T cell costimulation by derivatives of benzoic acid

被引:14
|
作者
Kinchington, D
Ng, T
Mathews, N
Tisdale, M
Devine, D
Ayuko, WO
机构
[1] ST BARTHOLOMEWS & ROYAL LONDON SCH MED & DENT,DEPT IMMUNOL,LONDON EC1A 7BE,ENGLAND
[2] ASTON UNIV,INST PHARMACEUT SCI,BIRMINGHAM B4 7ET,W MIDLANDS,ENGLAND
来源
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY | 1997年 / 8卷 / 02期
关键词
costimulation; HIV; immune dysregulation; immunodeficiency; immunomodulator; signal transduction;
D O I
10.1177/095632029700800206
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
A number of analogues of benzoic acid were evaluated in a T cell costimulation assay. One compound, the sodium salt of 2-chloro-5-nitrobenzoic acid (CNBA-Na) was chosen for further study and was found to be a potent costimulator of anti-CD3-induced proliferation of both H9 lymphoblastoid cells (P<0.001) and human peripheral blood mononuclear cells (P=0.001) in a dose-dependent manner. The costimulatory effect of CNBA-Na on CD3-triggered DNA synthesis did not enhance human immunodeficiency virus replication in infected cells. Studies with blocking monoclonal antibodies against B7-1 or B7-2 indicated that the immunopotentiatory effect of CNBA-Na required a macromolecular interaction between CD28 (a costimulatory receptor on T cells) and its counter receptor B7 expressed on antigen-presenting cells. The discovery that this low molecular weight compound causes T cell proliferation highlights a potentially novel therapeutic approach to immunodeficiency diseases.
引用
收藏
页码:121 / 130
页数:10
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