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Allergologie select2024; 8; 51-63; doi: 10.5414/ALX02449E

Animal exposure, sensitization, and allergic symptoms in first-year veterinary medicine students.

Abstract: The AllergoVet study longitudinally examines the influence of animal exposure on the development of sensitization and allergic diseases among veterinary medicine students. In this group, contact to animals usually existed long before the study began. Therefore, the aim of this analysis was to investigate lifelong animal species-specific exposure and the prevalence of sensitizations and allergic symptoms already existing before the start of the study. Questionnaire data, including exposure history, were summarized to determine the duration and intensity of animal-related exposure as well as the prevalence of allergic symptoms to animals. Serologically, specific IgE was determined against ubiquitous inhalant allergens (atopy screen sx1) and against animal allergens using ImmunoCAP. The association between animal-specific sensitization, allergic symptoms, and exposure was analyzed using Fisher's exact test or Cochran-Armitage trend test. All study participants (n = 313) had previous contact with animals, with dogs mentioned most frequently (91.1%) followed by cats (89.5%) and horses (72.2%). Sensitization to ubiquitous allergens (positive sx1 value) was detected in 38.4% of subjects. Approximately 11%, 7%, and 5% were sensitized to cats, dogs, and horses, respectively. Only a small proportion of these sensitizations were associated with self-reported symptoms (41% for cat, 9% for dog, and 13% for horse). While no significant association between animal-specific exposure and sensitization was found for cats and horses, a clear trend emerged for dogs. With increasing duration of exposure to dogs, the number of dog-specific sensitizations decreased significantly (p = 0.0069). Furthermore, a decreasing trend in sx1 sensitization was noted with increasing cat (p = 0.0288) and dog (p = 0.0107) exposure. None of the subjects who grew up on a farm (n = 40) had any sensitization to animals. The sensitization prevalence determined among first-year students in veterinary medicine roughly corresponds to that in the general population. Most animal sensitizations were not clinically relevant. In this collective, a protective effect of increasing exposure to animals in childhood and adolescence was found on sensitization, which was particularly pronounced during contact with dogs.
Publication Date: 2024-03-21 PubMed ID: 38549810PubMed Central: PMC10975734DOI: 10.5414/ALX02449EGoogle Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study investigated how lifelong exposure to different animals affects the development of allergic sensitizations and symptoms in first-year veterinary medicine students.
  • The study found that increased exposure to animals, especially dogs, during childhood and adolescence is associated with a reduced prevalence of allergic sensitization.

Study Objective and Background

  • The research aimed to examine the relationship between animal exposure, allergic sensitization, and allergic symptoms in veterinary students before their formal education began.
  • Since these students typically have extensive contact with animals prior to the study, the focus was on existing sensitizations and symptoms related to different animal species.

Methods

  • Participants: 313 first-year veterinary medicine students.
  • Data Collection:
    • Questionnaires assessing lifelong exposure to animals, including intensity and duration.
    • Self-reported allergic symptoms related to animal exposure.
  • Serological Tests:
    • Measurement of specific IgE antibodies against common inhalant allergens (sx1 panel).
    • Measurement of IgE antibodies specific to animal allergens (cats, dogs, horses) using ImmunoCAP technology.
  • Statistical Analyses:
    • Used Fisher’s exact test and Cochran-Armitage trend test to analyze associations between animal exposure, sensitization, and symptoms.

Key Findings

  • Exposure Patterns:
    • All participants had prior animal contact.
    • Dogs were the most commonly encountered animals (91.1%), followed by cats (89.5%) and horses (72.2%).
  • Prevalence of Sensitization:
    • 38.4% were sensitized to common inhalant allergens in general.
    • 11% were sensitized to cat allergens, 7% to dog allergens, and 5% to horse allergens.
  • Clinical Relevance of Sensitizations:
    • Only a subset of sensitized individuals reported allergic symptoms to the respective animals:
      • 41% for cat sensitization.
      • 9% for dog sensitization.
      • 13% for horse sensitization.
  • Exposure-Sensitization Relationship:
    • No significant link for cats and horses between exposure and sensitization.
    • A significant protective trend for dog exposure:
      • Longer duration of dog exposure correlated with fewer dog-specific sensitizations (p = 0.0069).
      • Similar decreasing trends in overall inhalant sensitization (sx1 panel) were observed with increased dog (p = 0.0107) and cat (p = 0.0288) exposure.
    • None of the students raised on farms (n = 40) showed animal sensitizations, suggesting a strong protective effect related to farm environments.

