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Graham Roberts Paediatric Allergy and Clinical Immunology,
Department of Paediatrics, Imperial College School of Medicine at St
Mary's, London W2 1NY
Correspondence
to: G Lack gideon.lack{at}sm.stmarys-tr.nthanes.nhs.uk
Allergy to pets, such as cats and dogs, causes significant
morbidity in children.1 Apart from immediate symptoms
of hypersensitivity, allergens from pets are associated with chronic
childhood asthma.
1 2
Clinicians are less familiar with
horse allergy. Our clinical experience suggests that it is an important
problem, even in an urban environment. Despite a lack of obvious
exposure to horse dander this allergen may be responsible for a
child's asthma. We present three of the 28 cases of horse allergy seen
recently in our clinic.
Case 1 Case 2 Case 3 Asthma is an allergic disease of the airways, and allergens have a
key role in the aetiology of the disease as well as being important
triggers of exacerbations.3 Household pets are well known
to cause allergic asthma. A history of past pet ownership, especially
cats, has been found to be related to an increased rate of pet allergy
and asthma.1 Symptoms of asthma and increased bronchial
hyperresponsiveness in childhood are significantly associated with skin
sensitivity to cat dander.4 Cat dander has also been shown
to induce late phase bronchial responses, which are thought to be
important in the pathophysiology of chronic allergic
asthma.
5 6
Much less is known about horse allergy. One
notable textbook on allergy states that "Allergy to horse is now less
of a problem in urban North America than in the early years of this
century. . . ."7 Given that
today we do not rely as much on horses as we did early in the last
century, we would expect horse allergy to be a rare problem in urban
environments, as allergic sensitisation requires chronic or regular
exposure to allergen.8 Our experience, however, suggests
that horse dander is still a major allergen in childhood despite a lack
of regular exposure.
Our cases show how horse dander can play a major part in childhood
asthma within an urban environment. Horse dander may represent a
"hidden" allergen because exposure either is indirect or does not
immediately precede the development of symptoms. A detailed clinical
history is therefore essential for determining the causal allergen.
Peak flow and symptom diaries may be useful in establishing patterns of
disease, which can then be related to indirect exposure to possible
allergens (case 2). Horse allergen seems to be as tenacious as cat
allergen, enabling it to be transferred on clothing.9 Such
carriage probably explains the presence of horse allergen in domestic
dust samples from urban environments.10 Determining the
cause of case 2's symptoms was difficult because the patient presented
with late phase asthmatic symptoms that occurred many hours after
exposure to the allergen.5 In clinical practice, practitioners may be misled into excluding allergy as a cause of
symptoms if they do not immediately follow exposure to an allergen. Case 2 shows how late phase, chronic symptoms may predominate over
acute symptoms where exposure to allergen is chronic or regular.
Skin prick testing is a simple but useful investigation, which often
clarifies the cause of an allergic problem. In case 3, three potential
allergens (nuts, grass pollen, and horse dander) were implicated, and
skin prick testing allowed recognition of the clinically important
allergen. Skin prick testing produces rapid results (15 minutes), is
safe and inexpensive, and has a good sensitivity and reasonable
specificity.11 In the context of a detailed allergy
history, it is a valuable diagnostic tool.
Avoidance of allergens is critical in the management of clinical
allergy and may be sufficient to control symptoms.12
Although it is simple to avoid direct exposure to horses, indirect
exposure can be more difficult (case 2). Appropriate rescue treatment
for accidental exposures comprises an antihistamine and inhaled
Horse allergy is an important paediatric problem even in a young urban
population. It causes a wide range of clinical symptoms from urticaria
to respiratory distress, with both early and late phase respiratory
symptoms. Carriage on clothing allows the aeroallergen access to
the indoor environment, and therefore avoidance is difficult. Horse
allergens that are "hidden" within the indoor enviroment can result
in allergic sensitisation, bronchial inflammation, and chronic asthma.
Successful avoidance may dramatically improve the control of childhood
asthma and reduce the need for steroids.

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Peak expiratory flow in nine year old boy exposed to horse
dander from his sister's riding gear. Lung function deteriorated each
weekend apart from one his sister spent away. Once his sister gave up
riding, variability in peak flow disappeared, with no dips below
200/min
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Case reports
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Case reports
Discussion
References
Within minutes of riding a pony at a
fête, an eight year old boy developed angio-oedema and respiratory
distress. On initial assessment in the accident and emergency
department, he was tachypnoeic with a saturation of 90% in air. He
improved after treatment with oxygen, nebulised salbutamol, intravenous
hydrocortisone, and intravenous chlorpheniramine. Skin prick testing
produced a 6 mm weal to horse dander and a 3 mm weal to house dust mite (positive histamine control, 3 mm). He was advised to avoid horses, to
carry chlorpheniramine in case of accidental exposure, and to use
inhaled salbutamol and intramuscular adrenaline in the event of
respiratory symptoms.
