TY - CHAP M1 - Book, Section TI - Chapter 90. Fundamentals of Cutaneous Photobiology and Photoimmunology A1 - Kochevar, Irene E. A1 - Taylor, Charles R. A1 - Krutmann, Jean A2 - Goldsmith, Lowell A. A2 - Katz, Stephen I. A2 - Gilchrest, Barbara A. A2 - Paller, Amy S. A2 - Leffell, David J. A2 - Wolff, Klaus PY - 2012 T2 - Fitzpatrick's Dermatology in General Medicine, 8e AB - |PrintFundamentals of Cutaneous Photobiology and Photoimmunology at a GlanceWhen radiation enters the skin, it is scattered or absorbed. Only light absorbed by molecules (chromophores) in the skin can cause a photobiologic response.Electromagnetic radiation can be conceptualized either as a wave or as packets of energy called photons.An action spectrum indicates which wavelengths produce a photobiologic response most effectively and is plotted as the reciprocal of the minimum effective fluence versus wavelength.The most erythemogenic wavelengths present in sunlight are in the ultraviolet B (UVB) range. Ultraviolet A (UVA) is roughly 1000-fold less effective than UVB.Prostaglandins and nitric oxide appear to be the major mediators for UVB erythema.When certain drugs and dyes absorb UV/visible light, inflammation ensues. This is called photosensitization.Photosensitivity responses are usually mediated by reactive oxygen species.Blocked by sunscreen use, cutaneous vitamin D production is mediated by wavelengths from 295–300 nm. Optimal vitamin D blood levels are essential for good bone health and increasingly associated with a myriad of other potential health benefits.Ultraviolet radiation is immunosuppressive. Local and systemic immunosuppressions are recognized.Pyrimidine dimers, reactive oxygen species and urocanic acid initiate UV-induced immunosuppression.Interleukin-10 (IL-10), tumor necrosis factor (TNF)-α, platelet-activating factor, platelet-activating factor-like lipids and other molecules mediate photoimmunosuppression.The major cellular players in UV immunosuppression are Langerhans cells, keratinocytes, macrophages, and T cells.UV radiation impairs T helper 1-mediated cellular immune response. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/04/24 UR - accessmedicine.mhmedical.com/content.aspx?aid=56050969 ER -