- Open Access
A prospective study on insect bite hypersensitivity in horses exported from Iceland into Switzerland
- Sigurbjörg Torsteinsdottir†1,
- Stephan Scheidegger†2, 3,
- Silvia Baselgia2,
- Sigridur Jonsdottir1, 2,
- Vilhjalmur Svansson1,
- Sigridur Björnsdottir4 and
- Eliane Marti2Email authorView ORCID ID profile
© The Author(s) 2018
- Received: 15 May 2018
- Accepted: 28 October 2018
- Published: 3 November 2018
Insect bite hypersensitivity (IBH) is an IgE-mediated dermatitis caused by bites of Culicoides spp., which occurs frequently in horses imported from Iceland to continental Europe. IBH does not occur in Iceland because Culicoides species that bite horses are not present. However, Simulium vittatum (S. vittatum) are found in Iceland. In Europe, blood basophils from IBH-affected horses release significantly more sulfidoleukotrienes (sLT) than those from healthy controls after in vitro stimulation with Culicoides nubeculosus (C. nubeculosus) and S. vittatum. Aims of the study were: (I) using the sLT release assay, to test if horses living in Iceland were sensitized to S. vittatum and (II) to determine in a longitudinal study in horses imported from Iceland to Switzerland whether the sLT release assay would allow to predict which horses would develop IBH.
Horses in Iceland, even when living in high S. vittatum areas, were usually not sensitized to S. vittatum or C. nubeculosus. Incidence of IBH in the 145 horses from the longitudinal study was 51% and mean time until IBH developed was 2.5 ± 1 year. Before import and after the first summer following import, there were no significant differences in sLT release between the endpoint healthy (H) and IBH groups. After the 2nd summer, when the number of clinically affected horses increased in the endpoint IBH group, a significantly higher sLT release after stimulation with C. nubeculosus but not with S. vittatum was observed. After the 3rd and 4th summer, the endpoint IBH group had a significantly higher sLT release with C. nubeculosus and S. vittatum than the endpoint H group. Some of the horses that remained healthy became transiently positive in the sLT release assay upon stimulation of their peripheral blood leucocytes with C. nubeculosus.
Horses in Iceland are not sensitized to S. vittatum. In horses that develop IBH, sensitization to S. vittatum is secondary to sensitization to C. nubeculosus and probably a result of an immunological cross-reactivity. A sLT release assay cannot be used to predict which horses will develop IBH. A transient positive reaction in the sLT release assay observed in horses that remained healthy suggests that immunoregulatory mechanisms may control an initial sensitization of the healthy horses.
- Icelandic horses
- Insect bite hypersensitivity
- Sulfidoleukotriene release assay
Insect bite hypersensitivity (IBH) in horses also known as summer eczema (SE), sweet-itch, Queensland itch, Kasen or Culicoides hypersensitivity, is a chronic, recurrent seasonal dermatitis of horses caused by an allergic reaction to the bite of midges, Culicoides spp. (reviewed in ). IBH affected horses were also reported to react against other blood feeding insects like black flies (Simulium spp.), stable flies (Stomoxys calcitrans), mosquitoes and horseflies [2–4].
Several studies have shown that IBH is an IgE-mediated, type I hypersensitivity reaction . Horses with IBH but only rarely healthy control horses, have serum IgE antibodies against salivary gland proteins of Culicoides spp. [15–20]. Furthermore, in vitro stimulation of peripheral blood leucocytes (PBL) with Culicoides spp. allergens leads to the release of histamine or sulphidoleukotrienes (sLT) in IBH-affected but only rarely in healthy control horses [21–23]. The value of a sLT release assay, with Culicoides nubeculosus (C. nubeculosus) as allergen, for in vitro diagnosis of IBH has been evaluated in a well characterised, large population of IBH-affected and healthy animals and was shown to have a sensitivity of 80% and a specificity of 97% . This study had also shown that horses with IBH are often not only sensitized to C. nubeculosus but also to S. vittatum . These horses also have IgE antibodies binding to salivary gland allergens of both C. nubeculosus and S. vittatum  and at least one of the S. vittatum allergens is cross-reactive with the corresponding allergen from C. nubeculosus . These findings raised the question whether horses living in Iceland could be sensitized to S. vittatum allergens, as these black flies are present in Iceland and bite horses, and whether horses sensitized to black flies in Iceland would be more prone to develop IBH after importation to Culicoides-rich environments, like Switzerland.
