Impaired T cell function in RANTES-deficient mice

被引:103
作者
Makino, Y
Cook, DN
Smithies, O
Hwang, OY
Neilson, EG
Turka, LA
Sato, H
Wells, AD
Danoff, TM
机构
[1] Chiba Univ, Grad Sch Med, Dept Mol Immunol, Chuo Ku, Chiba 2608670, Japan
[2] Chiba Univ, Grad Sch Med, Dept Mol Diag, Chiba 2608670, Japan
[3] Univ Penn, Sch Med, Penn Ctr Mol Studies Kidney Dis, Renal Electrolyte & Hypertens Div, Philadelphia, PA 19104 USA
[4] Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA
[5] Univ N Carolina, Dept Pathol, Chapel Hill, NC 27599 USA
关键词
chemokines; knockout; delayed-type hypersensitivity; cellular proliferation; Th1/Th2;
D O I
10.1006/clim.2001.5178
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The chemokine RANTES is a chemoattractant for monocytes and T cells and is postulated to participate in many aspects of the immune response. To evaluate the biological roles of RANTES in vivo, we generated RANTES-deficient (-/-) mice and characterized their T cell function. In cutaneous delayed-type hypersensitivity assays, a 50% reduction in ear and footpad swelling was seen in -/- mice compared to +/+ mice. In vitro, polyclonal and antigen-specific T cell proliferation was decreased. Quantitative analysis using the fluorescent dye carboxy-fluorescein succinimidyl ester revealed that this proliferative defect was due both to fewer antigen-reactive T cells and to a reduction in the capacity of these cells to proliferate. In addition, IFN-gamma and IL-2 production by the -/- T cells was dramatically decreased. Together, these data suggest that RANTES is required for normal T cell functions as well as for recruiting monocytes and T cells to sites of inflammation. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:302 / 309
页数:8
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