Treatment with Anti-Interleukin 23 Antibody Ameliorates Disease in Lupus-Prone Mice

被引:35
作者
Kyttaris, Vasileios C. [1 ,2 ]
Kampagianni, Ourania [1 ]
Tsokos, George C. [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Rheumatol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1155/2013/861028
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Interleukin 23 receptor expressing IL-17 producing T cells have been shown to be important in the development of murine lupus. The usefulness of IL-23 inhibition in ameliorating lupus nephritis is unknown. We hypothesized that inhibition of IL-23 will ameliorate nephritis in lupus-prone mice. To this end, we treated MRL/lpr lupus-prone mice for 6 weeks with a rat anti-IL-23p19 antibody, which resulted in delaying the onset of nephritis without affecting the production of anti-dsDNA antibodies. The effect of the treatment was hampered by the production of murine anti-rat IgG antibodies. The amelioration of murine lupus by IL-23 inhibition strengthens the rationale for targeting IL-23 in patients with systemic lupus erythematosus.
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页数:5
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