The aims of our study were (I) to test whether horses living in Iceland were sensitized to S. vittatum allergens by using the in vitro sLT release test and (II) to determine in a longitudinal study of horses imported from Iceland to Switzerland, whether the in vitro sLT release assay with C. nubeculosus and S. vittatum allergen extracts would allow any prediction whether horses would develop IBH.
Design of the study
Data was collected in the years 2000–2010 from 275 horses of the Icelandic breed all born in Iceland, of which 130 remained in Iceland and 145 were exported to Switzerland. The exported horses were monitored at the end of every summer after import for occurrence of clinical signs of IBH over a period of one to up to six summers. The horses classified as remaining healthy (H) had to have been exposed to Culicoides spp. for at least three summers. Seventy-two of the 145 imported horses arrived in winter (out of IBH season, defined as 1st of October until 31st of April) when the adult insects causing IBH are not present in Switzerland, while the remaining 73 horses were imported during the IBH season. A clinical examination was performed once a year at the end of each summer, blood samples were taken and the clinical history was recorded. Furthermore, in 40 of these horses, clinical examination and blood sampling had already been performed in Iceland before export. At the end of the study the clinical status towards IBH (healthy/IBH/unknown) was determined.
The group of horses remaining in Iceland consisted of 91 males and 39 females with an average age of 9.5 years (range 3–25 years). Out of these 130 horses, 76 were from infested black fly areas and 54 from areas with low exposure. The group of exported horses (n = 145) consisted of 111 males and 34 females. After import the horses lived in many different stables with other Icelandic horses in Switzerland. The age of the horses at the time of export was 4–12 years.
All horses were classified at the end of each IBH season as IBH-affected, not affected with IBH (healthy) or unknown diagnosis when the clinical signs and history did not allow a determination of whether the horse had IBH or not. This was for example the case when horses had mild pruritus and were immediately treated locally with repellents or anti-inflammatory ointments and thus had no clinical signs of IBH at the time of examination.
IBH-affected horses had pruritus with scratching and scaling, excoriations and thickening of the skin along the dorsal midline, mainly at the base of the mane and tail. Sometimes the ventral midline and/or the head were affected too. When clinical signs occurred for the first time, the diagnosis was confirmed retrospectively after remission of clinical signs in winter and recurrence of the disease the next summer. Following clinical diagnosis of IBH all horses received a wide variety of treatments such as sweet itch blankets, local application of various lotions for insect and pruritus control and in few cases systemic application of the corticosteroid triamcinoloni acedonidum (Kenacort®). Some of the IBH-affected horses were kept in the stable most of the day or were not allowed access to pasture during the IBH season.
The H horses had no clinical signs of scratching or skin alteration and were not treated against IBH. After import, all horses were vaccinated against tetanus and equine influenza and dewormed regularly.
Blood samples from the horses remaining in Iceland were obtained in August, when S. vittatum are active in Iceland. The horses in Switzerland were sampled at the end of each summer and 40 of them also before export. Sampling was done by jugular venipuncture into ACD-B vacuette tubes (Greiner Bio-One vacuette GmbH, St-Gallen, Switzerland). Blood samples were kept at 10–25 °C and the sLT release assay (see below) performed within 24 h.
The horses remaining in Iceland had no clinical signs of IBH.
Horses exported to Switzerland and assigned to the H endpoint group had not shown clinical signs of IBH at any time of the follow up study and had to be free of IBH at least three summers after import from Iceland, even though living in an environment where IBH-affected horses were living (i.e. as marker for the presence of Culicoides spp.). These horses had not been subjected to prophylactic treatments against IBH (for example blankets etc.).