Conclusions and Implications

  • The prevalence of sensitization in veterinary students was comparable to that in the general population.
  • Most allergic sensitizations detected were not accompanied by symptoms, indicating limited clinical impact at this stage.
  • Higher exposure to animals during childhood and adolescence, especially dogs, appears to have a protective effect against developing sensitization to animal allergens.
  • The results support the idea that early and sustained animal contact might reduce the risk of becoming allergic, which has implications for allergy prevention strategies.

Cite This Article

APA
Zahradnik E, Nöllenheidt C, Sander I, Beine A, Lehnert M, Hoffmeyer F, Raulf M. (2024). Animal exposure, sensitization, and allergic symptoms in first-year veterinary medicine students. Allergol Select, 8, 51-63. https://doi.org/10.5414/ALX02449E

Publication

ISSN: 2512-8957
NlmUniqueID: 101722686
Country: Germany
Language: English
Volume: 8
Pages: 51-63

Researcher Affiliations

Zahradnik, Eva
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Nöllenheidt, Christoph
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Sander, Ingrid
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Beine, Alexandra
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Lehnert, Martin
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Hoffmeyer, Frank
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.
Raulf, Monika
  • Institute for Prevention and Occupational Medicine of the German Social Accident Insurance, Institute of the Ruhr-Universität Bochum (IPA), Bochum, Germany.

