Thomssen R, Bonk S, Thiele A
Department of Medical Microbiology, University of Göttingen, Germany.
Med Microbiol Immunol. 1993 Dec;182(6):329-34. doi: 10.1007/BF00191948.
Heterogeneities in the density of hepatitis C virus RNA-carrying material (HCV-RNA-CM) found in human sera (1.03-1.20 g/cm3) are attributed to the binding of low-density lipoproteins and/or of IgG. In some sera HCV-RNA-CM seems to be nearly totally bound to beta-lipoproteins and cannot be precipitated by anti-IgG (gamma); in others more than 95% of HCV-RNA-CM is bound to IgG and cannot be precipitated by anti-beta-lipoprotein. Furthermore, there are sera from which HCV-RNA-CM can be completely be precipitated by either anti-beta-lipoprotein or anti-IgG (gamma), pointing to a binding of the two serum proteins to the same HCV-RNA-CM. There are other sera from which HCV-RNA-CM can be partially precipitated by the one or the other antiserum, leaving behind fractions, which are bound to beta-lipoprotein or to IgG. HCV-RNA-CM cannot be precipitated from some sera either by anti-beta-lipoprotein or by anti-IgG (gamma).
在人血清(1.03 - 1.20克/立方厘米)中发现的携带丙型肝炎病毒RNA物质(HCV - RNA - CM)密度的异质性归因于低密度脂蛋白和/或IgG的结合。在某些血清中,HCV - RNA - CM似乎几乎完全与β - 脂蛋白结合,不能被抗IgG(γ)沉淀;在其他血清中,超过95%的HCV - RNA - CM与IgG结合,不能被抗β - 脂蛋白沉淀。此外,有些血清中的HCV - RNA - CM可以被抗β - 脂蛋白或抗IgG(γ)完全沉淀,这表明这两种血清蛋白与同一HCV - RNA - CM结合。还有其他血清,其中的HCV - RNA - CM可以被其中一种抗血清部分沉淀,剩余部分则与β - 脂蛋白或IgG结合。有些血清中的HCV - RNA - CM既不能被抗β - 脂蛋白沉淀,也不能被抗IgG(γ)沉淀。