Schorlemmer H U, Kanzy E J, Kurrle R, Seiler F R
Research Laboratories of Behringwerke AG, Marburg/Lahn, FRG.
Agents Actions. 1991 Sep;34(1-2):161-4. doi: 10.1007/BF01993266.
The anti-rat alpha/beta-TCR, MAb-R73 has been investigated as to its disease modifying activity on adjuvant arthritis (AA), on experimental allergic encephalomyelitis (EAE) and on a local graft versus host (GvH) reaction (popliteal lymph nodes = PLN) in Lewis or Brown-Norway rats. R73 was able to prevent the onset of the AA and even if therapy started after the establishment of AA the MAb was still able to reduce the degree of chronic inflammation and arrest its progress. Intravenous MAb-R73 application also reduced the signs of EAE and prevented mortality. This was even seen when the substance was given after the outbreak of the clinical symptoms or when the F(ab)2 fragment of this MAb was used. Also in the model of local GvH reaction R73 acted therapeutically and lowered the PLN weights.
抗大鼠α/β -TCR单克隆抗体R73已针对其对佐剂性关节炎(AA)、实验性变应性脑脊髓炎(EAE)以及Lewis或Brown-Norway大鼠局部移植物抗宿主反应(GvH)(腘窝淋巴结=PLN)的疾病修饰活性进行了研究。R73能够预防AA的发作,并且即使在AA确立后开始治疗,该单克隆抗体仍能够减轻慢性炎症的程度并阻止其进展。静脉内应用单克隆抗体R73也减轻了EAE的症状并预防了死亡。当在临床症状发作后给予该物质或使用该单克隆抗体的F(ab)2片段时,也观察到了这种情况。同样在局部GvH反应模型中,R73具有治疗作用并降低了PLN重量。