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人类组织相容性决定簇与病毒抗原:麻疹病毒感染对HLA表达的影响

Human histocompatibility determinants and virus antigens: effect of measles virus infection on HLA expression.

作者信息

Haspel M V, Pellegrino M A, Lampert P W, Oldstone M B

出版信息

J Exp Med. 1977 Jul 1;146(1):146-56. doi: 10.1084/jem.146.1.146.

Abstract

Histocompatibility antigens on the surface of human lymphoblastoid cells were quantified by a microadsorption technique. During the course of measles virus infection, no quantitative or qualitations in surface HLA antigens were observed. In contrast, infection with poliovirus type 1 or vesicular stomatitis virus, or treatment with puromycin (50 microgram/ml) resulted in a significant decrease in surface HLA. These experiments suggest that an inhibition of host protein synthesis rather than the insertion of virus-specificied antigens into the membrane results in a net decrease in amounts of this cell surface antigen. The HLA antigens also appear to be both functionally and structurally distinct from measles virus surface antigens. Pretreatment of cells with HLA-directed antibody did not prevent the infection of these cells by measles virus, thus HLA antigens appear unrelated to the measles virus receptor site on the plasma membrane. Electron microscopic studies revealed that measles virus maturation occurs at membrane sites devoid of demonstrable HLA. Furthermore, HLA antigens could not be detected on the surfaces of mature infectious virions.

摘要

通过微量吸附技术对人淋巴母细胞表面的组织相容性抗原进行了定量分析。在麻疹病毒感染过程中,未观察到表面HLA抗原的定量或定性变化。相比之下,感染1型脊髓灰质炎病毒或水疱性口炎病毒,或用嘌呤霉素(50微克/毫升)处理,会导致表面HLA显著减少。这些实验表明,宿主蛋白合成的抑制而非病毒特异性抗原插入细胞膜导致了这种细胞表面抗原量的净减少。HLA抗原在功能和结构上似乎也与麻疹病毒表面抗原不同。用HLA导向抗体对细胞进行预处理并不能阻止麻疹病毒对这些细胞的感染,因此HLA抗原似乎与质膜上的麻疹病毒受体位点无关。电子显微镜研究显示,麻疹病毒成熟发生在缺乏可检测到的HLA的膜位点。此外,在成熟的感染性病毒粒子表面未检测到HLA抗原。

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