Effect of Both Ultraviolet B Irradiation and Histamine Receptor Function on Allergic Responses to an Inhaled Antigen1
Effect of Both Ultraviolet B Irradiation and Histamine Receptor Function on Allergic Responses to an Inhaled Antigen1
复制标题
紫外线 B 照射和组胺受体功能对吸入抗原过敏反应的影响1
作者:
Jacqueline P. McGlade;S. Gorman;J. Lenzo;Jamie W. Tan;Takeshi Watanabe;J. Finlay;W. Thomas;P. Hart
Exposure of skin to UVB radiation (290–320 nm) modulates the immune system, with most studies showing a suppression of Th1-driven immune responses. This study investigated the effects of UVB on Th2-associated immune responses using a murine model of allergic respiratory inflammation. C57BL/6, histamine receptor-1 knockout (H1RKO), and histamine receptor-2 knockout (H2RKO) mice were exposed to a single 4 kJ/m2 dose of UVB (twice a minimal edemal dose) on shaved dorsal skin 3 days before intranasal sensitization with papain, a cysteine protease homologue of the dust mite allergen Der p 1. H1RKO mice demonstrated enhanced papain-specific inflammatory responses in the lung-draining lymph nodes (LDLNs), whereas the responses of H2RKO mice closely mimicked those of C57BL/6 mice. UVB irradiation 3 days before sensitization reduced in vitro papain-specific proliferation of LDLN cells of C57BL/6 and H1RKO mice but not H2RKO mice 24 h after challenge. The regulatory effect of UVB was transferred by adoptive transfer of unfractionated LDLN cells from UVB-irradiated, papain-sensitized C57BL/6 and H1RKO donor mice in naive recipients of the corresponding strain that were subsequently sensitized and challenged with papain. Additionally, UVB exposure suppressed papain-induced IL-5 and IL-10 production in vitro by LDLN cells from H1RKO mice but not from C57BL/6 mice or H2RKO mice. The results of this study demonstrate systemic immunomodulation of responses to intranasally delivered Ag by UVB irradiation and implicate a role for the H2 receptor in UVB-induced suppression of Ag-specific responses in the draining lymph nodes.
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影响因子:
--
作者:
I. Walters;M. Ozawa;I. Cardinale;P. Gilleaudeau;W. Trepicchio;J. Bliss;J. Krueger
通讯作者:
I. Walters;M. Ozawa;I. Cardinale;P. Gilleaudeau;W. Trepicchio;J. Bliss;J. Krueger
影响因子:
4.3
作者:
Khan,MM;Keaney,KM;Melmon,KL;Clayberger,C;Krensky,AM
通讯作者:
Krensky,AM
影响因子:
6.5
作者:
Nghiem, DX;Kazimi, N;Ullrich, SE
通讯作者:
Ullrich, SE
影响因子:
4.6
作者:
Barrios,RobertoJ;Kheradmand,Farrah;Batts,LaKeisha;Corry,DavidB
通讯作者:
Corry,DavidB
DOI:
10.1172/jci111863
发表时间:
1985
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Khan,MM;Sansoni,P;Engleman,EG;Melmon,KL
通讯作者:
Melmon,KL