Stephens John B, Wilkerson Michael G
Department of Dermatology, University of Texas Medical Branch, Galveston, TX 77555, USA.
J Drugs Dermatol. 2011 Feb;10(2):202-5.
Rituximab is a chimeric monoclonal antibody against CD20 that mediates B-cell depletion. It has been shown to be effective in a variety of autoimmune-related diseases, including pemphigus vulgaris. Most reports of pemphigus treatment utilize the weekly dosing regimen designed for the treatment of B-cell malignancy. The authors report a case of successful treatment of refractory pemphigus vulgaris in an adolescent male using three infusions of rituximab spread over a four-month period of time. The authors also discuss recent updates in rituximab's mechanism of action in autoimmune disease. Rituximab acts to destroy auto-reactive B-cells prior to their development into auto-antibody producing plasma cells. More recent reports have shown that rituximab also indirectly leads to a decrease of autoreactive CD4+ T cells via depletion of B-cells that are necessary for antigen presentation. Monthly to bi-monthly rituximab infusion dosing may be a more appropriate dosing strategy for autoimmune disease that minimizes potential side effects while generating remission of disease. Dermatology continues to see an increase in use of medications designed for treatment of rheumatologic disease and malignancy. Additional studies should focus on the appropriate dosing of these medications for dermatologic conditions that limit the risk of adverse effects while preserving therapeutic benefit.
利妥昔单抗是一种针对CD20的嵌合单克隆抗体,可介导B细胞耗竭。已证明它在多种自身免疫相关疾病中有效,包括寻常型天疱疮。大多数天疱疮治疗报告采用为治疗B细胞恶性肿瘤设计的每周给药方案。作者报告了一例青少年男性难治性寻常型天疱疮成功治疗的病例,该病例在四个月的时间内分三次输注利妥昔单抗。作者还讨论了利妥昔单抗在自身免疫性疾病中作用机制的最新进展。利妥昔单抗的作用是在自身反应性B细胞发育成产生自身抗体的浆细胞之前将其破坏。最近的报告表明,利妥昔单抗还通过消耗抗原呈递所需的B细胞间接导致自身反应性CD4+T细胞减少。对于自身免疫性疾病,每月至每两个月输注一次利妥昔单抗可能是一种更合适的给药策略,既能将潜在副作用降至最低,又能使疾病缓解。皮肤科对用于治疗风湿性疾病和恶性肿瘤的药物的使用持续增加。更多研究应关注这些药物在皮肤病中的适当剂量,以在保持治疗效果的同时限制不良反应的风险。