共 70 条
CD52 is a novel costimulatory molecule for induction of CD4+ regulatory T cells
被引:124
作者:

Watanabe, Tomoko
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Masuyama, Jun-ichi
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Sohma, Yoshiaki
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Inazawa, Hiroko
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Horie, Kaori
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Kojima, Kumiko
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Uemura, Yasunori
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Aoki, Yumi
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Kaga, Shuji
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Minota, Seiji
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Tanaka, Toshiyuki
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Yamaguchi, Yasunori
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Kobayashi, Tetsuto
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan

Serizawa, Isao
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机构: Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan
机构:
[1] Kirin Brewery Co Ltd, Div Pharmaceut, Cellular Immunotherapy Pharmaceut Res Labs, Takasaki, Gumma 3701295, Japan
[2] Jichi Med Sch, Dept Med, Div Rheumatol & Clin Immunol, Minami Kawachi, Tochigi 3290498, Japan
[3] Showa Univ, Dept Med 1, Tokyo 1428555, Japan
[4] Osaka Univ, Grad Sch Med, Lab Mol & Cellular Recognit, Suita, Osaka 5650871, Japan
关键词:
human;
T cells;
regulatory T cells;
suppressor T cells;
D O I:
10.1016/j.clim.2006.05.006
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
We previously reported that 4C8 monoclonal antibody (mAb) provides a costimulatory signal to human CD4(+) T cells and consequently induces regulatory T (Treg) cells, which are hypo-responsive and suppress the polyclonal response of bystander CD4(+) cells in a contact-dependent manner. In this study, we identified the antigen of 4C8 mAb as CD52. Costimulation with Campath-1H, a humanized anti-CD52 mAb, also induced Treg cells. Anti-CD52-induced Treg cells suppressed the proliferation of both CD4(+) and CD8(+) T cells provided with polyclonal or allogeneic stimulation. When Treg cells were induced from Staphylococcal enterotoxin B (SEB) treated cells, they suppressed the response to SEB more efficiently than that to another superantigen, SEA. Furthermore, anti-CD52-induced Treg cells could be expanded by culture with IL-2 followed by CD52-costimulation, and co-injection of expanded Treg cells suppressed lethal xenogeneic graft versus host disease (GvHD) reactions in SCID mice caused by human peripheral blood mononuclear cells (PBMCs). (c) 2006 Elsevier Inc. All rights reserved.
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页码:247 / 259
页数:13
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UNIV GOTTINGEN,DEPT HEMATOL ONCOL,D-3400 GOTTINGEN,GERMANY UNIV GOTTINGEN,DEPT HEMATOL ONCOL,D-3400 GOTTINGEN,GERMANY

Kapp, A
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UNIV GOTTINGEN,DEPT HEMATOL ONCOL,D-3400 GOTTINGEN,GERMANY UNIV GOTTINGEN,DEPT HEMATOL ONCOL,D-3400 GOTTINGEN,GERMANY