Conflict of Interest Statement

All authors declare that no conflict of interest exists. Table 1.Descriptive characteristics of study participants. CharacteristicTotal (n = 313)Females (n = 264)Males (n = 49)p-value*Age, median (range)20 (17-42)20 (17-42)20 (18-33)Current smoker, n (%)43 (13.7)27 (10.2)16 (32.7)0.0002Childhood on farm with animals, n (%)40 (12.8)34 (12.9)6 (12.2)> 0.9999Animal-related education before the veterinary study#, n (%)80 (25.6)64 (24.2)16 (32.7)0.2166Allergic disease** (any), 124 (39.6)106 (40.2)18 (36.7)0.7510   Asthma, n (%)33 (10.5)27 (10.2)6 (12.2)0.6187   Rhinitis, n (%)53 (16.9)44 (16.7)9 (18.4)0.8356   Neurodermatitis, n (%)44 (14.1)40 (15.2)4 (8.2)0.2639   Contact dermatitis, n (%)10 (3.2)9 (3.4)1 (2.0)> 0.9999   Urticaria, n (%)16 (5.1)14 (5.3)2 (4.1)> 0.9999   Food allergy, n (%)30 (9.6)28 (10.6)2 (4.1)0.1929   Insect allergy, n (%)9 (2.9)8 (3.0)1 (2.0)> 0.9999Allergic symptoms to animals*** (any)30 (9.6)24 (9.1)6 (12.2)0.4391   Cat, n (%)23 (7.3)20 (7.6)3 (6.1)> 0.9999   Dog, n (%)7 (2.2)5 (1.9)2 (4.1)0.3015   Horse, n (%)7 (2.2)5 (1.9)2 (4.1)0.3015   Small mammals#, n (%)6 (1.9)5 (1.9)1 (2.0)> 0.9999   Others (birds), n (%)3 (1.0)2 (0.8)1 (2.0)0.4010Previous contact to animals (any)313 (100)   Cat, n (%)280 (89.5)239 (90.5)41 (83.7)0.2010   Dog, n (%)285 (91.1)242 (91.7)43 (87.8)0.4118   Horse, n (%)226 (72.2)207 (78.4)19 (38.8)< 0.0001   Small mammals&, n (%)275 (87.9)238 (90.2)37 (75.5)0.0077   Others (non-mammals)§, n (%)210 (67.1)175 (66.3)35 (71.4)0.5133   Farm animals$, n (%)164 (52.4)136 (51.5)28 (57.1)0.5344Current pet ownership (any)115 (36.7)99 (37.5)16 (32.7)0.6288   Cat, n (%)51 (16.3)49 (18.6)2 (4.1)0.0103   Dog, n (%)63 (20.1)54 (20.5)9 (18.4)0.8475   Small mammals&, n (%)28 (8.9)26 (9.8)2 (4.1)0.2773   Others (non-mammals)§, n (%)27 (8.6)20 (7.6)7 (14.3)0.1606*Females vs. males, Fisher’s exact test; **doctor’s diagnosis; ***self-reported symptoms; #veterinary technicians, animal caretaker, farmer, biologist, veterinary technical assistant, animal healer, hoof orthopedist, equine ostheopath, butcher; &rabbit, guinea pig, hamster, gerbil, mouse, rat, chinchilla, ferret, degus, marten, hedgehog; §birds (incl. poultry), fish, reptiles; $cattle, pig, goat, sheep. Bold = significantly different frequencies. Table 2.Total and specific IgE antibodies. Total (n = 313)Females (n = 264)Males (n = 49)p-value*Total IgE > 100 kU/Ln (%)83 (26.5%)68 (25.8%)15 (30.6%)0.484IgE kU/L 218 (103 – 3,436)220 (103 – 3,436)168 (110 – 492)sx1 positivesn (%)120 (38.4%)92 (34.8%)28 (57.1%)0.004sIgE kU/L 8.64 (0.36 – 883)8.63 (0.36 – 883)9.80 (0.39 – 54.2)HDM positivesn (%)76 (24.3%)59 (22.3%)17 (34.7%)0.071sIgE kU/L9.34 (0.36 – 518)8.39 (0.36 – 518)11.6 (0.40 – 20.4)Cat positivesn (%)34 (10.9%)29 (11.0%)5 (10.2%)>0.999sIgE kU/L1.65 (0.36 – 244)1.97 (0.36 – 244)0.72 (0.58 – 7.52)Dog positivesn (%)22 (7.0%)18 (6.8%)4 (8.2%)0.760sIgE kU/L0.98 (0.36 – 8.72)0.98 (0.36 – 8.72)0.98 (0.43 – 3.34)Horse positivesn (%)16 (5.1%)15 (5.7%)1 (2.0%)0.482sIgE kU/L0.59 (0.36 – 7.73)0.56 (0.36 – 7.73)1.93Cattle positivesn (%)8 (2.6%)5 (1.9%)3 (6.1%)0.114sIgE kU/L0.55 (0.36 – 1.79)0.50 (0.36 – 1.20)1.01 (0.45 – 1.06)IgE concentrations in kU/L are presented as median with range. *Females vs. males, Fisher’s exact test. sIgE = specific IgE; HDM = house dust mite. Bold = significantly different frequencies. Figure 1.Sensitization profile of 47 individuals with specific IgE reactivity to animals. A) Distribution of CAP-classes. B) Number of animal sensitizations. C) Distribution of mono- and poly-sensitizations.Figure 2.Distribution of single allergen components in subjects with sensitization to cat (A), dog (B), and horse (C).Figure 3.Relationship between sensitization and self-reported allergic symptoms to cats (A), dogs (B), and horses (C).Figure 4.Specific IgE levels (A, B, C) and the proportion of specific IgE to total IgE (D, E, F) in subjects sensitized to cats (A and D), dogs (B and E), and horses (C and F). The vertical solid lines represent medians, and the dashed lines show the IgE cut-off value of 0.35 kU/L. Statistical significance was tested using the Mann-Whitney test.Figure 5.Relationship between sensitization and categories of life-time exposure to cats (A), dogs (B), and horses (C).

