reaction history. In a subgroup, the sIgE was measured for shrimp, Der p and Lit v 1. The patients who are sensitized to mites and shrimp (cases) were compared to the patients who are sensitized only to mites (controls).

Results: Out of 229 patients, 48 (21%) were sensitized to shrimp. There wasn’t a statistically significant difference in the intake of shrimp between cases (54.2%) and controls (49.7%); eight cases showed symptoms on contact with shrimp. No statistically significant differences were found in the sIgE for Der p, Lit v1 and shrimp between cases and controls. A medium change was observed in the size of the effect: 0.45, 0.44 and 0.41 respectively.

Conclusions: Sensitization to shrimp in patients with asthma or allergic rhinitis caused by mites is high; in 25% it seems to be clinically relevant, mainly in those with asthma. Intake is not the main route of exposure to tropomyosin; cross-reactivity can explain the frequency of sensitization. 

PDF (Spanish)
PubMed

References

Mallol J, Crane J, von Mutius E, Odhiambo J, Keil U, Stewart A. The International Study of Asthma and Allergies in Childhood (ISAAC) phase three: a global synthesis. Allergol Immunopathol (Madr). 2013;41(2):73-85. DOI: 10.1016/j.aller.2012.03.001

Dennis RJ, Caraballo L, García E, Rojas MX, Rondon MA, Pérez A, et al. Prevalence of asthma and other allergic conditions in Colombia 2009-2010: a cross-sectional study. BMC Pulm Med. 2012;12(1):1. DOI: 10.1186/1471-2466-12-17

Ellwood P, Asher MI, Björkstén B, Burr M, Pearce N, Robertson CF. Diet and asthma, allergic rhinoconjunctivitis and atopic eczema symptom prevalence: an ecological analysis of the International Study of Asthma and Allergies in Childhood (ISAAC) data. ISAAC Phase One Study Group. Eur Respir J. 2001;17(3):436-443. DOI: 10.1016/0091-7435(83)90198-6

Cepeda AM, Thawer S, Boyle RJ, Villalba S, Jaller R, Tapias E, et al. Diet and respiratory health in children from 11 Latin American countries: evidence from ISAAC Phase III. Lung. 2017;195(6):683-692. DOI: 10.1007/s00408-017-0044-z

Mohammad Y, Shaaban R, Hassan M, et al. Respiratory effects in children from passive smoking of cigarettes and narghile: ISAAC phase three in Syria. Int J Tuberc Lung Dis. 2014;18(11):1279-1284. DOI: 10.5588/ijtld.13.0912.

Werfel T, Asero R, Ballmer-Weber BK, Beyer K, Enrique E, Knulst AC et al. Position paper of the EAACI: food allergy due to immunological cross-reactions with common inhalant allergens. Allergy. 2015;70(9):1079-1090. DOI: 10.1111/all.12666

Gámez C, Sánchez-García S, Ibáñez MD, López R, Aguado E, López E, et al. Tropomyosin IgE-positive results are a good predictor of shrimp allergy. Allergy. 2011;66(10):1375-1383. DOI: 10.1111/j.1398-9995.2011.02663.x

Munera MG, Gómez-Hernández L, Puerta Llerena L. El camarón como una fuente de alérgenos. Biomedica. 2012;33(2):161-178. DOI: 10.7705/biomedica.v33i2.795

Yang AC, Arruda LK, Santos ABR, Barbosa MC, Chapman MD, Galvão CE, et al. Measurement of IgE antibodies to shrimp tropomyosin is superior to skin prick testing with commercial extract and measurement of IgE to shrimp for predicting clinically relevant allergic reactions after shrimp ingestion. J Allergy Clin Immunol. 2010;125(4):872-878. DOI: 10.1016/j.jaci.2009.11.043

López-Rocha E, Rodríguez-Mireles K, Gaspar-López A, Del Rivero-Hernández LG, Segura-Méndez N. Frecuencia de sensibilización a ácaros, cucaracha y camarón en adultos con alergia respiratoria. Rev Alerg Mex. 2014;64:59-64. Disponible en: http://revistaalergia.mx/ojs/index.php/ram/article/view/27/40

Santos AB, Chapman MD, Aalberse RC, Vailes LD, Ferriani VP, Oliver C, et al. Cockroach allergens and asthma in Brazil: Identification of tropomyosin as a major allergen with potential cross-reactivity with mite and shrimp allergens. J Allergy Clin Immunol. 1999;104(2 Pt 1):329-337. DOI: 10.1016/S0091-6749(99)70375-1

Wong L, Huang CH, Lee BW. Shellfish and house dust mite allergies: is the link tropomyosin? Allergy Asthma Immunol Res. 2016;8(2):101. DOI: 10.4168/aair.2016.8.2.101

Sánchez-Caraballo J, Diez-Zuluaga S, Ricardo RCV. Sensibilización a aeroalergenos en pacientes alérgicos de Medellín, Colombia. Rev Alerg Mex. 2012;59(3):139-147.

