Bachelez H, Flageul B, Dubertret L, Fraitag S, Grossman R, Brousse N, Poisson D, Knowles R W, Wacholtz M C, Haverty T P, Chatenoud L, Bach J F
Service Dermatologie, Hôpital Saint-Louis, Paris, France.
J Autoimmun. 1998 Feb;11(1):53-62. doi: 10.1006/jaut.1997.0175.
The presence of activated CD4(+) T lymphocytes in psoriatic skin plaques suggests an immune-mediated pathogenesis for the disease. Six patients with recalcitrant plaque psoriasis (PASI>12) received a humanized non-depleting monoclonal antibody to CD4 (ORTHOCLONE OKT(R)cdr4a). The antibody was well tolerated. Four weeks from treatment, the mean decrease in PASI score was 46%. In three patients disease remission was prolonged for up to 6 months and, in one case, up to 1 year post-treatment. In all patients, circulating CD4+ T-cell counts remained normal and peripheral OKTcdr4a-coated CD4+ lymphocytes were detected up to 10 days after antibody infusion. These results point to the relevance of CD4+ lymphocytes in psoriasis. They also emphasize that depletion of CD4+ cells is not mandatory to achieve therapeutic effectiveness.
银屑病皮肤斑块中活化的CD4(+) T淋巴细胞的存在提示了该疾病的免疫介导发病机制。6例顽固性斑块状银屑病患者(银屑病面积和严重程度指数[PASI]>12)接受了一种人源化的非耗竭性抗CD4单克隆抗体(ORTHOCLONE OKT(R)cdr4a)治疗。该抗体耐受性良好。治疗4周后,PASI评分平均下降46%。3例患者疾病缓解期延长至6个月,1例患者治疗后缓解期长达1年。所有患者循环CD4+ T细胞计数均保持正常,且在抗体输注后长达10天可检测到外周包被OKTcdr4a的CD4+淋巴细胞。这些结果表明CD4+淋巴细胞在银屑病中的相关性。它们还强调,为达到治疗效果并非必须耗竭CD4+细胞。