In 21 horses the clinical outcome was not clear enough to assign them to the healthy or IBH-endpoint group. This was the case when they were treated against IBH (blanket, repellents, etc.) as soon as they were slightly itchy or had crusts at the base of the mane and tail and the owners did not want to stop this treatment to see whether clinical signs of IBH would develop.
Horses assigned to the IBH endpoint group had shown the typical clinical signs of IBH, which recurred the next summer after remission in winter.
In vitro sulfidoleukotriene (sLT) release assay
The Equine CAST® (Cellular Antigen Stimulation Test; Bühlmann Laboratories AG Schönenbuch, Switzerland) was performed as previously described . Briefly: allergen extracts were made from frozen insects (whole body) . C. nubeculosus were laboratory bred, while S. vittatum had been collected in Iceland. The C. nubeculosus extract was used at a final concentration of 2 μg/mL and the S. vittatum extract was used at a final concentration of 10 μg/mL .
The leukocyte rich plasma from the blood samples was collected, transferred into a tube and centrifuged at 130×g for 10 min at RT. The supernatant containing 90% of the platelets was removed and the pelleted cells were resuspended in 1 mL stimulation buffer (Bühlmann Laboratories AG) per 9 mL of ACD-B anticoagulated blood. Cell stimulation was performed following the manufacturer’s instruction, either without stimulation to determine the spontaneous sLT release, or stimulation with Concanavalin A (20 μg/mL) as a control or with the C. nubeculosus and S. vittatum extracts. After 40 min incubation at 37 °C the supernatants were removed and kept frozen for maximum 1 month until further processing. sLT determination was carried out following the manufacturer’s instructions using the Equine CAST® ELISA (Bühlmann Laboratories AG). For all further evaluations the values of the net stimulation were used, i.e. the spontaneous sLT release was subtracted from the values obtained with Concanavalin A or with the allergen extracts. Horses with sLT release < 250 pg/mL with Concanavalin A were classified as ‘non responders’ (NR) [4, 21]. In the 1st year, 6 out of the 126 horses tested in the CAST® were classified as NR, in the 2nd year 2 out of 111, in the 3rd year 6 out of 85 and in the 4th year, 9 out of 60. The CAST results with the insect extracts of NR horses were not included in the statistical analyses.
To distinguish between positive or negative test results the cut-off values determined previously  were used. For the C. nubeculosus stimulation, the cut-off was 310 pg/mL and for S. vittatum 200 pg/mL.
Statistical analyses were carried out with the statistical software package NCSS 2011 (NCSS, Kaysville, Utah 84037, USA). A preliminary analysis indicated that the releases of sLT (pg/mL) were not distributed normally, even after logarithmic transformation. Medians and ranges were used subsequently for descriptive purposes.
To compare sLT release in the horses in Iceland living in a high or a low Simulium infested area, a Mann–Whitney U-test was performed.
With the 112 horses in Switzerland with a clear clinical endpoint (H or IBH) at the end of the study, we analyzed whether gender and season of import (2-tailed Fisher’s exact test), age at import, and number of summers and months until the horses developed IBH (two sample T-test) were associated with clinical disease.
The nonparametric Mann–Whitney U-test was used to compare continuous variables such as released sLT after stimulation with Concanavalin A, S. vittatum or C. nubeculosus whole body extract in IBH-affected and healthy horses.
To compare binary variables such as number of IBH-affected and healthy horses with sLT levels above or below the cut-offs defined above, the 2-tailed Fisher’s exact test was used.
