Skip Navigation



Carcinogenesis Advance Access published online on November 20, 2008

Carcinogenesis, doi:10.1093/carcin/bgn248
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
30/1/101    most recent
bgn248v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Yiasemides, E.
Right arrow Articles by Damian, D. L
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yiasemides, E.
Right arrow Articles by Damian, D. L
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Oral nicotinamide protects against ultraviolet radiation-induced immunosuppression in humans

Eleni Yiasemides, Geetha Sivapirabu, Gary M Halliday, Joohong Park and Diona L Damian

Dermatology, Sydney Cancer Centre, Bosch Institute, University of Sydney at Royal Prince Alfred Hospital, Camperdown New South Wales, Australia

Correspondence: A/Professor Diona Damian, Department of Dermatology, Gloucester House Level 3, Royal Prince Alfred Hospital, Missenden Rd, Camperdown NSW 2050 Australia, Phone: +61 2 9515 8295, Fax: +61 2 9565 1048, email: diona.damian{at}email.cs.nsw.gov.au

Cutaneous immunity, which is a key defence against the development of skin cancers, is suppressed by even small doses of ultraviolet (UV) radiation. Preventing this UV-induced immunosuppression may therefore reduce the incidence of skin cancer. Nicotinamide (vitamin B3) has immune-protective and cancer-preventive effects against UV radiation in mice, and we have previously shown that topical nicotinamide is immune-protective in humans. Using the Mantoux model of skin immunity in healthy volunteers, we compared oral nicotinamide to placebo (both administered for one week) in a randomised, double-blinded cross-over design against the effects of solar-simulated (ss) UV radiation on delayed type hypersensitivity to tuberculin purified protein derivative. Discrete areas of the back were irradiated with low doses of ssUV daily for 3 consecutive days. Immunosuppression, calculated as the difference in Mantoux-induced erythema of irradiated sites compared to unirradiated control sites, was determined in volunteers taking oral nicotinamide and placebo. Significant immunosuppression occurred in a UV-dose dependent manner in the presence of placebo. Oral nicotinamide, at doses of either 1500mg or 500mg daily, was well-tolerated and significantly reduced UV-immunosuppression with no immune effects in unirradiated skin. Oral nicotinamide is safe and inexpensive and looks promising as a chemopreventive supplement for reducing the immunosuppressive effects of sunlight.

Key Words: Niacin • Vitamin B3 • Photoprotection • Skin cancer • Delayed type hypersensitivity

Received August 25, 2008; revised October 7, 2008; accepted October 27, 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.