2003
DOI: 10.1016/s0165-2427(03)00052-7
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Comparison of intradermal and serum testing for allergen-specific IgE using a FcεRIα-based assay in atopic dogs in the UK

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Cited by 57 publications
(60 citation statements)
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“…Unlike human sensitisations, dogs are more sensitised to D. farinae than to D. pteronyssinus as reported in all European studies (Carlotti and Costargent, 1992;Sture et al, 1995, Saridomichelakis et al, 1999Bensignor and Carlotti, 2002;Foster et al, 2003;Tarpataki et al, 2006), in conformity with our results. The ratio between sensitisations to D. farinae and D. pteronyssinus varies greatly among studies, ranging from 1.06 to 5.37, mainly when sensitisations to D. pteronyssinus are low.…”
Section: Discussionsupporting
confidence: 93%
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“…Unlike human sensitisations, dogs are more sensitised to D. farinae than to D. pteronyssinus as reported in all European studies (Carlotti and Costargent, 1992;Sture et al, 1995, Saridomichelakis et al, 1999Bensignor and Carlotti, 2002;Foster et al, 2003;Tarpataki et al, 2006), in conformity with our results. The ratio between sensitisations to D. farinae and D. pteronyssinus varies greatly among studies, ranging from 1.06 to 5.37, mainly when sensitisations to D. pteronyssinus are low.…”
Section: Discussionsupporting
confidence: 93%
“…Our results show a significant correlation between D. farinae and D. pteronyssinus, similar to the OD correlation reported by Foster et al (2003) using the same test (ALLERCEPT). Nevertheless, the correlation between these two mites was found to be weaker than that reported in studies of humans (Vidal et al, 1997).…”
Section: Discussionsupporting
confidence: 91%
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“…Multiple in vitro assays for detection of allergen-specific IgE are available in the veterinary arena [9,12,16,17,20,23,26], yet there is a paucity of useful data describing the assays and comparing the available tests. The best characterized assays for detection of allergen-specific IgE in dogs are a monoclonal antibody cocktail-based ELISA for dog specific IgE [17] and a human high affinity IgE receptor based assay for dog IgE [6,27]. When directly compared, the concordance of results for these 2 assays was demonstrated to be approximately 92% which is similar to the intra-ELISA/inter-laboratory concordance of results [17].…”
mentioning
confidence: 76%
“…To examine the FcRI expression on cultured cells, the cells were incubated with pooled serum derived from dogs that had been experimentally hypersensitized with Japanese cedar pollen as reported previously [43]. The titer of IgE specific to Japanese cedar pollen antigen in the pooled serum was shown to be more than 2,500 laboratory units by FcRI-based ELISA (Allercept ® Definitive Allergen Panels, Heska, Ft Collins, CO, U.S.A.) [9]. Cells were incubated with 10% of the IgE-rich dog serum and 0.25 g/ml ethidium monoazide (EMA; Molecular Probes, Eugene, OR, U.S.A.) in a wash buffer (PBS containing 2% FBS) for 10 min.…”
Section: Methodsmentioning
confidence: 99%