UMR CNRS 7211, INSERM U959, Groupe Hospitalier Pitié-Salpetrière, and Université Pierre et Marie Curie, Paris 6, Paris, France.
Arthritis Rheumatol. 2014 Feb;66(2):433-43. doi: 10.1002/art.38222.
Hepatitis C virus (HCV) is associated with B cell lymphoproliferative disorders, including mixed cryoglobulinemia (MC) vasculitis and B cell non-Hodgkin's lymphoma. The expansion of clonal and autoreactive rheumatoid factor-bearing CD21(-/low) marginal zone (MZ) B cells was demonstrated in patients with HCV-associated MC vasculitis. Fc receptor-like (FCRL) proteins comprise a family of immunoregulatory proteins preferentially expressed on B lineage cells. The goal of this study was to investigate the expression of FCRL proteins 1-5 on B cells from patients with HCV-associated MC vasculitis.
Expression of FCRL proteins 1-5 was assessed by flow cytometry on B cells from 15 HCV-infected patients with type II MC (7 of whom had B cell non-Hodgkin's lymphoma), 20 HCV-infected patients without MC, and 20 healthy donors. To evaluate FCRL-5 as an immunotherapy target in HCV-associated MC vasculitis, 2 anti-FCRL-5 recombinant immunotoxins were produced using anti-FCRL-5 monoclonal antibodies and Pseudomonas exotoxin.
Expression of FCRLs 2, 3, and 5 was markedly increased while expression of FCRL-1 was decreased on clonal CD21(-/low) MZ B cells, as compared with other B cell subsets, from HCV-infected patients and healthy donors. However, there was no difference in the pattern of FCRL expression between HCV-MC patients with lymphoma and those without lymphoma. The anti-FCRL-5 immunotoxins showed specific cytotoxicity against FCRL-5-expressing clonal CD21(-/low) MZ B cells isolated from HCV-infected patients as well as FCRL-5-transfected cell lines. No cytotoxicity against T cells or conventional B cells was observed.
These findings suggest that FCRL-5-targeting therapies could be a specific treatment for HCV-associated MC vasculitis and other FCRL-5-positive autoimmune B cell disorders.
丙型肝炎病毒(HCV)与 B 细胞淋巴增生性疾病有关,包括混合性冷球蛋白血症(MC)血管炎和 B 细胞非霍奇金淋巴瘤。在丙型肝炎病毒相关 MC 血管炎患者中,已证明克隆和自身反应性类风湿因子携带的 CD21(-/低)边缘区(MZ)B 细胞的扩增。Fc 受体样(FCRL)蛋白家族是一组优先在 B 细胞谱系细胞上表达的免疫调节蛋白。本研究的目的是研究 FCRL 蛋白 1-5 在丙型肝炎病毒相关 MC 血管炎患者的 B 细胞上的表达。
通过流式细胞术评估 15 例丙型肝炎病毒感染的 II 型 MC 患者(其中 7 例患有 B 细胞非霍奇金淋巴瘤)、20 例丙型肝炎病毒感染无 MC 患者和 20 例健康供者的 B 细胞上 FCRL 蛋白 1-5 的表达。为了评估 FCRL-5 作为丙型肝炎病毒相关 MC 血管炎的免疫治疗靶点,使用抗 FCRL-5 单克隆抗体和铜绿假单胞菌外毒素制备了 2 种抗 FCRL-5 重组免疫毒素。
与其他 B 细胞亚群相比,丙型肝炎病毒感染者和健康供者的克隆性 CD21(-/低)MZ B 细胞上 FCRLs 2、3 和 5 的表达明显增加,而 FCRL-1 的表达减少。然而,在患有淋巴瘤和不患有淋巴瘤的丙型肝炎病毒-MC 患者之间,FCRL 表达模式没有差异。抗 FCRL-5 免疫毒素对从丙型肝炎病毒感染者分离的克隆性 CD21(-/低)MZ B 细胞以及 FCRL-5 转染细胞系具有特异性细胞毒性。未观察到对 T 细胞或常规 B 细胞的细胞毒性。
这些发现表明,FCRL-5 靶向治疗可能是丙型肝炎病毒相关 MC 血管炎和其他 FCRL-5 阳性自身免疫性 B 细胞疾病的特异性治疗方法。