Tefit Josianne Nitcheu, Crabé Sandrine, Orlandini Bernard, Nell Haylene, Bendelac Albert, Deng Shenglou, Savage Paul B, Teyton Luc, Serra Vincent
Abivax, 5 rue Henri Desbruères, 91030 Evry cedex, France.
Phinc, 5, rue Henri Desbruères Immeuble Genavenir 8 91030 Evry, France.
Vaccine. 2014 Oct 21;32(46):6138-45. doi: 10.1016/j.vaccine.2014.08.070. Epub 2014 Sep 13.
We have assessed the immune-regulatory and adjuvant activities of a synthetic glycolipid, ABX196, a novel analog of the parental compound α-GalCer. As expected, ABX196 demonstrated a measurable and significant adjuvant effect in mice and monkeys with no appreciable toxicity at the doses used to promote immune responses. We performed a phase I/II dose escalation study of ABX196 in healthy volunteers, with the objectives to evaluate its safety profile, as well as its ability to be utilized as an adjuvant in the context of a prophylactic vaccine against hepatitis B. ABX196 was administered at three doses: 0.2, 0.4, and 2.0μg, in 44 subjects. In all the individuals injected with ABX196, peripheral blood NKT cells displayed hallmarks of activation, and 45% of them had measurable circulating IFN-γ 24h after the first administration. More importantly, the addition of ABX196 to the very poorly immunogenic HBs antigen resulted in protective anti-HBs antibody responses in majority of patients, demonstrating the adjuvant properties of ABX196 in human. Further analysis of the cohort of subjects receiving ABX196 with HBs antigen also indicates that a single injection appears sufficient to provide protection. A limited set of adverse events linked to the systemic delivery of ABX196 and access to the liver, is discussed in the context of formulation and the need to limit transport of ABX196 to secondary lymphoid tissues for maximal efficacy (Eudra-CT 2012-001566-15).
我们评估了一种合成糖脂ABX196的免疫调节和佐剂活性,它是母体化合物α-GalCer的新型类似物。正如预期的那样,ABX196在小鼠和猴子中显示出可测量的显著佐剂效应,在用于促进免疫反应的剂量下没有明显毒性。我们在健康志愿者中进行了ABX196的I/II期剂量递增研究,目的是评估其安全性,以及在乙型肝炎预防性疫苗中用作佐剂的能力。44名受试者接受了三种剂量的ABX196:0.2、0.4和2.0μg。在所有注射ABX196的个体中,外周血NKT细胞表现出活化特征,其中45%在首次给药后24小时有可测量的循环IFN-γ。更重要的是,将ABX196添加到免疫原性很差的HBs抗原中,在大多数患者中产生了保护性抗-HBs抗体反应,证明了ABX196在人体中的佐剂特性。对接受ABX196和HBs抗原的受试者队列的进一步分析还表明,单次注射似乎足以提供保护。在制剂的背景下讨论了与ABX196全身给药和进入肝脏相关的一组有限的不良事件,以及为了获得最大疗效而将ABX196转运限制到二级淋巴组织的必要性(欧盟临床试验注册号2012-001566-15)。