| Literature DB >> 26876716 |
Clare Murray1, Kim Ahrens2, Matt Devalaraja3, Mike Dymond1, Malbinder Fagura1, Adam Hargreaves1, Alison Holt1, Ian Peers1, Sally Price1, Jaimini Reens1, Rob Riley1, Rosanna Marsella4.
Abstract
Atopic dermatitis (AD) is an inflammatory skin disease characterized by infiltration of skin homing lymphocytes into the dermis. Most of these lymphocytes express the chemokine receptor CCR4, and the frequency of blood CCR4(+) lymphocytes correlates with AD disease severity. Canine AD is a pruritic inflammatory condition that shows many features of the human disease, including CCR4 overexpression. Therefore, we tested a potent selective CCR4 antagonist in an allergen challenge model of canine AD, both clinically and histologically, to investigate whether this chemokine pathway plays a role in the inflammatory response. Using a four-period randomized cross-over study design, 14 beagles were challenged with allergen and clinically monitored. Biopsy samples were taken before and after allergen challenge. A clear reduction of clinical scores was observed with oral prednisolone (P < 0.0001) but not for the CCR4 inhibitor. A subset of the dogs (5/13) showed partial inhibition (30-49%) of the clinical signs with CCR4 inhibitor treatment, and this finding was supported by the results of histopathologic analysis of skin biopsy samples. This partial response is consistent with redundancy in chemokine pathways and highlights the need for therapies blocking multiple pathways. This study shows the utility of this canine model of AD for testing new therapeutic agents.Entities:
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Year: 2015 PMID: 26876716 DOI: 10.1016/j.jid.2015.11.001
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551