Horneff G, Emmrich F, Burmester G R
Department of Paediatrics, University of Düsseldorf, Germany.
Br J Rheumatol. 1993 Jun;32 Suppl 4:39-47. doi: 10.1093/rheumatology/32.suppl_4.39.
Rheumatoid arthritis is a chronic inflammatory disease mainly affecting the joints. The etiology of the disease is still unknown, but it shows several of the clinical and laboratory features of an autoimmune process. Often, efficacy of conventional treatment is not satisfactory in patients with RA and therefore, alternative therapies have to be considered. Since CD4+ T helper cells appear to play an important role in disease pathogenesis, anti-CD4 treatment has been tried in RA patients. This paper will present a summary of our experience including some new recent findings upon immunomodulation caused by anti-CD4. Following anti-CD4 antibody infusion with antibody MAX16H5, a decline in lymphocyte counts has been observed with a depletion of CD3+ T cells to 30%, CD4+ T cells to 13% and monocytes to 33% of pretreatment levels. Moreover, all remaining T helper cells were coated by anti-CD4. No changes in CD8+ T cells or B lymphocytes were noted. After a partial recovery of CD4+ T cells, decreased numbers were maintained for 8 weeks. Modulation of the target antigen was demonstrated by high levels of soluble CD4 and a decreased CD4 antigen density on T helper cells down to 30% of the original level, which reached pretreatment levels 2 weeks after therapy. Proliferative responses to mitogens and antigens were reduced immediately after the antibody infusions but were markedly increased in some patients when compared to the pretreatment situation. In addition, a rapid decrease of monocyte/macrophage activation markers was observed.(ABSTRACT TRUNCATED AT 250 WORDS)
类风湿性关节炎是一种主要影响关节的慢性炎症性疾病。该疾病的病因仍不清楚,但它表现出自身免疫过程的一些临床和实验室特征。通常,常规治疗对类风湿性关节炎患者的疗效并不令人满意,因此必须考虑替代疗法。由于CD4 + T辅助细胞似乎在疾病发病机制中起重要作用,因此已在类风湿性关节炎患者中尝试进行抗CD4治疗。本文将总结我们的经验,包括一些关于抗CD4引起的免疫调节的最新发现。在用抗体MAX16H5输注抗CD4抗体后,观察到淋巴细胞计数下降,CD3 + T细胞耗竭至预处理水平的30%,CD4 + T细胞耗竭至13%,单核细胞耗竭至33%。此外,所有剩余的T辅助细胞均被抗CD4包被。未观察到CD8 + T细胞或B淋巴细胞的变化。在CD4 + T细胞部分恢复后,数量减少持续了8周。高水平的可溶性CD4和T辅助细胞上CD4抗原密度降低至原始水平的30%,证明了靶抗原的调节,该水平在治疗后2周达到预处理水平。抗体输注后,对丝裂原和抗原的增殖反应立即降低,但与预处理情况相比,一些患者的增殖反应明显增加。此外,观察到单核细胞/巨噬细胞激活标志物迅速下降。(摘要截短至250字)