Langewouters Annechien M G, Van Erp Piet E J, De Jong Elke M G J, Van De Kerkhof Peter C M
Department of Dermatology, Radboud University Nijmegen, Nijmegen, The Netherlands.
J Dermatolog Treat. 2006;17(6):362-9. doi: 10.1080/09546630601028794.
Alefacept is a biologic treatment for psoriasis, with a selective effect on memory effector T cells. Few data are available on the combination of alefacept with either topical or systemic anti-psoriatics. We studied the effect of alefacept combination treatment on clinical disease severity scores and on circulating T-cell subsets.
Twelve patients with moderate-to-severe psoriasis were included and treated with alefacept for a period of 12 weeks. Patients were allowed to continue the anti-psoriatic therapies they used prior to the study. Severity of disease and expression of T-cell markers CD4, CD8, CD45RA, CD45RO, CD94, CD161, CD25, and CLA were assessed at baseline and after treatment.
Seven of 12 included patients used a concomitant systemic therapy: either methotrexate (n = 4), acitretin (n = 2) or cyclosporine (n = 1). PASI reductions in this group after 12 and 24 weeks were 40% and 55%, respectively. Several lymphocyte subsets showed a reduction in circulating numbers. These decreases were independent of the use of an additional systemic psoriasis therapy.
The concomitant use of systemic anti-psoriatic medication in combination with alefacept has a noteworthy impact on efficacy results. No differences in circulating psoriasis-relevant T-cell populations between patients with or without an additional systemic treatment were seen.
阿法赛特是一种用于治疗银屑病的生物制剂,对记忆效应T细胞具有选择性作用。关于阿法赛特与局部或全身性抗银屑病药物联合使用的数据较少。我们研究了阿法赛特联合治疗对临床疾病严重程度评分和循环T细胞亚群的影响。
纳入12例中度至重度银屑病患者,给予阿法赛特治疗12周。患者可继续使用研究前使用的抗银屑病疗法。在基线和治疗后评估疾病严重程度以及T细胞标志物CD4、CD8、CD45RA、CD45RO、CD94、CD161、CD25和CLA的表达。
12例纳入患者中有7例同时使用了全身性疗法:甲氨蝶呤(4例)、阿维A(2例)或环孢素(1例)。该组在12周和24周后的银屑病面积和严重程度指数(PASI)降低分别为40%和55%。几个淋巴细胞亚群的循环数量减少。这些减少与额外使用全身性银屑病疗法无关。
全身性抗银屑病药物与阿法赛特联合使用对疗效结果有显著影响。在使用或未使用额外全身性治疗的患者之间,与银屑病相关的循环T细胞群体未见差异。