Montefiori D C, Graham B S, Kliks S, Wright P F
Department of Pathology, Vanderbilt University Medical School, Nashville, Tennessee 37232.
J Clin Immunol. 1992 Nov;12(6):429-39. doi: 10.1007/BF00918855.
Serum antibody responses were studied in detail in four vaccinia-naive volunteers in a phase I trial evaluating primary vaccination with a recombinant vaccinia virus expressing the HIV-1 gp160 envelope glycoprotein (HIVAC-1e, Oncogen/Bristol-Myers Squibb), followed by booster immunization with baculovirus-derived rgp160 (VaxSyn, MicroGeneSys). Prior to boosting, low-titer Fc receptor (FcR)-mediated, antibody-dependent enhancing (ADE) activity was detected in two of four volunteers but no IgM, IgG, IgA, neutralizing activity, or complement-mediated ADE activity was detected. Two weeks after boosting, all four volunteers developed HIV-1-specific IgG with titers of 1:160 to 1:640 by immunofluorescence assay. IgG1 was present in sera from each individual, while IgG2 and IgG3 were present in sera from two individuals, and IgG4 was present in serum from one individual. IgM and IgA were undetectable in all sera. Only one volunteer had IgG to the heterologous HIV-1 isolates, RF, MN, and SF2, after boosting. Serum from this volunteer neutralized the vaccine strain, LAV/IIIB, but not the heterologous strains, RF, MN, and SF2. Antibodies from the remaining volunteers had no neutralizing activity. The neutralizing serum had a positive reaction in a peptide-based ELISA utilizing a peptide corresponding to the principal neutralizing domain of the third hypervariable region (i.e., V3 loop) of the envelope glycoprotein. Neutralizing activity was partially removed by adsorption to this peptide, suggesting that it contained a type-specific neutralizing vaccine epitope. A low titer (1:40 to 1:80) of complement-mediated ADE activity to HIV-1 IIIB was present in sera from three vaccinees after boosting. FcR-ADE activity for HIV-1 SF2 and SF-128A were present in sera from two of these three vaccinees. None of the volunteers developed antisyncytial antibodies. These results indicate that inoculation with recombinant vaccinia followed by rgp160 boosting is the most effective strategy to date for inducing serum antibodies to the envelope glycoproteins of HIV-1, but further study is needed to optimize the functionality and cross-reactivity of these responses.
在一项I期试验中,对4名未接种过牛痘的志愿者的血清抗体反应进行了详细研究。该试验评估了用表达HIV-1 gp160包膜糖蛋白的重组牛痘病毒(HIVAC-1e,Oncogen/百时美施贵宝公司)进行初次接种,随后用杆状病毒衍生的rgp160(VaxSyn,MicroGeneSys公司)进行加强免疫。在加强免疫前,4名志愿者中有2名检测到低滴度的Fc受体(FcR)介导的抗体依赖性增强(ADE)活性,但未检测到IgM、IgG、IgA、中和活性或补体介导的ADE活性。加强免疫两周后,所有4名志愿者通过免疫荧光测定法产生了HIV-1特异性IgG,滴度为1:160至1:640。每个个体的血清中均存在IgG1,两名个体的血清中存在IgG2和IgG3,一名个体的血清中存在IgG4。所有血清中均未检测到IgM和IgA。加强免疫后,只有一名志愿者对异源HIV-1分离株RF、MN和SF2产生了IgG。该志愿者的血清中和了疫苗株LAV/IIIB,但未中和异源株RF、MN和SF2。其余志愿者的抗体无中和活性。在基于肽的ELISA中,中和血清利用与包膜糖蛋白第三个高变区(即V3环)主要中和结构域对应的肽产生了阳性反应。通过吸附到该肽上,中和活性部分被去除,表明其含有一种型特异性中和疫苗表位。加强免疫后,三名接种疫苗者的血清中存在低滴度(1:40至1:80)的针对HIV-1 IIIB的补体介导的ADE活性。这三名接种疫苗者中有两名的血清中存在针对HIV-1 SF2和SF-128A的FcR-ADE活性。所有志愿者均未产生抗合胞体抗体。这些结果表明,接种重组牛痘病毒后再用rgp160加强免疫是迄今为止诱导针对HIV-1包膜糖蛋白血清抗体的最有效策略,但需要进一步研究以优化这些反应的功能和交叉反应性。