Traunecker A, Lüke W, Karjalainen K
Basel Institute for Immunology, Switzerland.
Nature. 1988 Jan 7;331(6151):84-6. doi: 10.1038/331084a0.
Human immunodeficiency virus (HIV) infection can bring about total collapse of the immune system by infecting helper T lymphocytes which express CD4, the molecule which mediates interaction between the cell surface and viral envelope glycoprotein gp120 (refs 3-10). HIV apparently escapes the effects of neutralizing antibodies in vivo by generating new variants which must still interact with CD4 to maintain a cycle of infection. One route to block HIV infection, therefore, could use solubilized CD4 protein to inhibit attachment of the virus to its target cell. We have used recombinant DNA techniques to generate soluble forms of CD4, and show here that these are potent inhibitors of HIV infection in vitro.
人类免疫缺陷病毒(HIV)感染可通过感染表达CD4的辅助性T淋巴细胞导致免疫系统完全崩溃,CD4是介导细胞表面与病毒包膜糖蛋白gp120相互作用的分子(参考文献3 - 10)。HIV显然通过产生新的变体在体内逃避中和抗体的作用,这些新变体仍必须与CD4相互作用以维持感染循环。因此,一种阻断HIV感染的途径可以是使用可溶性CD4蛋白来抑制病毒与其靶细胞的附着。我们利用重组DNA技术生成了可溶性形式的CD4,并在此表明这些在体外是HIV感染的有效抑制剂。