Immunomodulation of experimental APS: Lessons from murine models

被引:13
|
作者
Krause, I
Blank, M
Shoenfeld, Y
机构
[1] CHAIM SHEBA MED CTR,AUTOIMMUNE DIS RES UNIT,DEPT MED B,IL-52621 TEL HASHOMER,ISRAEL
[2] TEL AVIV UNIV,SACKLER FAC MED,IL-69978 TEL AVIV,ISRAEL
关键词
antiphospholipid syndrome; anticardiolipin antibodies; systemic lupus erythematosus; autoimmunity; idiotypes; interleukin-3;
D O I
10.1177/096120339600500526
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During the last few years several murine models for APS have been described. These include spontaneous occurring disease, or APS induced by immunization with pathogenic autoantibodies. Employing those models, several treatment modalities, in different stages of the disease, were studied. Treatments which showed promising potential for application in patients with APS include immunomodulation with specific anti-idiotypic or anti-CD4 antibodies, treatment with IL-3, high-dose intravenous immunoglobulins, ciprofloxacin or bromocriptine, as well as antithrombotic and anticoagulant treatments using aspirin and/or low-molecular-weight heparin. Bone-marrow transplantation was also found to improve clinical and serological manfestations of the disease. These studies might promote the handling of controlled clinical trials assessing their efficacy in APS patients.
引用
收藏
页码:458 / 462
页数:5
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