References

This article includes 50 references
  1. Linneberg A, Gislum M, Johansen N, Husemoen LLN, Jørgensen T. Temporal trends of aeroallergen sensitization over twenty-five years.. Clin Exp Allergy 2007; 37: 1137–1142.
    pubmed: 17651142
  2. Warm K, Lindberg A, Lundbäck B, Rönmark E. Increase in sensitization to common airborne allergens among adults – two population-based studies 15 years apart.. Allergy Asthma Clin Immunol 2013; 9: 20.
    pmc: PMC3684537pubmed: 23758681
  3. Kölli F, Breyer M-K, Hartl S, Burghuber O, Wouters EFM, Sigsgaard T, Pohl W, Kohlböck G, Breyer-Kohansal R. Aero-Allergen Sensitization in the General Population: Longitudinal Analyses of the LEAD (Lung Heart Social Body) Study.. J Asthma Allergy 2022; 15: 461–473.
    pmc: PMC9012316pubmed: 35431559
  4. Zahradnik E, Raulf M. Respiratory Allergens from Furred Mammals: Environmental and Occupational Exposure.. Vet Sci 2017; 4: 4.
    pmc: PMC5644656pubmed: 29056697
  5. Bonini S, Buonacucina A. Occupational Hazards in Veterinarians: An Updating.. J Veterinar Sci Technol 2015; 07.
  6. Hoffmeyer F, Beine A, Lotz A, Kleinmüller O, Nöllenheidt C, Zahradnik E, Nienhaus A, Raulf M. Upper and lower respiratory airway complaints among female veterinary staff.. Int Arch Occup Environ Health 2022; 95: 665–675.
    pmc: PMC8938376pubmed: 34669024
  7. Fowler HN, Holzbauer SM, Smith KE, Scheftel JM. Survey of occupational hazards in Minnesota veterinary practices in 2012.. J Am Vet Med Assoc 2016; 248: 207–218.
    pmc: PMC5710733pubmed: 26720089
  8. Samadi S, Wouters IM, Heederik DJJ. A review of bio-aerosol exposures and associated health effects in veterinary practice.. Ann Agric Environ Med 2013; 20: 206–221.
    pubmed: 23772565
  9. Susitaival P, Kirk JH, Schenker MB. Atopic symptoms among California veterinarians.. Am J Ind Med 2003; 44: 166–171.
    pubmed: 12874849
  10. Samadi S, Spithoven J, Jamshidifard A-R, Berends BR, Lipman L, Heederik DJJ, Wouters IM. Allergy among veterinary medicine students in The Netherlands.. Occup Environ Med 2012; 69: 48–55.
    pubmed: 21632519
  11. Lehnert M, Beine A, Hoffmeyer F, Taeger D, Brüning T, Raulf M. Self-Reported Survey on Allergy Symptoms Among First-Year Students in Veterinary Medicine: A Preamble to the AllergoVet Cohort Study.. Adv Exp Med Biol 2020; 1279: 9–14.
    pubmed: 32170668
  12. Hoffmeyer F, Beine A, Lehnert M, Berresheim H, Taeger D, van Kampen V, Sander I, Zahradnik E, Brüning T, Raulf M. The Pattern of Sensitization Influences Exhaled and Nasal Nitric Oxide Levels in Young Adults.. Adv Exp Med Biol 2020; 1279: 15–26.
    pubmed: 32193864
  13. Heinzerling LM, Burbach GJ, Edenharter G, Bachert C, Bindslev-Jensen C, Bonini S, Bousquet J, Bousquet-Rouanet L, Bousquet PJ, Bresciani M, Bruno A, Burney P, Canonica GW, Darsow U, Demoly P, Durham S, Fokkens WJ, Giavi S, Gjomarkaj M, Gramiccioni C. GA(2)LEN skin test study I: GA(2)LEN harmonization of skin prick testing: novel sensitization patterns for inhalant allergens in Europe.. Allergy 2009; 64: 1498–1506.
    pubmed: 19772515
  14. Bousquet P-J, Chinn S, Janson C, Kogevinas M, Burney P, Jarvis D. Geographical variation in the prevalence of positive skin tests to environmental aeroallergens in the European Community Respiratory Health Survey I.. Allergy 2007; 62: 301–309.
