Bologa L, Hofstetter W, Schonenberger K, Jacque C, Herschkowitz N
Neurochem Res. 1985 Apr;10(4):469-81. doi: 10.1007/BF00964651.
A double ligand enzyme-linked immunosorbent assay (ELISA) has been developed to detect antibodies against brain tissue antigens in the sera of patients with neurological diseases. The sera were tested on human white matter homogenate. The technique consists of successive incubations with the human serum to be tested, rabbit immunoglobulin G (IgG) to human immunoglobulins (Ig), alkaline phosphate-labeled protein A and alkaline phosphatase substrate. This procedure has the advantage of increased sensitivity compared to the classical ELISA. Application of this procedure to the sera of patients with neurological diseases showed that the unspecific binding is very low and the results are reliable. Moreover the test allows the detection of antibodies to chemically different antigenic structures that can occur in a variety of neurological diseases.
已开发出一种双配体酶联免疫吸附测定法(ELISA),用于检测神经疾病患者血清中针对脑组织抗原的抗体。在人白质匀浆上对血清进行检测。该技术包括依次与待测人血清、针对人免疫球蛋白(Ig)的兔免疫球蛋白G(IgG)、碱性磷酸酶标记的蛋白A和碱性磷酸酶底物进行孵育。与经典ELISA相比,该方法具有更高的灵敏度。将此方法应用于神经疾病患者的血清表明,非特异性结合非常低,结果可靠。此外,该检测方法能够检测出多种神经疾病中可能出现的针对化学结构不同的抗原性结构的抗体。