Serban D, Rordorf-Adam C, Sun Y Z, Gordon J
J Immunol. 1985 Nov;135(5):3122-7.
Six anti-DNA hybridoma autoantibodies were prepared by fusing spleen cells from unimmunized MRL/MpJ/lpr/lpr female mice with BALB/c myeloma cells. The monoclonal antibodies were analyzed by solid-phase ELISA for antigen-binding specificities. Three antibodies (62A2, 85A5, and 43B2) bound ssDNA, TNP-KLH, and recognized an epitope(s) present on insolubilized proteins such as BSA, KLH, ferritin, and insulin. The antibodies bound, with a marked preference, TNP-KLH, either soluble or insoluble. The other three antibodies (35A1, 32C5, and 39D2) bound only ssDNA. However, this binding was inhibited by free flavinic acid. None of the six antibodies bound either cardiolipin or proteoglycans, indicating that they do not recognize the repeating negatively charge units common to cardiolipin, proteoglycans, and DNA. All six monoclonal antibodies were purified by affinity chromatography with TNP-Sepharose. Moreover, both anti-DNA and anti-TNP antibodies from sera of nonautoimmune and autoimmune mice were purified easily on TNP-Sepharose.
通过将未免疫的MRL/MpJ/lpr/lpr雌性小鼠的脾细胞与BALB/c骨髓瘤细胞融合,制备了六种抗DNA杂交瘤自身抗体。通过固相ELISA分析单克隆抗体的抗原结合特异性。三种抗体(62A2、85A5和43B2)结合单链DNA、TNP-KLH,并识别存在于不溶性蛋白质(如牛血清白蛋白、钥孔戚血蓝蛋白、铁蛋白和胰岛素)上的一个或多个表位。这些抗体明显更倾向于结合可溶性或不溶性的TNP-KLH。另外三种抗体(35A1、32C5和39D2)仅结合单链DNA。然而,这种结合被游离的黄素酸抑制。这六种抗体均不结合心磷脂或蛋白聚糖,表明它们不识别心磷脂、蛋白聚糖和DNA共有的重复负电荷单元。所有六种单克隆抗体均通过用TNP-琼脂糖进行亲和层析纯化。此外,来自非自身免疫和自身免疫小鼠血清的抗DNA和抗TNP抗体都能很容易地在TNP-琼脂糖上纯化。