Production of a monoclonal antibody to canine thymus and activation-regulated chemokine (TARC) and detection of TARC in lesional skin from dogs with atopic dermatitis
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Maeda, S
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Maeda, S
Tsukui, T
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Tsukui, T
Saze, KI
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Saze, KI
Masuda, K
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Masuda, K
Ohno, K
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Ohno, K
Tsujimoto, H
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Tsujimoto, H
Iwabuchi, S
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机构:Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
Iwabuchi, S
机构:
[1] Nippon Zenyaku Kogyo Co Ltd, Cent Res Labs, Fukushima 9630196, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Vet Internal Med, Bunkyo Ku, Tokyo 1138657, Japan
A monoclonal antibody to canine thymus and activation-regulated chemokine (TARC/CCL17) was developed to examine the association of TARC with the immunopathogenesis of canine atopic dermatitis (AD). Recombinant canine TARC was prepared using an E. coli expression system. Results of transwell chemotaxis assay demonstrated that the recombinant canine TARC showed chemotactic activity for canine lymphoid cells expressing CC chemokine receptor 4 (CCR4). Mice were then immunized with the recombinant canine TARC to obtain monoclonal antibodies. Among the monoclonal antibodies thereby obtained, one monoclonal antibody (CTA-1) was found to react with both recombinant and authentic canine TARC in ELISA and flowcytometric assays, respectively. Immunohistochemical analysis using the monoclonal antibody CTA-1 demonstrated that keratinocytes were major TARC producing cells in lesional skin of dogs with AD. (C) 2004 Elsevier B.V. All rights reserved.