Horsfall A C, Venables P J, Mumford P A, Maini R N
Clin Exp Immunol. 1981 May;44(2):405-15.
The Raji cell assay is regarded as a test for the detection and quantitation of immune complexes. It is frequently positive in sera from patients with SLE. We have demonstrated a relationship between Raji cell binding and antibodies to DNA and soluble cellular antigens. In five sera containing high titres of antibodies of known single specificity, most of the Raji cell binding occurred in the 7S IgG fraction where the majority of anti-nuclear antibody was also found. When each of these sera was incubated with its specific antigen, Raji cell binding increased. Subsequent fractionation showed that this binding was in the high molecular weight fraction (greater than 200,000 daltons) and that Raji cell binding and antibody activity were abolished in the 7S fraction. These data confirm that Raji cell bind immune complexes but also indicate that 7S anti-nuclear antibodies may interact directly with Raji cells by an unknown mechanism. Therefore, in sera of patients with anti-nuclear antibodies, binding to Raji cells does not necessarily imply the presence of immune complexes alone.
拉吉细胞试验被视为检测和定量免疫复合物的一种测试方法。它在系统性红斑狼疮患者的血清中常常呈阳性。我们已经证实了拉吉细胞结合与抗DNA抗体及可溶性细胞抗原之间的关系。在五份含有已知单一特异性高滴度抗体的血清中,大多数拉吉细胞结合发生在7S IgG组分中,而大部分抗核抗体也存在于此组分中。当这些血清中的每一份与其特异性抗原孵育时,拉吉细胞结合增加。随后的分级分离表明,这种结合存在于高分子量组分(大于200,000道尔顿)中,并且在7S组分中拉吉细胞结合和抗体活性被消除。这些数据证实拉吉细胞结合免疫复合物,但也表明7S抗核抗体可能通过未知机制直接与拉吉细胞相互作用。因此,在有抗核抗体的患者血清中,与拉吉细胞的结合不一定仅意味着存在免疫复合物。