Li A, Katinger H, Posner M R, Cavacini L, Zolla-Pazner S, Gorny M K, Sodroski J, Chou T C, Baba T W, Ruprecht R M
Laboratory of Viral Pathogenesis, Dana-Farber Cancer Institute, and Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 1998 Apr;72(4):3235-40. doi: 10.1128/JVI.72.4.3235-3240.1998.
We have tested triple and quadruple combinations of human monoclonal antibodies (MAbs), which are directed against various epitopes on human immunodeficiency virus type 1 (HIV-1) envelope glycoproteins, and a high-titer anti-HIV-1 human immunoglobulin (HIVIG) preparation for their abilities to neutralize a chimeric simian-human immunodeficiency virus (SHIV-vpu+). This virus encodes the HIV-1 strain IIIB env, tat, rev, and vpu genes. The quantitative nature of the Chou-Talalay method (Adv. Enzyme Regul. 22:27-55, 1984) allows ranking of various combinations under identical experimental conditions. Of all triple combinations tested, the most potent neutralization was seen with MAbs 694/98D plus 2F5 plus 2G12 (directed against domains on V3, gp41, and gp120, respectively) as measured by the total MAb concentration required to reach 90% neutralization (90% effective concentration [EC90], 2.0 microg/ml). All triple combinations involving MAbs and/or HIVIG that were tested yielded synergy with combination index values of < 1; the dose reduction indices (DRIs) ranged from 3.1 to 26.2 at 90% neutralization. When four MAbs (the previous three plus MAb F105, directed against the CD4 binding site) were combined, higher neutralization potency (EC90 1.8 microg/ml) and a higher degree of synergy compared to any triple combination were seen. The mean DRIs of the quadruple combination were approximately twice that of the most synergistic triple combination. We conclude that human MAbs targeting different HIV-1 envelope glycoprotein epitopes exhibit strong synergy when used in combination, a fact that could be exploited clinically for passive immunoprophylaxis against HIV-1.
我们测试了针对人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白上不同表位的人源单克隆抗体(MAb)的三联和四联组合,以及一种高滴度抗HIV-1人免疫球蛋白(HIVIG)制剂对嵌合型猴-人免疫缺陷病毒(SHIV-vpu+)的中和能力。该病毒编码HIV-1 IIIB株的env、tat、rev和vpu基因。Chou-Talalay方法(《酶调节进展》22:27-55,1984)的定量特性使得在相同实验条件下能够对各种组合进行排名。在所测试的所有三联组合中,最有效的中和作用是由MAb 694/98D加2F5加2G12(分别针对V3、gp41和gp120上的结构域)实现的,通过达到90%中和所需的总MAb浓度(90%有效浓度[EC90],2.0微克/毫升)来衡量。所有测试的涉及MAb和/或HIVIG的三联组合均产生协同作用,组合指数值<1;在90%中和时剂量降低指数(DRI)范围为3.1至26.2。当四种MAb(前三种加针对CD4结合位点的MAb F105)组合时,与任何三联组合相比,观察到更高的中和效力(EC90 1.8微克/毫升)和更高程度的协同作用。四联组合的平均DRI约为最具协同作用的三联组合的两倍。我们得出结论,靶向不同HIV-1包膜糖蛋白表位的人源MAb联合使用时表现出强大的协同作用这一事实可在临床上用于被动免疫预防HIV-1。