The clinical diagnosis and CAST results with the insect extracts were available at all time points over a period of at least four summers in 29 endpoint H and 27 endpoint IBH horses. In order to investigate whether the CAST with the allergen extracts would allow identification of IBH prone horses before they develop clinical signs of the disease, the data were analyzed as follows: The summer when IBH-affected horses developed clinical signs of IBH for the first time was defined as T0 and the previous summers when the respective horses were exposed to insect bites but did not show clinical signs of IBH were set as T − 1, T − 2, T − 3 etc. The years following the first summer with IBH were defined as T + 1, T + 2 etc. In the horses that remained healthy until the end of the study, i.e. over four summers, T0 was defined as the last year of the study and T − 1, T − 2, T − 3 as the respective preceding summers. The percentage of horses giving a positive test results with C. nubeculosus or S. vittatum antigen extracts at the different time points was then compared between the groups of horses that remained healthy or developed IBH. The two tailed Fisher’s exact test was used to determine whether there was a significant difference in the proportion of horses giving a positive test result between both groups.
sLT release from C. nubeculosus and S. vittatum-stimulated peripheral blood leukocytes of horses remaining in Iceland
Sulfidoleukotriene (sLT) production by peripheral blood leucocytes (PBL) from horses remaining in Iceland in areas with low or high infestation with Simulium vittatum
Incubation of PBL with
Median (range) of sLT released (pg/mL) from PBL of horses coming from areas with
Low versus high
Low Simulium (N = 53)
High Simulium (N = 75)
Development of clinical signs of IBH in horses imported from Iceland to Switzerland
Number of horses involved in the longitudinal study before export from Iceland and one (T − 1), two (T − 2), three (T − 3) and four (T − 4) summers after importation from Iceland into Switzerland
Clinical status at time point
Tested in CAST
Horses that remained healthy
Horses that developed IBHa
Factors influencing the clinical endpoint
From the 112 imported horses exposed for at least three summers to Culicoides spp., 55 horses (49%) had remained healthy and 57 (51%) had developed IBH. With these horses, we analyzed whether gender, age at import and season of import could influence the clinical endpoint. Furthermore, we also determined the mean numbers of summers and months following import until the horses developed IBH.
Factors influencing the clinical endpoint in 55 horses that remained healthy (H) and 57 horses that developed insect bite hypersensitivity (IBH)
H (n = 55)
IBH (n = 57)
Age at import (mean year ± SD)
7.1 ± 1.55
7.5 ± 1.61
Import during the IBH season (N/%)
Import out of the IBH season (N/ %)
Mean number ± SD of summers since import until clinical outcomea
3.6 ± 0.8
2.8 ± 1
Mean number ± SD of months since import until clinical outcomea
39 ± 10
30 ± 12
Time course of CAST results in relation to clinical endpoint
Median (range) sLT release (pg/mL) after incubation of peripheral blood leukocytes (PBL) with C. nubeculosus extract (Cul2: 2 μg/mL) or S. vittatum extract (Sim10: 10 μg/mL) from horses that remained healthy (H) or developed insect bite hypersensitivity (IBH) at different time points (see Table 2 for number of horses included at each time point)
Incubation of PBL with
Median (range) of sLT released (pg/mL) from horses with clinical endpoint
H versus IBH
T − 1
T − 2
T − 3
T − 4
Predictive value of the sLT release assay for the identification of IBH susceptible horses before first clinical signs of IBH
In order to assess if the CAST could allow to predict whether a horse would develop IBH before outbreak of the clinical signs, horses were grouped in those that developed IBH and those that remained healthy and the year when the first signs of IBH occurred was set as T0 while the preceding years were set as T − 1, T − 2 etc.
