Long-term effects of IFN-γ, IL-10, and TGF-β-modulated dendritic cells on immune response in Lewis rats

被引:13
|
作者
Duan, RS
Link, H
Xiao, BG
机构
[1] Karolinska Inst, Neurotec, Div Neuroimmunol, SE-14183 Stockholm, Sweden
[2] Fudan Univ, Inst Neurol, Shanghai, Peoples R China
[3] Qianfoshan Hosp, Div Neurol, Shandong, Peoples R China
关键词
autoimmune disease; cytokine; dendritic cell; proliferation;
D O I
10.1007/s10875-005-0357-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Increasing data have shown that IFN-gamma, IL-10, and TGF-beta-modulated dendritic cells ( DC) provide a promising strategy in treatment of experimental allergic encephalomyelitis and experimental autoimmune myasthenia gravis through different manner. To explore the immune response status after long-term application of these cytokine-modulated-DC, Lewis rats were injected subcutaneously into naive DC and IFN-gamma, IL-10, and TGF-beta-modulated DC (i.e., IFN-gamma-DC, IL-10-DC, and TGF-beta-DC) at does of 1 x 10(6) cells/rat every month for continuous 18 months, respectively. No rats suffered from decreased vigor and activity as well as cachectic condition during 18-month observation, and no rats had body-weight loss after 18-month treatment. Exploratory laparectomy did not find any tumor in all rats. IL-10-DC and TGF-beta-DC resulted in lower nonspecific ( Con A-induced) and antigen specific (ovalbumin-stimulated) spleen mononuclear cells proliferation, accompanied by lower levels of IFN-gamma, IL-10, and TNF-alpha. On the contrary, IFN-gamma-DC did not suppress cell proliferation and IFN-alpha and IL-10 production except only slightly decreased TNF-alpha levels. These results suggest that IFN-gamma-DC seems to be a more ideal candidate in the treatment of autoimmune diseases without suppressing immune response.
引用
收藏
页码:50 / 56
页数:7
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