UVB Exposure Prevents Atherosclerosis by Regulating Immunoinflammatory Responses

Naoto Sasaki1, Tomoya Yamashita2, Kazuyuki Kasahara2

  • 1From the Division of Cardiovascular Medicine, Department of Internal Medicine (N.S., T. Yamashita., K.K., T.E., K.Y., T. Matsumoto, K.N., T.K., M.T., T. Mizoguchi, T.H., Y.S., K.-i.H.) and Division of Dermatology, Department of Internal Related (A.F., M.H., K.T., K.W., C.N.), Kobe University Graduate School of Medicine, Japan; Department of Medical Pharmaceutics, Kobe Pharmaceutical University, Japan (N.S.); Department of Single Molecule Imaging (T. Yamaguchi) and Department of Experimental Immunology (S.S.), World Premier International Immunology Frontier Research Center, Osaka University, Japan; Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Japan (M.T.); and Centre d'Immunologie de Marseille-Luminy and the Centre d'Immunophénomique, UM2 Aix-Marseille Université, Marseille, France (B.M.). n-sasaki@kobepharma-u.ac.jp tomoya@med.kobe-u.ac.jp.

Summary

Ultraviolet B (UVB) irradiation prevents atherosclerosis development in mice by boosting regulatory T cells. This suggests the skin immune system could be a new target for treating cardiovascular disease.

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