Silverman G J, Carson D A, Patrick K, Vaughan J H, Fong S
Clin Immunol Immunopathol. 1987 Jun;43(3):403-11. doi: 10.1016/0090-1229(87)90150-4.
The mouse monoclonal antibody 17.109 recognizes a cross-reactive idiotype (CRI) associated with kappa IIIb light chains of human IgM-rheumatoid factor (RF) paraproteins. The 17.109 idiotypic determinant is encoded by one or a group of closely related V kappa genes. The association of the idiotype with IgM- and IgA-rheumatoid factors in certain autoimmune diseases necessitates an understanding of how human B lymphocytes can be induced to express the idiotype. To investigate the cellular expression of the 17.109 CRI, peripheral blood lymphocytes from normal donors were stimulated in vitro with Epstein-Barr virus (EBV) and pokeweed mitogen (PWM). EBV induced greater expression of IgM-associated 17.109 CRI than did PWM. The 17.109 CRI was preferentially associated with IgM rather than with IgG. In vivo EBV infection was studied in college students with infectious mononucleosis and displayed similar elevation of IgM-associated 17.109 CRI in sera obtained at presentation of clinical illness. Later, IgM levels declined while IgG-associated 17.109 CRI rose. The 17.109 idiotype was unrelated to antibodies against the Epstein-Barr virus nuclear antigen and the viral capsid antigen and was probably due to generalized activation of early B cells. These observations support the hypothesis that the 17.109 CRI is expressed by in vitro and in vivo EBV-infected cells. The 17.109 idiotype identifies a highly conserved V kappa gene product, which is expressed preferentially after EBV infection, but not exclusively with RF autoantibodies.
小鼠单克隆抗体17.109识别一种与人类IgM类风湿因子(RF)副蛋白的κIIIb轻链相关的交叉反应独特型(CRI)。17.109独特型决定簇由一个或一组密切相关的Vκ基因编码。在某些自身免疫性疾病中,独特型与IgM和IgA类风湿因子的关联使得有必要了解人类B淋巴细胞如何被诱导表达该独特型。为了研究17.109 CRI的细胞表达,来自正常供体的外周血淋巴细胞在体外被爱泼斯坦-巴尔病毒(EBV)和商陆有丝分裂原(PWM)刺激。与PWM相比,EBV诱导了更高水平的与IgM相关的17.109 CRI表达。17.109 CRI优先与IgM相关,而非与IgG相关。对患有传染性单核细胞增多症的大学生进行了体内EBV感染研究,结果显示在临床疾病出现时采集的血清中,与IgM相关的17.109 CRI有类似升高。随后,IgM水平下降,而与IgG相关的17.109 CRI上升。17.109独特型与抗爱泼斯坦-巴尔病毒核抗原和病毒衣壳抗原的抗体无关,可能是由于早期B细胞的普遍激活所致。这些观察结果支持了以下假设:17.109 CRI由体外和体内EBV感染的细胞表达。17.109独特型识别一种高度保守的Vκ基因产物,该产物在EBV感染后优先表达,但并非仅与RF自身抗体相关。