Martin Roland
Institute for Neuroimmunology and Clinical Multiple Sclerosis Research, Center for Molecular Neurobiology Hamburg, University Medical Center Eppendorf, Hamburg, Germany.
Neurodegener Dis. 2008;5(1):23-6. doi: 10.1159/000109934.
Monoclonal antibodies against a variety of receptors and molecules are currently being introduced in clinical medicine. One of these targets is the interleukin-2 receptor alpha-chain CD25. The humanized monoclonal anti-CD25 antibody daclizumab (Zenapax) has been approved several years ago for the prevention of allotransplant rejection and adult T cell leukemia. Following promising observations in uveitis, daclizumab has been tested in a number of small clinical trials in multiple sclerosis based on the rationale that blocking CD25 would prevent the expansion of autoreactive T lymphocytes. The data from this preliminary clinical exploration as well as findings about the mechanism of action of anti-CD25 treatment are summarized in this study.
目前,针对多种受体和分子的单克隆抗体正被引入临床医学。其中一个靶点是白细胞介素-2受体α链CD25。人源化抗CD25单克隆抗体达利珠单抗(赛尼哌)已于数年前获批用于预防同种异体移植排斥反应及成人T细胞白血病。在葡萄膜炎的观察结果令人鼓舞之后,基于阻断CD25可防止自身反应性T淋巴细胞扩增的理论,达利珠单抗已在多项针对多发性硬化症的小型临床试验中进行了测试。本研究总结了这一初步临床探索的数据以及抗CD25治疗作用机制的相关发现。