Cyclophosphamide decreases the number, percentage and the function of CD25+ CD4+ regulatory T cells, which suppress induction of contact hypersensitivity

被引:90
作者
Ikezawa, Y
Nakazawa, M
Tamura, C
Takahashi, K
Minami, M
Ikezawa, Z
机构
[1] Yokohama City Univ, Grad Sch Med, Dept Environm Immunodermatol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[2] Yokohama City Univ, Grad Sch Med, Dept Immunol, Yokohama, Kanagawa 2360004, Japan
关键词
cyclophosphamide (Cy); contact hypersensitivity reaction; CD25(+) CD24(+) regulatory T cell;
D O I
10.1016/j.jdermsci.2005.02.002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: It is well known that cyclophosphamide (Cy) treatment before sensitization paradoxically enhances rather than suppresses contact hypersensitivity (CH) reactions. In fact, Cy-treated mice developed a significant (p < 0.05) increase of the CH reactions to 2,4,6-trinitro-1-chrolobenzene (TNCB) in comparison with untreated mice. Objective: In order to examine whether the target cells of Cy in the immunoaugmentative effect are CD25(+) CD4(+) regulatory T cells or not, we investigated effect of Cy treatment on CD25(+) CD4(+) T cells. Method: We examined Cy-treated CD25(+) CD4(+) T cells by flow cytometer and by inhibition assay on proliferation of CD25(+) CD4(+) T cells. Results: Cy treatment remarkably reduced the number and percentage of CD25(+) CD4(+) T cells in the spleen and lymph nodes 3 and 5 days later. Moreover, CD25(+) CD4(+) T cells taken from the Cy-treated mice 3 days later showed the lower suppressive activity on proliferation of CD25(+) CD4(+) T cells, as compared to that from the untreated mice. Furthermore, transfer of CD25(+) CD4(+) T cells from untreated mice resulted in a significant decrease (p < 0.05) of the CH reactions enhanced by Cy treatment. Conclusion: These results indicate that enhancement of the CH reactions to TNCB by Cy treatment is attributed to the decrease in the number, percentage and the function of CD25(+) CD4(+) regulatory T cells. (c) 2005 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 33 条
[1]   Involvement of dectin-2 in ultraviolet radiation-induced tolerance [J].
Aragane, Y ;
Maeda, A ;
Schwarz, A ;
Tezuka, T ;
Ariizumi, K ;
Schwarz, T .
JOURNAL OF IMMUNOLOGY, 2003, 171 (07) :3801-3807
[2]  
ASHERSON GL, 1968, IMMUNOLOGY, V15, P405
[3]   THE EFFECT OF CYCLOPHOSPHAMIDE ON IMMUNOLOGICAL MEMORY [J].
DROSSLER, K ;
PARKER, D ;
TURK, JL .
IMMUNOPHARMACOLOGY, 1983, 6 (02) :123-132
[4]   Innate CD4+CD25+ regulatory T cells are required for oral tolerance and inhibition of CD8+ T cells mediating skin inflammation [J].
Dubois, B ;
Chapat, L ;
Goubier, A ;
Papiernik, M ;
Nicolas, JF ;
Kaiserlian, D .
BLOOD, 2003, 102 (09) :3295-3301
[5]  
Furtado GD, 2001, IMMUNOL REV, V182, P122
[6]   CD4+CD25+ regulatory T cells suppress tumor immunity but are sensitive to cyclophosphamide which allows immunotherapy of established tumors to be curative [J].
Ghiringhelli, F ;
Larmonier, N ;
Schmitt, E ;
Parcellier, A ;
Cathelin, D ;
Garrido, C ;
Chauffert, B ;
Solary, E ;
Bonnotte, B ;
Martin, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (02) :336-344
[7]   Functional alteration of peripheral CD25+CD4+ immunoregulatory T cells in a transgenic rat model of autoimmune diseases [J].
Higuchi, M ;
Ishizu, A ;
Ikeda, H ;
Hayase, H ;
Fugo, K ;
Tsujia, M ;
Abe, A ;
Sugaya, T ;
Suzuki, A ;
Takahashi, T ;
Koike, T ;
Yoshiki, T .
JOURNAL OF AUTOIMMUNITY, 2003, 20 (01) :43-49
[8]   Characterization of dermatitis arising spontaneously in DS-Nh mice maintained under conventional conditions: another possible model for atopic dermatitis [J].
Hikita, I ;
Yoshioka, T ;
Mizoguchi, T ;
Tsukahara, K ;
Tsuru, K ;
Nagai, H ;
Hirasawa, T ;
Tsuruta, Y ;
Suzuki, R ;
Ichihashi, M ;
Horikawa, T .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2002, 30 (02) :142-153
[9]  
IKEZAWA Z, 1980, JPN J EXP MED, V50, P225
[10]  
IKEZAWA Z, 1987, IMMUNOLOGY, V60, P375