Zhang Xu, Hupperts Raymond, De Baets Marc
First Affiliated Hospital, Wenzhou Medical College, Wenzhou, PR China.
Immunol Res. 2003;28(1):61-78. doi: 10.1385/IR:28:1:61.
Experimental autoimmune encephalomyelitis (EAE) is a T-cell-mediated demyelinating disease of the central nervous system that has been used as an animal model for multiple sclerosis (MS). Based on the exciting results in EAE, a number of novel immunotherapies employing biotechnological products, rather than conventional immunosuppressants, are being developed for the treatment of MS. In this review, we delineate the rationale for monoclonal antibody (MAb) therapy in EAE and MS and summarize the various levels at which immune intervention was performed. For each approach, we discuss the role of MAbs at the level of lymphocyte and cytokine networks, chemokines, and adhesion molecules or their receptors.
实验性自身免疫性脑脊髓炎(EAE)是一种中枢神经系统的T细胞介导的脱髓鞘疾病,已被用作多发性硬化症(MS)的动物模型。基于EAE中令人振奋的结果,正在开发多种采用生物技术产品而非传统免疫抑制剂的新型免疫疗法来治疗MS。在本综述中,我们阐述了在EAE和MS中进行单克隆抗体(MAb)治疗的基本原理,并总结了进行免疫干预的各个层面。对于每种方法,我们讨论了MAb在淋巴细胞和细胞因子网络、趋化因子以及黏附分子或其受体层面所起的作用。