Neutralization of vascular endothelial growth factor prevents collagen-induced arthritis and ameliorates established disease in mice

被引:109
作者
Sone, H
Kawakami, Y
Sakauchi, M
Nakamura, Y
Takahashi, A
Shimano, H
Okuda, Y
Segawa, T
Suzuki, H
Yamada, N
机构
[1] Univ Tsukuba, Inst Clin Med, Dept Internal Med, Tsukuba, Ibaraki 305, Japan
[2] Univ Tsukuba, Dept Clin Pathol, Tsukuba, Ibaraki 305, Japan
[3] Mito Red Cross Hosp, Dept Rheumatol, Mito, Ibaraki 310, Japan
[4] Wakayama Med Coll, Dept Pathol, Wakayama 640, Japan
[5] Toagosei Co Ltd, Tsukuba Res Lab, Biosci Res Dept, Tsukuba, Ibaraki 305, Japan
关键词
vascular endothelial growth factor (VEGF); vascular permeability factor (VPF); rheumatoid arthritis (RA); collagen-induced arthritis (CIA); angiogenesis;
D O I
10.1006/bbrc.2001.4395
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vascular endothelial growth factor (VEGF) is implicated in the pathogenesis of inflammatory joint diseases, including rheumatoid arthritis (RA), To determine the importance of this cytokine in vivo, the effect of administering VEGF-neutralizing antibodies to mice with collagen-induced arthritis (CIA), which has many immunological and pathological similarities to human RA, has been investigated. Either saline, normal rabbit immunoglobulin or anti-human VEGF121 rabbit polyclonal antibody was administered to mice subcutaneously either before the onset of arthritis or after the establishment of clinical disease. Anti-VEGF antibody administered prior to disease onset significantly delayed the development of arthritis and decreased clinical score and paw thickness as well as histological severity. On the other hand, the frequency of occurrence of disease compared to either the control group administered saline or normal rabbit immunoglobulin was not altered. Anti-VEGF antibody also significantly ameliorated clinical and histological parameters even when administered after disease onset. These results indicate a possible therapeutical potential for anti-VEGF treatment in human arthritis. (C) 2001 Academic Press.
引用
收藏
页码:562 / 568
页数:7
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