Yang Lixin, Hakoda Masayuki, Iwabuchi Kazuya, Takeda Tsuyoshi, Koike Takao, Kamatani Naoyuki, Takada Kenzo
Department of Tumor Virology, Institute for Genetic Medicine, Hokkaido University, N15 W7, Kita-ku, Sapporo 060-0815, Japan.
J Virol. 2004 Sep;78(18):9918-23. doi: 10.1128/JVI.78.18.9918-9923.2004.
B-cell antigen receptor signaling is initiated upon binding of the antigen to membrane-bound immunoblobulin (Ig), and the anti-Ig antibody (Ab) mimics this signaling. In B cells latently infected with Epstein-Barr virus (EBV), the same signals induce virus activation. We examine here whether rheumatoid factors (RFs), autoantibodies directed against the Fc portion of IgG, induce EBV and B-cell activation. As a source of RFs, RF-producing lymphoblastoid cell line (LCL) clones were isolated from peripheral blood mononuclear cells (PBMC) and synovial cells from patients with rheumatoid arthritis (RA) by EBV transformation. Burkitt's lymphoma-derived Akata cells, which are highly responsive to EBV activation by anti-Ig Abs, were used for the assay of EBV activation. Akata cells expressed IgG3 as membrane-bound Ig. RFs from a synovium-derived LCL were directed to IgG3 and induced EBV activation in 16 to 18% of Akata cells, whereas RFs from another synovium-derived LCL were directed to IgG1 and did not induce EBV activation. Pretreatment of RFs with the purified Fc fragment of human IgG completely abolished EBV activation. Furthermore, B-cell activation was assessed by incorporation of [3H]thymidine. RFs from synovium-derived LCLs efficiently induced B-cell activation, and the addition of CD40 ligand had a synergistic effect. On the other hand, RFs from PBMC-derived LCLs were polyreactive, had a lower affinity to IgG, and did not induce EBV and B-cell activation. The present findings imply a possible role for RFs as EBV and B-cell activators.
B细胞抗原受体信号传导在抗原与膜结合免疫球蛋白(Ig)结合时启动,抗Ig抗体(Ab)可模拟这种信号传导。在潜伏感染爱泼斯坦-巴尔病毒(EBV)的B细胞中,相同的信号可诱导病毒激活。我们在此研究类风湿因子(RFs),即针对IgG Fc部分的自身抗体,是否会诱导EBV和B细胞激活。作为RFs的来源,通过EBV转化从类风湿关节炎(RA)患者的外周血单核细胞(PBMC)和滑膜细胞中分离出产生RFs的淋巴母细胞样细胞系(LCL)克隆。对通过抗Ig Abs对EBV激活高度敏感的伯基特淋巴瘤衍生的Akata细胞进行EBV激活检测。Akata细胞表达IgG3作为膜结合Ig。来自滑膜来源LCL的RFs靶向IgG3并在16%至18%的Akata细胞中诱导EBV激活,而来自另一个滑膜来源LCL的RFs靶向IgG1且不诱导EBV激活。用人IgG的纯化Fc片段预处理RFs可完全消除EBV激活。此外,通过掺入[3H]胸苷评估B细胞激活。来自滑膜来源LCL的RFs有效诱导B细胞激活,添加CD40配体具有协同作用。另一方面,来自PBMC来源LCL的RFs具有多反应性,对IgG的亲和力较低,且不诱导EBV和B细胞激活。目前的研究结果表明RFs可能作为EBV和B细胞激活剂发挥作用。