Berkower I, Smith G E, Giri C, Murphy D
Division of Biochemistry and Biophysics, Food and Drug Administration, Bethesda, Maryland 20892.
J Exp Med. 1989 Nov 1;170(5):1681-95. doi: 10.1084/jem.170.5.1681.
HIV-1 is known to show a high degree of genetic diversity, which may have major implications for disease pathogenesis and prevention. If every divergent isolate represented a distinct serotype, then effective vaccination might be impossible. However, using a sensitive new plaque-forming assay for HIV-1, we have found that most infected patients make neutralizing antibodies, predominantly to a group-specific epitope shared among three highly divergent isolates. This epitope persists among divergent isolates and rarely mutates, despite the rapid overall mutation rate of HIV-1, suggesting that it may participate in an essential viral function. These findings, plus the rarity of reinfections among these patients, suggest that HIV-1 may be more susceptible to a vaccine strategy based on a group-specific neutralizing epitope than was previously suspected.
众所周知,HIV-1具有高度的遗传多样性,这可能对疾病的发病机制和预防产生重大影响。如果每一个不同的分离株都代表一种独特的血清型,那么有效的疫苗接种可能是不可能的。然而,通过使用一种针对HIV-1的敏感的新噬斑形成试验,我们发现大多数感染患者会产生中和抗体,主要针对三种高度不同的分离株中共同存在的一个组特异性表位。尽管HIV-1总体突变率很快,但这个表位在不同的分离株中持续存在且很少发生突变,这表明它可能参与了病毒的一种基本功能。这些发现,再加上这些患者再次感染的罕见性,表明HIV-1可能比以前认为的更容易受到基于组特异性中和表位的疫苗策略的影响。