Immunomodulatory activity of a methionine aminopeptidase-2 inhibitor on B cell differentiation

被引:12
作者
Priest, R. C. [1 ]
Spaull, J. [2 ]
Buckton, J.
Grimley, R. L. [2 ]
Sims, M.
Binks, M.
Malhotra, R.
机构
[1] GlaxoSmithKline Inc, CEDD 2, Discovery Biomed, R&D, Stevenage SG1 NY, Herts, England
[2] GlaxoSmithKline Inc, R&D, MDR, Stevenage SG1 NY, Herts, England
关键词
B cell differentiation; germinal centre; methionine aminopeptidase-2; FACTOR 2-ASSOCIATED GLYCOPROTEIN; RHEUMATOID-ARTHRITIS; SYNTHETIC ANALOGS; ANGIOGENESIS; FUMAGILLIN; OVALICIN; TYPE-2; PROLIFERATION; AGM-1470; PPI-2458;
D O I
10.1111/j.1365-2249.2008.03843.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Methionine aminopeptidase-2 (MetAP-2) inhibitors have potent anti-angiogenesis activity and are being developed for the treatment of solid tumours. The recently observed specific expression of MetAP-2 in germinal centre B cells suggests that it has a role in regulating B cell function. We have demonstrated a potent MetAP-2-dependent inhibitory effect on the antibody secretion from B cell receptor and CD40 co-stimulated primary human B cells in the presence of interleukin-21. The effect of MetAP-2 inhibition on antibody secretion was due to a block in differentiation of B cells into plasma cells. Immunohistochemical analysis of germinal centres from human, mouse and marmoset spleen showed a similar expression pattern of MetAP-2 in the marmoset and man, whereas mouse spleen showed no detectable expression. In a marmoset, T dependent immunization model, the MetAP-2 inhibitor suppressed an antigen-specific antibody response. Furthermore, histological analysis showed loss of B cells in the spleen and disrupted germinal centre formation. These results provide experimental evidence to support a novel role for MetAP-2 in immunomodulation. These effects of MetAP-2 are mediated by disruption of the germinal centre reaction and a block in the differentiation of B cells into plasma cells.
引用
收藏
页码:514 / 522
页数:9
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