Wendling D, Racadot E, Morel-Fourrier B, Wijdenes J
Service de Rhumatologie, Hôpital J. Minjoz, Besançon, France.
Clin Rheumatol. 1992 Dec;11(4):542-7. doi: 10.1007/BF02283116.
Twenty-five defined severe RA patients (pts) (17 F, 8 M) were treated in an open study with a CD4 murine monoclonal antibody (Mab) (B-F5 clone, IgG1). Mab's daily dose was 10 mg (1 pt), 15 mg (2 pts), 20 mg (17 pts), 30 mg (4 pts) and 50 mg (1 pt) for 10 days. Tolerance was fair. Clinical improvement occurred during treatment period or within the first month in all but 2 patients, irrespective of Mab dosage. Improvement duration was variable (1 to 12 months), half of the patients still show signs of improvement at month 4. Biological parameters (CRP) improved parallel to the clinical. At day 180, 25% of the patients showed a reduction of 50% or more of the initial CRP values. There is no modification of RF titers, renal and hepatic parameters. Sequential evaluation showed a decrease of B, TCD3, CD4, CD8 lymphocytes and monocytes two hours after Mab infusion and return to baseline in 20 hours. Xenogenic immunization occurred in 6 patients without influence upon clinical response. These modifications are moderate and transient and do not account for the more prolonged effect in some cases, nor do they offer any prediction of further clinical response.
25例确诊的重度类风湿关节炎患者(17例女性,8例男性)参与了一项开放性研究,接受一种CD4鼠单克隆抗体(Mab)(B-F5克隆,IgG1)治疗。Mab的每日剂量分别为10mg(1例患者)、15mg(2例患者)、20mg(17例患者)、30mg(4例患者)和50mg(1例患者),持续治疗10天。耐受性良好。除2例患者外,所有患者在治疗期间或第一个月内均出现临床改善,与Mab剂量无关。改善持续时间各不相同(1至12个月),4个月时仍有一半患者显示改善迹象。生物学参数(CRP)与临床情况平行改善。在第180天时,25%的患者初始CRP值降低了50%或更多。类风湿因子滴度、肾和肝参数无变化。连续评估显示,Mab输注后两小时,B细胞、TCD3、CD4、CD8淋巴细胞和单核细胞数量减少,20小时后恢复至基线水平。6例患者发生了异种免疫,但对临床反应无影响。这些变化是中度且短暂的,既不能解释某些情况下更持久的疗效,也无法预测进一步的临床反应。