Horses imported from Iceland to continental Europe represent a unique model to study the natural course of IBH because of the absence of Culicoides in Iceland and the high prevalence of this disease following import to an environment where Culicoides are present. One of the major difficulties of the study was that the horses were privately owned and living in different stables all over Switzerland. We tried to control for exposure to Culicoides spp. by only including horses living where exposure to Culicoides spp. was known to occur, by using the presence of other IBH-affected horses. The severity of IBH was not evaluated because horses were often treated at first clinical signs. Severe IBH cases were thus rare. The horses in Iceland showed no clinical signs of IBH and after the first summer in Switzerland, only two confirmed cases of IBH out of the 145 horses were found. The prevalence then increased to up to 50% in the fourth summer following import, similarly to what has been found previously . Although only 30% of the horses had a confirmed diagnosis of IBH after the third summer, we speculate that the real incidence was already higher at that time point because in 20% of the horses the diagnosis was not clear and thus only 50% of the horses were definitely free of IBH. The mean time until onset of IBH following import was 2.5 years and comparable to what has been described [6, 26]. In accordance with a previous study , the incidence of IBH was higher in horses imported out of the IBH season compared to import during the IBH season but this difference was not statistically significant. Similarly to earlier publications [6, 8], we found no influence of gender or age at importation on the incidence of IBH. However, our study group only consisted of Icelandic horses exported as adults (4–12 years). The incidence of IBH in Icelandic horses exported at young age (7–10 months) is much lower than if exported as adults and is similar to that of Icelandic horses born in Europe . This might be explained by a higher capability of foals to make a regulatory immune response compared to adults . The age at first exposure to Culicoides spp. appears thus to be an important predisposing factor [1, 27], while, unlike for horses born in Culicoides-rich environments, genetic factors probably play a minor role [6, 10].
The CAST has been evaluated thoroughly for its use with C. nubeculosus and S. vittatum extracts to confirm a clinical diagnosis of IBH . A high specificity (> 95%) of this test with C. nubeculosus extract with a sensitivity of 78% was found, while specificity and sensitivity were lower with S. vittatum extract. Our aim was to investigate whether Icelandic horses that would develop IBH following exportation to Culicoides spp. areas would already be positive in CAST before the first onset of clinical signs and also, whether horses sensitized to S. vittatum in Iceland would be more prone to develop IBH after importation to Culicoides-rich environments. To establish the baseline values, 128 horses that remained in Iceland and 40 horses from the follow up study were tested in the CAST in Iceland. Only one out of a total of 168 horses showed a positive test result with C. nubeculosus, confirming earlier studies [29, 30]. The results after stimulation with S. vittatum are more interesting because S. vittatum are the only haematophagous flies that bite horses in Iceland . The S. vittatum extract was made from S. vittatum captured from the wild in Iceland. However, only four of the 128 horses bled in the Simulium season reacted to the extract and there were no differences between horses coming from high and low Simulium environment. From the 40 horses tested before export, only one was positive upon stimulation with S. vittatum. This horse, tested and exported at the end of summer, was positive in the CAST with both extracts a few months after arriving in Switzerland and developed clinical IBH the following summer. This suggests that the horse was already sensitized to S. vittatum allergens before export, but without clinical signs of IBH. In general, Culicoides spp. allergens seem to be needed as sensitizers whereas after sensitization many of the allergic horses cross-react to homologous proteins from Simulium spp. Immunological cross-reactivity is a well-known phenomenon in allergy . Homologous allergens found in Simulium spp. and Culicoides spp. that share common epitopes have been documented [19, 25, 32].
The percentage of horses showing a positive CAST with C. nubeculosus increased over time and got significantly higher in the endpoint IBH compared to the H group after the second summer following import, reaching a peak after the third summer with 63% of the endpoint IBH and 12% of the endpoint H horses being positive. After the 4th summer the percentage of positive horses decreased to 50% in the endpoint IBH group, probably because most IBH-affected horses were treated, i.e. exposure to the allergens was strongly reduced. The results of the CAST could not be evaluated in all horses at all time points because blood samples were not always available and because of non-responders [4, 21]. A complete data set over four summers was thus only available for 29 and 27 endpoint H and IBH horses, respectively. With these horses we investigated whether horses that developed IBH gave a positive CAST result in the years preceding first clinical signs. Twenty-six percent and 20% of these horses were positive in the CAST with C. nubeculosus 1 and 2 years before clinical IBH, respectively. Nevertheless, these results were not useful to identify IBH predisposed horses because 8–17% of the endpoint H horses were also positive in the test. However, most of the horses of the H endpoint group became negative in the following years, while 60% of the IBH group was positive in the CAST in the year when clinical signs first occurred and this percentage increased to nearly 70% 1 year later (Fig. 4). At all time points there were more horses positive with S. vittatum than with C. nubeculosus and at T − 1 there were more endpoint H than IBH horses positive in CAST with this allergen. With both insect extracts a significant difference between the H and IBH endpoint group was thus only obtained when the horses become clinically affected with IBH. The proportion of healthy horses positive in the CAST with C. nubeculosus was higher than what was found previously in a study where only horses living for many years in Switzerland were included (17% versus < 5%; ). We do not know why a relatively high proportion of the H endpoint horses were positive in the CAST. Interestingly, most of them became CAST negative again later on. This suggests that a majority of horses become sensitized to these insects to some degree but that regulatory mechanisms may then control sensitization [33, 34].