    pubmed: 17298348
  15. Schmitz R, Ellert U, Kalcklösch M, Dahm S, Thamm M. Patterns of sensitization to inhalant and food allergens - findings from the German Health Interview and Examination Survey for Children and Adolescents.. Int Arch Allergy Immunol 2013; 162: 263–270.
    pubmed: 24022179
  16. Asarnoj A, Hamsten C, Wadén K, Lupinek C, Andersson N, Kull I, Curin M, Anto J, Bousquet J, Valenta R, Wickman M, van Hage M. Sensitization to cat and dog allergen molecules in childhood and prediction of symptoms of cat and dog allergy in adolescence: A BAMSE/MeDALL study.. J Allergy Clin Immunol 2016; 137: 813–821.
    pmc: PMC6597346pubmed: 26686472
  17. Rönmark E, Warm K, Bjerg A, Backman H, Hedman L, Lundbäck B. High incidence and persistence of airborne allergen sensitization up to age 19 years.. Allergy 2017; 72: 723–730.
    pubmed: 27659134
  18. Melén E, Bergström A, Kull I, Almqvist C, Andersson N, Asarnoj A, Borres MP, Georgellis A, Pershagen G, Westman M, van Hage M, Ballardini N. Male sex is strongly associated with IgE-sensitization to airborne but not food allergens: results up to age 24 years from the BAMSE birth cohort.. Clin Transl Allergy 2020; 10: 15.
    pmc: PMC7247167pubmed: 32489587
  19. Haftenberger M, Laußmann D, Ellert U, Kalcklösch M, Langen U, Schlaud M, Schmitz R, Thamm M. Prävalenz von Sensibilisierungen gegen Inhalations- und Nahrungsmittelallergene : Ergebnisse der Studie zur Gesundheit Erwachsener in Deutschland (DEGS1).. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2013; 56: 687–697.
    pubmed: 23703487
  20. Hemmer W, Sestak-Greinecker G, Braunsteiner T, Wantke F, Wöhrl S. Molecular sensitization patterns in animal allergy: Relationship with clinical relevance and pet ownership.. Allergy 2021; 76: 3687–3696.
    pubmed: 33914361
  21. Bjerg A, Winberg A, Berthold M, Mattsson L, Borres MP, Rönmark E. A population-based study of animal component sensitization, asthma, and rhinitis in schoolchildren.. Pediatr Allergy Immunol 2015; 26: 557–563.
    pubmed: 26059105
  22. Konradsen JR, Nordlund B, Onell A, Borres MP, Grönlund H, Hedlin G. Severe childhood asthma and allergy to furry animals: refined assessment using molecular-based allergy diagnostics.. Pediatr Allergy Immunol 2014; 25: 187–192.
    pubmed: 24460778
  23. Roger A, Lazo C, Arias N, Quirant B, Albert N, Gómez M, Schayman W. Using Component-Resolved Diagnosis to Characterize the Sensitization to Specific Cat and Dog Allergens in Patients with Allergic Respiratory Diseases in Catalonia, Spain.. Int Arch Allergy Immunol 2023; 184: 440–446.
    pmc: PMC10906471pubmed: 36657403
  24. Liccardi G, Asero R, D’Amato M, D’Amato G. Role of sensitization to mammalian serum albumin in allergic disease.. Curr Allergy Asthma Rep 2011; 11: 421–426.
    pubmed: 21809117
  25. Huang Z, Zhu H, Lin R, Wu L, An N, Zheng P, Sun B. Serum Albumin as a Cross-Reactive Component in Furry Animals May Be Related to the Allergic Symptoms of Patients with Rhinitis.. J Asthma Allergy 2021; 14: 1231–1242.
    pmc: PMC8544268pubmed: 34707374
  26. Apostolovic D, Sánchez-Vidaurre S, Waden K, Curin M, Grundström J, Gafvelin G, Cirkovic Velickovic T, Grönlund H, Thomas WR, Valenta R, Hamsten C, van Hage M. The cat lipocalin Fel d 7 and its cross-reactivity with the dog lipocalin Can f 1.. Allergy 2016; 71: 1490–1495.
