Moore J P, Cao Y, Leu J, Qin L, Korber B, Ho D D
Aaron Diamond AIDS Research Center, New York University School of Medicine, New York 10016, USA.
J Virol. 1996 Jan;70(1):427-44. doi: 10.1128/JVI.70.1.427-444.1996.
We have studied genetic variation among clades A through E of human immunodeficiency virus type 1 (HIV-1) at the levels of antibody binding to gp120 molecules and virus neutralization. We are unable to identify neutralization serotypes that correspond to the genetic clades. Instead, we observe that inter- and intraclade neutralization of primary isolates by HIV-1-positive sera is generally weak and sporadic; some sera show a reasonable degree of neutralization breadth and potency whereas others are relatively sensitive to neutralization, but no consistent pattern was found. However, a few sera were able to neutralize across clades with significant potency, an observation which may have implications for the feasibility of a broadly effective HIV-1 vaccine involving humoral immunity. Serological assays measuring anti-gp120 antibody binding also failed to identify serotypes that correspond precisely to the genetic clades, but some indications of clade-specific binding were observed, notably with sera from clades B and E. A representative protein for each clade (A through E) was selected on the basis of its specificity, defined as high seroreactivity with sera from individuals infected with virus of that clade and lower reactivity with sera from individuals infected with viruses from other clades. The seroreactivity patterns against these five proteins could be used to predict the genotype of the infecting virus with moderate success.
我们已经在抗体与gp120分子结合及病毒中和水平上研究了1型人类免疫缺陷病毒(HIV-1)A至E各进化枝间的基因变异。我们无法识别与基因进化枝相对应的中和血清型。相反,我们观察到HIV-1阳性血清对原代分离株的进化枝间和进化枝内中和作用通常较弱且不连续;一些血清显示出合理程度的中和广度和效力,而另一些则对中和作用相对敏感,但未发现一致的模式。然而,少数血清能够高效中和不同进化枝的病毒,这一观察结果可能对涉及体液免疫的广泛有效的HIV-1疫苗的可行性具有启示意义。检测抗gp120抗体结合的血清学检测也未能识别出与基因进化枝精确对应的血清型,但观察到了一些进化枝特异性结合的迹象,特别是来自B和E进化枝的血清。根据其特异性,为每个进化枝(A至E)选择了一种代表性蛋白质,其定义为与感染该进化枝病毒的个体血清具有高血清反应性,而与感染其他进化枝病毒的个体血清反应性较低。针对这五种蛋白质的血清反应模式可用于以一定的成功率预测感染病毒的基因型。