The major findings of this study are that 50% of Icelandic horses imported from Iceland develop IBH following import into Switzerland and that exposure to insect bites such as Culicoides spp. for at least one but usually for two to three summers is required to develop IBH. This indicates that horses in Iceland are not sensitized against Culicoides spp. or Simulium spp., although the latter are native to Iceland, a result that was confirmed by the CAST. Importantly, the present study shows that a positive CAST result when stimulating with C. nubeculosus in horses recently imported from Iceland can only be used to confirm clinical cases of IBH. The CAST should not be used to identify horses predisposed to IBH before occurrence of first clinical signs, because a part of the horses that remain free of this disease can be transiently positive in the test. This suggests that horses can be sensitized to Culicoides spp. allergens to some degree but that regulatory mechanisms may then control further development of the disease.
EM, ST, VS and SB designed the study. EM, VS, SS, SB and WH performed the clinical examinations of the horses and took the blood samples. EM, ST, and SB performed the sLT release assay. EM, SJ and SS carried out the statistical analyses. EM, ST, SJ and SS wrote the manuscript. All authors read and approved the final manuscript.
We thank Bühlmann Laboratories AG, Schönenbuch, Switzerland, for providing the CAST and all the horse owners for participating to this study. We are grateful to Marcus Doherr, Faculty of Veterinary Medicine, Institute for Veterinary Epidemiology and Biostatistics, Freie Universität Berlin, Germany, for his useful advice for the statistical analyses.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
The study was approved by the Animal Experimental Committee of the Canton of Berne, Switzerland (No. BE 121/05).
This work was supported by the Swiss National Science Foundation grant No. 310000-116803, and by the Agricultural Productivity Fund of Iceland.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Schaffartzik A, Hamza E, Janda J, Crameri R, Marti E, Rhyner C. Equine insect bite hypersensitivity: what do we know? Vet Immunol Immunopathol. 2012;147:113–26.View ArticleGoogle Scholar
- Baker KP, Quinn PJ. A report on clinical aspects and histopathology of sweet itch. Equine Vet J. 1978;10:243–8.View ArticleGoogle Scholar
- Fadok VA, Greiner EC. Equine insect hypersensitivity: skin test and biopsy results correlated with clinical data. Equine Vet J. 1990;22:236–40.View ArticleGoogle Scholar
- Baselgia S, Doherr MG, Mellor P, Torsteinsdottir S, Jermann T, Zurbriggen A, et al. Evaluation of an in vitro sulfidoleukotriene release test for diagnosis of insect bite hypersensitivity in horses. Equine Vet J. 2006;38:40–6.View ArticleGoogle Scholar
- Johannsson V. The life cycles of Simulium vittatum ZETT in Icelandic lake-outlets. Verh Int Verein Limnol. 1988;23:2170–8.Google Scholar
- Björnsdóttir S, Sigvaldadóttir J, Broström H, Langvad B, Sigurdsson A. Summer eczema in exported Icelandic horses: influence of environmental and genetic factors. Acta Vet Scand. 2006;48:3.View ArticleGoogle Scholar
- Broström H, Larsson Å, Troedsson M. Allergic dermatitis (sweet itch) of Icelandic horses in Sweden: an epidemiological study. Equine Vet J. 1987;19:229–36.View ArticleGoogle Scholar