A nine year old boy was referred because of poorly
controlled asthma despite receiving inhaled beclomethasone 400 µg/day. His asthma diary showed dips of more than 50% in his peak
expiratory flow on Friday evenings (figure). These dips persisted all
weekend and were associated with a persistent cough. One concern was
that psychosocial circumstances at home might have accounted for his deterioration at weekends, but this was unfounded. His parents mentioned that he had once had a weekend free of symptoms when his
sister had been away (figure). On Friday evenings his sister went
riding, and she kept her riding gear in their bedroom. Further questioning showed that on direct exposure to horses he experienced rhinitis, conjunctivitis, and wheeze. Skin prick testing with horse
dander produced an 8 mm weal (positive histamine control, 3 mm). His
asthma was controlled once his sister stopped riding. He no longer
requires inhaled steroids.
A five year old boy was referred with asthma.
For two successive summers he had required treatment in the accident and emergency department for wheeze and sneezing, which developed while
walking through fields. On the first occasion he had been eating an ice
cream with nuts. The episodes were thought to be due to either nut
allergy or hay fever. Skin prick testing, however, produced no reaction
to nuts and a small weal (2 mm) to grass pollen (positive control, 4 mm). Closer questioning showed that on both occasions he had come into
close contact with a horse. Skin prick testing to horse dander produced
a 12 mm weal. He was advised to avoid horses and prescribed
chlorpheniramine and a salbutamol inhaler for use if accidentally exposed.
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Discussion
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Case reports
Discussion
References
-agonist for bronchospasm (case 1). Where past exposure has resulted
in life threatening symptoms, children should also have access to a
preloaded adrenaline device (for example, EpiPen, Meridian Medical Technology, St Louis, USA) and should be educated about when and how to
use it. For some children, exposure is unavoidable. In our experience,
these children usually benefit from a combination of prophylactic
treatments: long acting antihistamine and inhaled steroids started one
day before exposure; and inhaled
-agonists used as needed.
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Acknowledgments |
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Contributors: GR and GL participated in writing the paper. GL will act guarantor for the paper.
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Footnotes |
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Funding: GR is supported by a research fellowship from the special trustees at St Mary's Hospital, London.
Competing interests: None declared.
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References |
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Brunekreef B, Groot B, Hoek G.
Pets allergy and respiratory symptoms in children.
Int J Epidemiol
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| 3. | Holgate ST. The cellular and mediator basis of asthma in relation to natural history. Lancet 1997; 350(suppl 11): 5-9[CrossRef][Medline]. |
| 4. | Sears MR, Herbison GP, Holdaway MD, Hewit CJ, Flannery EM, Silva PA. The relative risks of sensitivity to grass pollen, house dust mite and cat dander in the development of childhood asthma. Clin Exp Allergy 1989; 19: 419-424[CrossRef][Medline]. |
| 5. | Warner J. Significance of late reactions after bronchial challenge with house dust mite. Arch Dis Child 1976; 51: 905-911[Abstract]. |
| 6. | Herxheimer H. The late bronchial reaction in induced asthma. Int Arch Allergy Appl Immunol 1952; 3: 323-328[Medline]. |
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| 8. | Sporik R, Holgate ST, Platts-Mills TA, Cogswell JJ. Exposure to house-dust mite allergen (Der p I) and the development of asthma in childhood. A prospective study. N Engl J Med 1990; 323: 502-507[Abstract]. |
| 9. | D'Amato G, Liccardi G, Russo M, Barber D, D'Amato M, Carreira J. Clothing is a carrier of cat allergens. J Allergy Clin Immunol 1997; 99: 577-578[CrossRef][Medline]. |
| 10. | Lind P, Norman PS, Newton M, Lowenstein H, Schwartz B. The prevalence of indoor allergens in the Baltimore area: house dust mite and animal dander antigens measured by immunochemical techniques. J Allergy Clin Immunol 1987; 80: 541-547[CrossRef][Medline]. |
| 11. | Anon. Position paper: allergen and skin tests. The European Academy of Allergology and Clinical Immunology. Allergy 1993; 48(suppl 14): 48-82[Medline]. |
| 12. | Van Velzen E, van den Bos JW, Benckhuijsen JA, van Essel T, de Bruijn R, Aalbers R. Effect of allergen avoidance at high altitude on direct and indirect bronchial hyperresponsiveness and markers of inflammation in children with allergic asthma. Thorax 1996; 51: 582-584[Abstract]. |
(Accepted 13 December 1999)
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