Bonilla SP, De la Pava ML. Desarrollo de estrategias para el incremento del consumo de pescados y mariscos provenientes de la acuicultura de Colombia, como alternativa viable de comercialización en el mercado doméstico. Colombia: Autoridad Nacional de Acuicultura y Pesca; 2013. Disponible en: http://aunap.gov.co/wp-content/uploads/2016/05/Estrategia-para-incremento-del-consumo.pdf

Mopan J, Sánchez J, Chinchilla C, Cardona R. Prevalencia de sensibilización a leche y huevo en pacientes con sospecha de enfermedades mediadas por IgE. Rev Alerg Mex. 2015;62(1):41-47.

Bousquet J, Khaltaev N, Cruz AA, Denburg J, Fokkens WJ, Togias A, et al. ARIA (Allergic Rhinitis and its Impact on Asthma) 2008 update (in collaboration with the World Health Organization, GA 2 LEN and AllerGen). Allergy. 2008;63(Suppl 86):8-160. DOI: 10.1111/j.1398-9995.2007.01620.x

Nathan RA, Sorkness CA, Kosinski M, Schatz M, Li JT, Marcus P, et al. Development of the asthma control test: a survey for assessing asthma control. J Allergy Clin Immunol. 2004;113(1):59-65. DOI: 10.1016/j.jaci.2003.09.008

Bousquet J, Heinzerling L, Bachert C, Papadopoulos NG, Bousquet PJ, Burney PG, et al. Practical guide to skin prick tests in allergy to aeroallergens. Allergy. 2012;67(1):18-24. DOI: 10.1111/j.1398-9995.2011.02728.x

Heinzerling L, Mari A, Bergmann KC, Bresciani M, Burbach G, Darsow U, et al. The skin prick test-European standards. Clin Transl Allergy. 2013;3(1):3. DOI: 10.1186/2045-7022-3-3

Burney PGJ, Potts J, Kummeling I, Mills EN, Clausen M, Dubakiene R, et al. The prevalence and distribution of food sensitization in European adults. Allergy. 2014;69(3):365-371. DOI: 10.1111/all.12341

Pedrosa M, Boyano-Martínez T, García-Ara C, Quirce S. Shellfish allergy: a comprehensive review. Clin Rev Allergy Immunol. 2015;49(2):203-216. DOI: 10.1007/s12016-014-8429-8

Burney P, Summers C, Chinn S, Hooper R, Van-Ree R, Lidholm J. Prevalence and distribution of sensitization to foods in the European Community Respiratory Health Survey: a EuroPrevall analysis. Allergy. 2010;65(9):1182-1188. DOI: 10.1111/j.1398-9995.2010.02346.x

Mahesh PA, Wong GWK, Ogorodova L, Potts J, Leung TF, Fedorova O, et al. Prevalence of food sensitization and probable food allergy among adults in India: the EuroPrevall INCO study. Allergy. 2016;71(7):1010-1019. DOI: 10.1111/all.12868

Pascal M, Grishina G, Yang AC, Sánchez-García S, Lin J, Towle D, et al. Molecular diagnosis of shrimp allergy: Efficiency of several allergens to predict clinical reactivity. J Allergy Clin Immunol Pract. 2015;3(4):521-529. DOI: 10.1016/j.jaip.2015.02.001

Fernandes J, Reshef A, Patton L, Ayuso R, Reese G, Lehrer SB. Immunoglobulin E antibody reactivity to the major shrimp allergen, tropomyosin, in unexposed Orthodox Jews. Clin Exp Allergy. 2003;33(7):956-961. DOI: 10.1046/j.1365-2222.2003.01722.x

van Ree R, Antonicelli L, Akkerdaas JH, Garritani MS, Aalberse RC, Bonifazi F. Possible induction of food allergy during mite immunotherapy. Allergy. 1996;51(2):108-113. DOI: 10.1111/j.1398-9995.1996.tb04566.x

