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DOI 10.3892/etm.2017.4810

Медицинская библиотека · Experimental and therapeutic medicine · 2017

Evaluation of hyaluronic acid-P40 conjugated cream in a mouse model of dermatitis induced by oxazolone.

Mangano Katia, Vergalito Franca, Mammana Santa, Mariano Andrea, De Pasquale Rocco, Meloscia Antonia, Bartollino Silvia, Guerra Germano, Nicoletti Ferdinando, Di Marco Roberto

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Аннотация

P40 is a particulate fraction or fragment isolated from Corynebacterium granulosum, which exhibits a wide spectrum of pharmacological functions including antitumor, antibacterial, phagocytic, antiviral and cytokine induction effects. In the present study, the immunomodulatory potential of P40-conjugated with hyaluronic acid was assessed in a mouse model of dermatitis induced by oxazolone. Oxazolone-induced allergic contact dermatitis is a T cell-mediated Th2-like hypersensitivity reaction, which mimics the corresponding reaction in humans. Female cluster of differentiation-1 mice were sensitized on days 0 and 1 by the application of 2% oxazolone onto a shaved back. The disease was induced by re-challenge on day 7 using 15% oxazolone in the inner and outer of the left ears of the mice. Mice were topically treated with hyaluronic acid-P40 conjugate cream or with placebo to the inner and outer surface of the left ear for 7 consecutive days starting from 1 h after the sensitization. A significant reduction in ear thickness and weight and in edema and leukocyte recruitment were observed in the mice treated with hyaluronic-P40 conjugate cream compared with mice treated with the cream base alone (P<0.05). Thus, P40-conjugated with hyaluronic acid may constitute an innovative dermatitis treatment.

Для цитирования: Mangano Katia, Vergalito Franca, Mammana Santa, Mariano Andrea, De Pasquale Rocco, Meloscia Antonia, Bartollino Silvia, Guerra Germano, Nicoletti Ferdinando, Di Marco Roberto. Evaluation of hyaluronic acid-P40 conjugated cream in a mouse model of dermatitis induced by oxazolone.. Experimental and therapeutic medicine. 2017. DOI: 10.3892/etm.2017.4810.
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