    pubmed: 27289080
  27. Hilger C, Swiontek K, Arumugam K, Lehners C, Hentges F. Identification of a new major dog allergen highly cross-reactive with Fel d 4 in a population of cat- and dog-sensitized patients.. J Allergy Clin Immunol 2012; 129: 1149–1151.
    pubmed: 22104604
  28. Nilsson OB, Binnmyr J, Zoltowska A, Saarne T, van Hage M, Grönlund H. Characterization of the dog lipocalin allergen Can f 6: the role in cross-reactivity with cat and horse.. Allergy 2012; 67: 751–757.
    pubmed: 22515174
  29. Dávila I, Domínguez-Ortega J, Navarro-Pulido A, Alonso A, Antolín-Amerigo D, González-Mancebo E, Martín-García C, Núñez-Acevedo B, Prior N, Reche M, Rosado A, Ruiz-Hornillos J, Sánchez MC, Torrecillas M. Consensus document on dog and cat allergy.. Allergy 2018; 73: 1206–1222.
    pubmed: 29318625
  30. Burbach GJ, Heinzerling LM, Edenharter G, Bachert C, Bindslev-Jensen C, Bonini S, Bousquet J, Bousquet-Rouanet L, Bousquet PJ, Bresciani M, Bruno A, Canonica GW, Darsow U, Demoly P, Durham S, Fokkens WJ, Giavi S, Gjomarkaj M, Gramiccioni C, Haahtela T. GA(2)LEN skin test study II: clinical relevance of inhalant allergen sensitizations in Europe.. Allergy 2009; 64: 1507–1515.
    pubmed: 19772516
  31. Sánchez A, Cardona R, Munera M, Calvo V, Tejada-Giraldo M, Sánchez J. Nasal Provocation Test with Cat and Dog Extracts: Results according to Molecular Components. Pulm Med 2020; 2020: 6365314.
    pmc: PMC7001676pubmed: 32047667
  32. Käck U, Asarnoj A, Grönlund H, Borres MP, van Hage M, Lilja G, Konradsen JR. Molecular allergy diagnostics refine characterization of children sensitized to dog dander. J Allergy Clin Immunol 2018; 142: 1113–1120.
    pubmed: 29852259
  33. Simpson A, Custovic A. Pets and the development of allergic sensitization. Curr Allergy Asthma Rep 2005; 5: 212–220.
    pubmed: 15842959
  34. Chen C-M, Tischer C, Schnappinger M, Heinrich J. The role of cats and dogs in asthma and allergy--a systematic review. Int J Hyg Environ Health 2010; 213: 1–31.
    pubmed: 20053584
  35. Lødrup Carlsen KC, Roll S, Carlsen K-H, Mowinckel P, Wijga AH, Brunekreef B, Torrent M, Roberts G, Arshad SH, Kull I, Krämer U, von Berg A, Eller E, Høst A, Kuehni C, Spycher B, Sunyer J, Chen C-M, Reich A, Asarnoj A. Does pet ownership in infancy lead to asthma or allergy at school age? Pooled analysis of individual participant data from 11 European birth cohorts. PLoS One 2012; 7: e43214.
    pmc: PMC3430634pubmed: 22952649
  36. Pinot de Moira A, Strandberg-Larsen K, Bishop T, Pedersen M, Avraam D, Cadman T, Calas L, Casas M, de Lauzon Guillain B, Elhakeem A, Esplugues A, Estarlich M, Foong RE, Haakma S, Harris JR, Huang R-C, Inskip H, Lertxundi A, Mensink-Bout SM, Nader JLT. Associations of early-life pet ownership with asthma and allergic sensitization: A meta-analysis of more than 77,000 children from the EU Child Cohort Network. J Allergy Clin Immunol 2022; 150: 82–92.
    pubmed: 35150722
  37. Bjerg A, Ekerljung L, Eriksson J, Näslund J, Sjölander S, Rönmark E, Dahl Å, Holmberg K, Wennergren G, Torén K, Borres MP, Lötvall J, Lundbäck B. Increase in pollen sensitization in Swedish adults and protective effect of keeping animals in childhood. Clin Exp Allergy 2016; 46: 1328–1336.
    pubmed: 27159904
