McPherson T A, Marchalonis J J, Lennon V
Immunology. 1970 Dec;19(6):929-33.
The binding capacity of human and rabbit serum and serum fractions for [I]encephalitogenic basic protein, extracted from human brain, were determined by gel-filtration radioimmunoassay. Strong binding was effected by the γ-globulin fraction or whole serum of a rabbit with experimental allergic encephalitis, and was completely inhibited by excess of unlabelled encephalitogenic basic protein but not by large amounts of lysozyme. Smaller amounts of encephalitogenic basic protein were bound by normal rabbit and human serum, and by the serum of a patient with multiple sclerosis: the α-macroglobulin fraction was responsible for this, and complete inhibition was effected by excess unlabelled encephalitogenic basic protein but only partial inhibition by excess lysozyme. It is concluded that binding detected in some radioimmunoassay systems may not represent a classical antigen—antibody reaction, and it is suggested that α-macroglobulins may, by binding , be of importance in experimental allergic encephalomyelitis and, by analogy, in human demyelinating disease.
采用凝胶过滤放射免疫分析法测定了人和兔血清及血清组分对从人脑中提取的[I]致脑炎碱性蛋白的结合能力。患有实验性变应性脑脊髓炎的兔的γ球蛋白组分或全血清具有较强的结合作用,且这种结合作用可被过量的未标记致脑炎碱性蛋白完全抑制,但不能被大量溶菌酶抑制。正常兔和人血清以及一名多发性硬化症患者的血清对致脑炎碱性蛋白的结合量较少:α巨球蛋白组分起了这一作用,过量的未标记致脑炎碱性蛋白可完全抑制结合,而过量溶菌酶只能部分抑制结合。得出的结论是,在某些放射免疫分析系统中检测到的结合可能并不代表经典的抗原-抗体反应,并且有人提出,α巨球蛋白可能通过结合作用在实验性变应性脑脊髓炎中起重要作用,类推而言,在人类脱髓鞘疾病中也起重要作用。