Prince A M, Reesink H, Pascual D, Horowitz B, Hewlett I, Murthy K K, Cobb K E, Eichberg J W
Lindsley F. Kimball Research Institute, New York Blood Center, NY 10021.
AIDS Res Hum Retroviruses. 1991 Dec;7(12):971-3. doi: 10.1089/aid.1991.7.971.
The use of a human immunodeficiency virus (HIV) immune globulin (HIVIG) in prevention of HIV infection in chimpanzees was investigated in the hope of ultimate application to interruption of vertical transmission. In previous experiments, no protection was observed when relatively high challenge doses were used. This study shows that HIVIG protected against a challenge dose (10 CID50) tenfold lower than that used previously. The protected animal remained free of HIV infection as determined by cocultivation and by polymerase chain reaction (PCR), and did not mount a primary immune response detectable by enzyme-linked immunosorbant assay (ELISA) and neutralization assays. These results imply that HIV vaccines should induce neutralizing antibody and may not need to induce cell-mediated immunity in order to be protective against exposure to HIV. They also provide an experimental basis for the conduct of clinical trials to evaluate prevention of maternal-infant transmission by HIVIG.
为了最终将其应用于阻断垂直传播,对使用人类免疫缺陷病毒(HIV)免疫球蛋白(HIVIG)预防黑猩猩感染HIV进行了研究。在先前的实验中,当使用相对较高的攻击剂量时未观察到保护作用。本研究表明,HIVIG可抵御比先前使用剂量低十倍的攻击剂量(10个半数感染剂量50 [CID50])。通过共培养和聚合酶链反应(PCR)确定,受保护的动物未感染HIV,并且通过酶联免疫吸附测定(ELISA)和中和试验未检测到初级免疫反应。这些结果表明,HIV疫苗应诱导中和抗体,并且可能无需诱导细胞介导的免疫即可预防HIV暴露。它们还为开展临床试验以评估HIVIG预防母婴传播提供了实验依据。