- Halldorsdottir S, Larsen HJ. An epidemiological study of summer eczema in Icelandic horses in Norway. Equine Vet J. 1991;23:296–9.View ArticleGoogle Scholar
- van Grevenhof EM, Ducro B, Heuven HC, Bijma P. Identification of environmental factors affecting the prevalence of insect bite hypersensitivity in Shetland ponies and Friesian horses in The Netherlands. Equine Vet J. 2007;39:69–73.View ArticleGoogle Scholar
- Marti E, Gerber V, Wilson AD, Lavoie JP, Horohov D, Crameri R, et al. Report of the 3rd Havemeyer workshop on allergic diseases of the horse, Hólar, Iceland, June 2007. Vet Immunol Immunopathol. 2008;126:351–61.View ArticleGoogle Scholar
- Peeters LM, Janssens S, Brebels M, Buys N. Genetic parameters and estimated breeding values of insect bite hypersensitivity in Belgian Warmblood horses. Vet J. 2015;206:420–2.View ArticleGoogle Scholar
- Citek J, Vostry L, Vostra-Vydrova H, Brzakova M, Prantlova V. Genetic parameters of insect bite hypersensitivity in the old grey Kladruber horse. J Anim Sci. 2017;95:53–8.PubMedGoogle Scholar
- Shrestha M, Eriksson S, Schurink A, Andersson LS, Sundquist M, Frey R, et al. Genome-wide association study of insect bite hypersensitivity in Swedish-born Icelandic horses. J Hered. 2015;106:366–74.View ArticleGoogle Scholar
- Velie BD, Shrestha M, Franҫois L, Schurink A, Tesfayonas YG, Stinckens A, et al. Using an inbred horse breed in a high density genome-wide scan for genetic risk factors of insect bite hypersensitivity (IBH). PLoS ONE. 2016;11(4):e0152966.View ArticleGoogle Scholar
- Hellberg W, Wilson D, Mellor P, Doherr M, Torsteinsdottir S, Zurbriggen A, et al. Equine insect bite hypersensitivity: immunoblot analysis of IgE and IgG subclass responses to Culicoides nubeculosus salivary gland extract. Vet Immunol Immunopathol. 2006;113:99–112.View ArticleGoogle Scholar
- Wilson AD, Harwood LJ, Björnsdottir S, Marti E, Day MJ. Detection of IgG and IgE serum antibodies to Culicoides salivary gland antigens in horses with insect dermal hypersensitivity (sweet itch). Equine Vet J. 2001;33:707–13.View ArticleGoogle Scholar
- Wilson AD, Heesom KJ, Mawby WJ, Mellor PS, Russell CL. Identification of abundant proteins and potential allergens in Culicoides nubeculosus salivary glands. Vet Immunol Immunopathol. 2008;122:94–103.View ArticleGoogle Scholar
- Langner KF, Jarvis DL, Nimtz M, Heselhaus JE, McHolland LE, Leibold W, et al. Identification, expression and characterisation of a major salivary allergen (Cul s 1) of the biting midge Culicoides sonorensis relevant for summer eczema in horses. Int J Parasitol. 2009;39:243–50.View ArticleGoogle Scholar
- Schaffartzik A, Marti E, Torsteinsdottir S, Mellor PS, Crameri R, Rhyner C. Selective cloning, characterization, and production of the Culicoides nubeculosus salivary gland allergen repertoire associated with equine insect bite hypersensitivity. Vet Immunol Immunopathol. 2011;139:200–9.View ArticleGoogle Scholar
- van der Meide NM, Savelkoul HF, Meulenbroeks C, Ducro BJ, Tijhaar E. Evaluation of a diagnostic ELISA for insect bite hypersensitivity in horses using recombinant obsoletus complex allergens. Vet J. 2014;200:31–7.View ArticleGoogle Scholar
