The induction of immunity to a protein antigen using an adjuvant is significantly compromised by ultraviolet A radiation

被引:16
作者
Byrne, Scott N. [1 ]
Spinks, Nik [1 ]
Halliday, Gary M. [1 ]
机构
[1] Univ Sydney, Dept Med, Dermatol Res Labs,Royal Prince Alfred Hosp, Melanoma & Skin Canc Res Inst,Sydney Canc Ctr, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
sunlight; ultraviolet; immunosuppression; skin cancer; immunomodulation;
D O I
10.1016/j.jphotobiol.2006.02.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ultraviolet (UV) radiation from sunlight causes skin cancer and inhibits priming of the immune system during vaccination. However the dose related effects of the different components of sunlight (UVA and UVB) are complex and require further investigation. Using ovalbumin as a model protein vaccine with saponin as adjuvant we show that both UVA and UVB can suppress the DTH response to a poorly immunogenic protein. Increasing doses of UVB induced increased levels of immunosuppression and tolerance. UVA however, caused a bi-phasic dose response with intermediate but not low or high doses causing primary immunosuppression. No dose of UVA caused significant tolerance. Similar results were observed in both C57BL/6 and Balb/c mice. Our data confirms the complex immunomodulatory dose effects of UVA and UVB for a protein antigen, and shows that both UVB and UVA can suppress immunity induced by a protein with adjuvant. This highlights the importance of considering sun exposure patterns in the future success of both preventing skin cancer development and enhancing vaccination regimes. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 134
页数:7
相关论文
共 45 条
[1]   The basal layer in human squamous tumors harbors more UVA than UVB fingerprint mutations: A role for UVA in human skin carcinogenesis [J].
Agar, NS ;
Halliday, GM ;
Barnetson, RS ;
Ananthaswamy, HN ;
Wheeler, M ;
Jones, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4954-4959
[2]   HOW MUCH MELANOMA IS CAUSED BY SUN EXPOSURE [J].
ARMSTRONG, BK ;
KRICKER, A .
MELANOMA RESEARCH, 1993, 3 (06) :395-401
[3]   High ultraviolet A protection affords greater immune protection confirming that ultraviolet A contributes to photoimmunosuppression in humans [J].
Baron, ED ;
Fourtanier, A ;
Compan, D ;
Medaisko, C ;
Cooper, KD ;
Stevens, SR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :869-875
[4]  
Brown DB, 2000, PHOTOCHEM PHOTOBIOL, V72, P340, DOI 10.1562/0031-8655(2000)072<0340:CFSAAI>2.0.CO
[5]  
2
[6]   Ultraviolet B but not A radiation activates suppressor B cells in draining lymph nodes [J].
Byrne, SN ;
Ahmed, J ;
Halliday, GM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2005, 81 (06) :1366-1370
[7]   B cells activated in lymph nodes in response to ultraviolet irradiation or by interleukin-10 inhibit dendritic cell induction of immunity [J].
Byrne, SN ;
Halliday, GM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2005, 124 (03) :570-578
[8]   Ultraviolet A irradiation of C57BL/6 mice suppresses systemic contact hypersensitivity or enhances secondary immunity depending on dose [J].
Byrne, SN ;
Spinks, N ;
Halliday, GM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (04) :858-864
[9]   Interleukin-1β but not tumor necrosis factor is involved in West Nile Virus-induced Langerhans cell migration from the skin in C57BL/6 mice [J].
Byrne, SN ;
Halliday, GM ;
Johnston, LJ ;
King, NJC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (03) :702-709
[10]   ULTRAVIOLET-RADIATION DECREASES THE GRANULOMATOUS RESPONSE TO LEPROMIN IN HUMANS [J].
CESTARI, TF ;
KRIPKE, ML ;
BAPTISTA, PL ;
BAKOS, L ;
BUCANA, CD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (01) :8-13