Haigwood N L, Shuster J R, Moore G K, Lee H, Skiles P V, Higgins K W, Barr P J, George-Nascimento C, Steimer K S
Chiron Research Laboratories, Chiron Corporation, Emeryville, CA 94608.
AIDS Res Hum Retroviruses. 1990 Jul;6(7):855-69. doi: 10.1089/aid.1990.6.855.
Variants of the envelope gene of the HIV-SF2 isolate of HIV-1 with deletions of one or more of the hypervariable domains of gp120 were produced in genetically engineered yeast as nonglycosylated denatured polypeptide analogs of gp120. Purified antigens were used to immunize experimental animals to determine whether the removal of hypervariable regions from this type of gp120 immunogen had any effect on (1) the ability of the antigen to elicit virus neutralizing antibodies; and (2) the isolate specificity of the neutralizing antibodies that were elicited. The results of these studies demonstrate that, in addition to the previously identified V3 domain, at least two other hypervariable regions in gp120 are capable of eliciting neutralizing antibodies in experimental animals. However, when all five of the hypervariable regions were deleted, the resulting antigen was no longer capable of eliciting neutralizing antibodies. Finally, the neutralizing antibodies elicited by all of these nonglycosylated antigens were effective against HIV-SF2, the isolate from which the antigens were derived, but were not able to neutralize two divergent isolates, HIV-BRU or HIV-Zr6.
在基因工程酵母中产生了HIV-1的HIV-SF2分离株包膜基因的变体,这些变体缺失了gp120一个或多个高变区,作为gp120的非糖基化变性多肽类似物。使用纯化的抗原来免疫实验动物,以确定从这种类型的gp120免疫原中去除高变区是否对以下方面有任何影响:(1)抗原引发病毒中和抗体的能力;以及(2)所引发的中和抗体的分离株特异性。这些研究结果表明,除了先前确定的V3结构域外,gp120中至少还有另外两个高变区能够在实验动物中引发中和抗体。然而,当所有五个高变区都被删除时,所得抗原不再能够引发中和抗体。最后,所有这些非糖基化抗原所引发的中和抗体对产生这些抗原的HIV-SF2分离株有效,但不能中和另外两个不同的分离株HIV-BRU或HIV-Zr6。