- Marti E, Urwyler A, Neuenschwander M, Eicher R, Meier D, de Weck AL, et al. Sulfidoleukotriene generation from peripheral blood leukocytes of horses affected with insect bite dermal hypersensitivity. Vet Immunol Immunopathol. 1999;71:307–20.View ArticleGoogle Scholar
- Langner KF, Darpel KE, Drolet BS, Fischer A, Hampel S, Heselhaus JE, et al. Comparison of cellular and humoral immunoassays for the assessment of summer eczema in horses. Vet Immunol Immunopathol. 2008;122:126–37.View ArticleGoogle Scholar
- Wagner B, Childs BA, Erb HN. A histamine release assay to identify sensitization to Culicoides allergens in horses with skin hypersensitivity. Vet Immunol Immunopathol. 2008;126:302–8.View ArticleGoogle Scholar
- Hellberg W, Mellor PS, Torsteinsdóttir S, Marti E. Insect bite hypersensitivity in the horse: comparison of IgE-binding proteins in salivary gland extracts from Simulium vittatum and Culicoides nubeculosus. Vet Immunol Immunopathol. 2009;132:62–7.View ArticleGoogle Scholar
- Schaffartzik A, Marti E, Crameri R, Rhyner C. Cloning, production and characterization of antigen 5 like proteins from Simulium vittatum and Culicoides nubeculosus, the first cross-reactive allergen associated with equine insect bite hypersensitivity. Vet Immunol Immunopathol. 2010;137:76–83.View ArticleGoogle Scholar
- Lange S, Hamann H, Deegen E, Ohnesorge B, Distl O. Investigation of the prevalence of summer eczema in Icelandic horses in northern Germany. Berl Munch Tierarztl Wochenschr. 2005;118:481–9.PubMedGoogle Scholar
- Sommer-Locher B, Endriss V, Fromm E. Various circumstances regarding initial allergen exposure and their influence on development of insect bite hypersensitivity in horses. J Equine Vet Sci. 2012;32:158–63.View ArticleGoogle Scholar
- Hamza E, Mirkovitch J, Steinbach F, Marti E. Regulatory T cells in early life: comparative study of CD4+ CD25high T cells from foals and adult horses. PLoS ONE. 2015;10:e0120661.View ArticleGoogle Scholar
- Larsen HJ, Bakke SH, Mehl R. Intradermal challenge of Icelandic horses in Norway and Iceland with extracts of Culicoides spp. Acta Vet Scand. 1988;29:311–4.PubMedGoogle Scholar
- Ziegler A, Hamza E, Jonsdottir S, Rhyner C, Wagner B, Schüpbach G, et al. Longitudinal analysis of allergen-specific IgE and IgG subclasses as potential predictors of insect bite hypersensitivity following first exposure to Culicoides in Icelandic horses. Vet Dermatol. 2018;29:51-e22.View ArticleGoogle Scholar
- Aalberse RC. Assessment of allergen cross-reactivity. Clin Mol Allergy. 2007;5:2.View ArticleGoogle Scholar
- Schaffartzik A, Weichel M, Crameri R, Björnsdóttir TS, Prisi C, Rhyner C, et al. Cloning of IgE-binding proteins from Simulium vittatum and their potential significance as allergens for equine insect bite hypersensitivity. Vet Immunol Immunopathol. 2009;132:68–77.View ArticleGoogle Scholar
- Hamza E, Steinbach F, Marti E. CD4+ CD25+ T cells expressing FoxP3 in Icelandic horses affected with insect bite hypersensitivity. Vet Immunol Immunopathol. 2012;148:139–44.View ArticleGoogle Scholar
- Hamza E, Akdis CA, Wagner B, Steinbach F, Marti E. In vitro induction of functional allergen-specific CD4+ CD25high Treg cells in horses affected with insect bite hypersensitivity. Clin Exp Allergy. 2013;43:889–901.View ArticleGoogle Scholar