2015
DOI: 10.1292/jvms.14-0338
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Increased proportions of CCR4<sup>+</sup> cells among peripheral blood CD4<sup>+</sup> cells and serum levels of allergen-specific IgE antibody in canine chronic rhinitis and bronchitis

Abstract: Canine chronic rhinitis (CR) and bronchitis (CB) are suspected to be allergic diseases. The present study tested whether dogs diagnosed with CR or CB present an atopic predisposition based on the ratio of CC chemokine receptor 4 (CCR4)-positive cells among peripheral blood CD4-positive cells (CCR4/CD4) and the serum levels of allergen-specific IgE antibodies. We found that most dogs with CR and CB have a possibility of atopic predisposition, and macrolide therapy constitutes an alternative to corticosteroid th… Show more

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Cited by 4 publications
(2 citation statements)
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“…In veterinary medicine, research on antigen-specific IgE has mainly been focused on food allergy [ 71 ], fleabite hypersensitivity [ 72 , 73 ], allergic respiratory diseases [ 74 , 75 , 76 ], and atopic dermatitis [ 53 , 77 , 78 ]. Some private veterinary laboratories propose such allergen-specific IgE testing for clinical application.…”
Section: Humoral In Vitro Testsmentioning
confidence: 99%
“…In veterinary medicine, research on antigen-specific IgE has mainly been focused on food allergy [ 71 ], fleabite hypersensitivity [ 72 , 73 ], allergic respiratory diseases [ 74 , 75 , 76 ], and atopic dermatitis [ 53 , 77 , 78 ]. Some private veterinary laboratories propose such allergen-specific IgE testing for clinical application.…”
Section: Humoral In Vitro Testsmentioning
confidence: 99%
“…White blood cells were isolated from peripheral blood using lysing buffer (BD Biosciences; Franklin Lakes, NJ, USA), followed by an incubation with fluorescein isothiocyanate (FITC)‐conjugated mouse anti‐canine CD3 (clone CA17.2A12, Bio‐Rad Laboratories; Hercules, CA, USA), allophycocyanin (APC)‐conjugated rat anti‐canine CD8 (clone YCATE55.9, Bio‐Rad Laboratories) and phycoerythrin (PE)‐conjugated mouse anti‐human CCR4 (clone 1G1, BD Biosciences) monoclonal antibodies in washing buffer at 4°C for 30 min. Antibodies with appropriate isotypes (FITC‐conjugated mouse IgG1, clone MOPC‐21, Bio Legend; APC‐conjugated rat IgG1, clone 43414, R&D Systems; Minneapolis, MN, USA; PE‐conjugated mouse IgG1, clone MOPC‐21, Bio Legend) were used for each sample.…”
Section: Methodsmentioning
confidence: 99%