Boyer C M, Eisenberg R A, Cohen P L
Arthritis Rheum. 1985 Mar;28(3):294-9. doi: 10.1002/art.1780280309.
Anti-Sm antibodies are specific for the diagnosis of systemic lupus erythematosus both in humans and in mice. Because the autoantibody response to this nuclear ribonucleoprotein particle is probably antigen driven, we have quantitated the Sm antigen in cells and tissues, using a highly sensitive and specific enzyme-linked immunosorbent assay. The Sm content of several in vitro cell lines was determined to be approximately 1 pg of Sm/cell. We found that murine spleen cells stimulated in vitro with either T cell or B cell mitogens contained up to 10 times more Sm than did unstimulated cells and that they also released increased amounts of Sm. In a survey of organs from several mouse strains, we found that lymphoid tissues had the largest amounts of Sm and that the Sm content of a particular tissue correlated with its DNA content. Increased amounts of Sm in and around activated lymphocytes, as found in systemic lupus erythematosus, may provide a source of antigen for the induction of the anti-Sm autoantibody.
抗Sm抗体对人类和小鼠系统性红斑狼疮的诊断具有特异性。由于针对这种核糖核蛋白颗粒的自身抗体反应可能是由抗原驱动的,我们使用高度灵敏且特异的酶联免疫吸附测定法对细胞和组织中的Sm抗原进行了定量。几种体外细胞系的Sm含量测定为约1 pg Sm/细胞。我们发现,用T细胞或B细胞有丝分裂原体外刺激的小鼠脾细胞所含的Sm比未刺激的细胞多多达10倍,并且它们还释放出更多的Sm。在对几种小鼠品系的器官进行的调查中,我们发现淋巴组织中的Sm含量最高,并且特定组织的Sm含量与其DNA含量相关。如在系统性红斑狼疮中所发现的,活化淋巴细胞内外Sm含量的增加可能为抗Sm自身抗体的诱导提供抗原来源。