Rheumatology Unit, Department of Internal Medicine, University of Modena e Reggio Emilia, Medical School, Via del Pozzo 71, Modena, Italy.
Autoimmun Rev. 2011 Nov;11(1):48-55. doi: 10.1016/j.autrev.2011.07.005. Epub 2011 Jul 24.
Mixed cryoglobulinemia syndrome (MCs) is a systemic vasculitis characterized by multiple organ involvement due to the vascular deposition of immune-complexes, mainly the cryoglobulins. B-lymphocyte expansion represents the underlying pathological alteration frequently triggered by hepatitis C virus (HCV) infection. The treatment of MCs syndrome is generally based on antiviral drugs and/or immunosuppressors, among which rituximab, an anti-CD20 monoclonal antibody, has been usefully employed for both cutaneous and visceral MCs organ involvement. This multicenter study retrospectively evaluated the effects of rituximab in a large series of patients with active MCs. The observed results were compared to those emerging from the updated review of the literature on this topic.
The study included 87 patients (male/female 19/68, mean age 62.3±11.4SD years, mean disease duration 9±6.2SD years, HCV infection in 92% of cases) with active cryoglobulinemic vasculitis evaluated before rituximab monotherapy and after 6-month follow-up by means of main clinico-serological parameters. A PubMed search up to May 31, 2011, was done to find published clinical studies, including case reports of MCs treated with rituximab.
A significant clinical improvement was observed in a relevant percentage of cases, regardless the presence/absence of associated HCV infection; namely, complete/partial remission of pre-treatment active manifestations was observed in 74% of skin purpuric lesions, up to 87% of non-healing vasculitic leg ulcers, and 44% of the peripheral neuropathy, mainly paresthesias (patient's visual analogical scale from 62±25 to 37±27; p≤.0001). Moreover, cryoglobulinemic nephropathy, observed in 38 patients, significantly improved in 95% of cases (serum creatinine from 1.8±1.1SD to 1.4±0.8SD mg/dl, p≤.0001; 24-hour proteinuria from 2.2±2.1SD to 0.9±1.7SD g/24h, p≤.0001), with complete remission in the 50%. Among 6 patients with complicating non-Hodgkin's B-cell lymphoma a complete or partial remission was observed in 5/6. A complete remission of abdominal vasculitis was also observed in one patient. These beneficial effects were mirrored by the improvement of cryoglobulinemic serological hallmarks, namely cryocrit and low complement C4, in half cases. The safety of rituximab was confirmed by the small number of side effects recorded during the 6-month follow-up. On the whole, the results of the present study are in keeping with those reported in 39 papers present in world literature, including a total of 279 MCs patients.
Rituximab may be regarded as useful and safe pathogenetic treatment of cryoglobulinemic vasculitis. The actual role of this drug should be definitely confirmed by randomized controlled trials, as well as its position in the therapeutical strategy, mainly with respect to antiviral treatment in HCV-associated MCs.
混合性冷球蛋白血症综合征(MCs)是一种系统性血管炎,其特征是由于免疫复合物(主要是冷球蛋白)在血管中的沉积,导致多个器官受累。B 淋巴细胞的扩增代表了经常由丙型肝炎病毒(HCV)感染引发的潜在病理改变。MCs 综合征的治疗通常基于抗病毒药物和/或免疫抑制剂,其中利妥昔单抗,一种抗 CD20 的单克隆抗体,已被用于治疗皮肤和内脏 MCs 器官受累。这项多中心研究回顾性评估了利妥昔单抗在一系列活动性 MCs 患者中的疗效。观察到的结果与该主题的文献更新综述中出现的结果进行了比较。
这项研究纳入了 87 例(男/女 19/68 例,平均年龄 62.3±11.4 岁,平均病程 9±6.2 年,92%的病例存在 HCV 感染)患有活动性冷球蛋白血症性血管炎的患者,在接受利妥昔单抗单药治疗前和 6 个月随访时,通过主要临床血清学参数进行评估。截至 2011 年 5 月 31 日,通过 PubMed 检索了发表的临床研究,包括用利妥昔单抗治疗的 MCs 的病例报告。
无论是否存在相关的 HCV 感染,大多数情况下都观察到显著的临床改善,即治疗前活动性表现的完全/部分缓解,皮肤紫癜病变的缓解率为 74%,未愈合的血管炎性腿部溃疡的缓解率高达 87%,周围神经病的缓解率为 44%,主要是感觉异常(患者的视觉模拟评分从 62±25 降至 37±27;p≤.0001)。此外,38 例观察到冷球蛋白血症性肾病,95%的病例显著改善(血清肌酐从 1.8±1.1SD 降至 1.4±0.8SDmg/dl,p≤.0001;24 小时蛋白尿从 2.2±2.1SD 降至 0.9±1.7SDg/24h,p≤.0001),50%的病例完全缓解。6 例并发非霍奇金 B 细胞淋巴瘤的患者中,有 5 例观察到完全或部分缓解。1 例腹部血管炎也完全缓解。这些有益的效果反映在冷球蛋白血症血清学标志物的改善上,即冷沉淀和低补体 C4 的改善,在一半的病例中。利妥昔单抗的安全性通过在 6 个月随访期间记录的少量副作用得到证实。总的来说,本研究的结果与世界文献中 39 篇论文报告的结果一致,包括 279 例 MCs 患者。
利妥昔单抗可被视为治疗冷球蛋白血症性血管炎的有效且安全的病因治疗方法。这种药物的实际作用应通过随机对照试验来明确证实,以及在治疗策略中的定位,特别是在 HCV 相关 MCs 的抗病毒治疗方面。