  38. Taniguchi Y, Kobayashi M. Exposure to dogs and cats and risk of asthma: A retrospective study. PLoS One 2023; 18: e0282184.
    pmc: PMC9994694pubmed: 36888591
  39. Hesselmar B, Hicke-Roberts A, Lundell A-C, Adlerberth I, Rudin A, Saalman R, Wennergren G, Wold AE. Pet-keeping in early life reduces the risk of allergy in a dose-dependent fashion. PLoS One 2018; 13: e0208472.
    pmc: PMC6300190pubmed: 30566481
  40. Hesselmar B, Aberg B, Eriksson B, Björkstén B, Aberg N. High-dose exposure to cat is associated with clinical tolerance – -a modified Th2 immune response?. Clin Exp Allergy 2003; 33: 1681–1685.
    pubmed: 14656355
  41. Heinrich J, Gehring U, Douwes J, Koch A, Fahlbusch B, Bischof W, Wichmann HE. Pets and vermin are associated with high endotoxin levels in house dust. Clin Exp Allergy 2001; 31: 1839–1845.
    pubmed: 11737034
  42. Fuertes E, Standl M, Markevych I, Bischof W, Heinrich J. Is the association between pet ownership and indoor endotoxin levels confounded or modified by outdoor residential greenspace?. Sci Total Environ 2018; 625: 716–721.
    pubmed: 29306159
  43. Schuijs MJ, Willart MA, Vergote K, Gras D, Deswarte K, Ege MJ, Madeira FB, Beyaert R, van Loo G, Bracher F, von Mutius E, Chanez P, Lambrecht BN, Hammad H. Farm dust and endotoxin protect against allergy through A20 induction in lung epithelial cells. Science 2015; 349: 1106–1110.
    pubmed: 26339029
  44. Gómez-Gallego C, Forsgren M, Selma-Royo M, Nermes M, Collado MC, Salminen S, Beasley S, Isolauri E. The Composition and Diversity of the Gut Microbiota in Children Is Modifiable by the Household Dogs: Impact of a Canine-Specific Probiotic. Microorganisms 2021; 9: 9.
    pmc: PMC8001081pubmed: 33800493
  45. Song SJ, Lauber C, Costello EK, Lozupone CA, Humphrey G, Berg-Lyons D, Caporaso JG, Knights D, Clemente JC, Nakielny S, Gordon JI, Fierer N, Knight R. Cohabiting family members share microbiota with one another and with their dogs. eLife 2013; 2: e00458.
    pmc: PMC3628085pubmed: 23599893
  46. Tun HM, Konya T, Takaro TK, Brook JR, Chari R, Field CJ, Guttman DS, Becker AB, Mandhane PJ, Turvey SE, Subbarao P, Sears MR, Scott JA, Kozyrskyj AL. Exposure to household furry pets influences the gut microbiota of infant at 3-4 months following various birth scenarios.. Microbiome 2017; 5: 40.
    pmc: PMC5382463pubmed: 28381231
  47. Rooks MG, Garrett WS. Gut microbiota, metabolites and host immunity.. Nat Rev Immunol 2016; 16: 341–352.
    pmc: PMC5541232pubmed: 27231050
  48. Wlasiuk G, Vercelli D. The farm effect, or: when, what and how a farming environment protects from asthma and allergic disease.. Curr Opin Allergy Clin Immunol 2012; 12: 461–466.
    pubmed: 22892709
  49. Campbell BE, Lodge CJ, Lowe AJ, Burgess JA, Matheson MC, Dharmage SC. Exposure to ‘farming’ and objective markers of atopy: a systematic review and meta-analysis.. Clin Exp Allergy 2015; 45: 744–757.
    pubmed: 25270644
  50. Eller E, Roll S, Chen C-M, Herbarth O, Wichmann H-E, von Berg A, Krämer U, Mommers M, Thijs C, Wijga A, Brunekreef B, Fantini MP, Bravi F, Forastiere F, Porta D, Sunyer J, Torrent M, Høst A, Halken S, Lødrup Carlsen KC. Meta-analysis of determinants for pet ownership in 12 European birth cohorts on asthma and allergies: a GA2LEN initiative.. Allergy 2008; 63: 1491–1498.
    pubmed: 18721248

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