Guilleminault L, Viala-Gastan C. Blomia tropicalis: un acarien sous les tropiques. Rev Mal Respir. 2017;34(8):791-801. DOI: 10.1016/j.rmr.2016.10.877

Gámez C, Zafra-Paz M, Boquete M, Sanz V, Mazzeo C, Ibáñez MD, et al. New shrimp IgE-binding proteins involved in mite-seafood cross-reactivity. Mol Nutr Food Res. 2014;58(9):1915-1925. DOI: 10.1002/mnfr.201400122

Ayuso R, Lehrer SB, Reese G. Identification of continuous, allergenic regions of the major shrimp allergen pen a 1 (tropomyosin). Int Arch Allergy Immunol. 2002;127(1):27-37. DOI: 10.1159/000048166

Boquete M, Iraola V, Morales M, Pinto H, Francisco C, Carballás C, et al. Seafood hypersensitivity in mite sensitized individuals: is tropomyosin the only responsible allergen? Ann Allergy Asthma Immunol. 2011;106(3):223-229. DOI: 10.1016/j.anai.2010.11.014

Asero R, Mistrello G, Amato S, Ariano R, Colombo G, Conte ME, et al. Shrimp allergy in Italian adults: a multicenter study showing a high prevalence of sensitivity to novel high molecular weight allergens. Int Arch Allergy Immunol. 2011;157(1):3-10. DOI: 10.1159/000324470

Thomas WR, Smith WA, Hales BJ. The allergenic specificities of the house dust mite. Chang Gung Med J. 2004;27(8):563-569. Disponible en: http://cgmj.cgu.edu.tw/2708/270801.pdf

Londoño J, Sánchez J, Sánchez A, Calvo V, Diez L, Cardona R. Relation of sensibilization among 10 mites in a tropical city. Sensitization patterns according to allergic diseases. J Allergy Clin Immunol. 2017;139(2):AB119. DOI: 10.1016/j.jaci.2016.12.384

Yang Z, Zhao J, Wei N, Feng M, Xian M, Shi X, et al. Cockroach is a major cross-reactive allergen source in shrimp-sensitized rural children in southern China. Allergy. 2017;73(3):585-592. DOI: 10.1111/all.13341

Wang J, Calatroni A, Visness CM, Sampson HA. Correlation of specific IgE to shrimp with cockroach and dust. mite exposure and sensitization in an inner city population. J Allergy Clin Immunol. 2011;128(4):834-837. DOI: 10.1016/j.jaci.2011.07.045

Hoffman DR, Dove DE, Jacobson RS. 140 isolation of four allergens from imported fire ant (solenopsis invicta) venom. J Allergy Clin Immunol. 1988;82(5):818-827. DOI: 10.1016/0091-6749(88)90376-4

Potiwat R, Sitcharungsi R. Ant allergens and hypersensitivity reactions in response to ant stings. Asian Pacific J Allergy Immunol. 2015;33(4):267-275. Disponible en: http://apjai-journal.org/wp-content/uploads/2016/10/2AntallergensAPJAIVol33No4December2015P267.pdf

Farioli L, Losappio LM, Giuffrida MG, Pravettoni V, Micarelli G, Nichelatti M, et al. Mite-induced asthma and IgE levels to shrimp, mite, tropomyosin, arginine kinase, and Der p 10 are the most relevant risk factors for challenge-proven shrimp allergy. Int Arch Allergy Immunol. 2017;174(3-4):133-143. DOI: 10.1159/000481985

Gour N, Lajoie S, Smole U, et al. Dysregulated invertebrate tropomyosin – dectin-1 interaction confers susceptibility to allergic diseases. Sci Immunol. 2018;3(20):pii:eaam9841. DOI: 10.1126/sciimmunol.aam9841

Marrugo J, Hernández L, Villalba V. Prevalence of self-reported food allergy in Cartagena (Colombia) population. Allergol Immunopathol (Madr). 2008;36(6):320-324. DOI: 10.1016/S0301-0546(08)75863-4

Hoyos-Bachiloglu R, Ivanovic-Zuvic D, Álvarez J, Linn K, Thöne N, De-Los-Ángeles PM, et al. Prevalence of parent-reported immediate hypersensitivity food allergy in Chilean school-aged children. Allergol Immunopathol (Madr). 2014;42(6):527-532. DOI: 10.1016/j.aller.2013.09.006

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright (c) 2019 Revista Alergia México

Downloads

Download data is not yet available.