Laboratory of Adjuvant and Antigen Research, U.S. Military HIV Research Program, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, Maryland 20910, United States.
U.S. Military HIV Research Program, Henry M. Jackson Foundation for the Advancement of Military Medicine, 6720A Rockledge Drive, Bethesda, Maryland 20817, United States.
Mol Pharm. 2020 Sep 8;17(9):3447-3460. doi: 10.1021/acs.molpharmaceut.0c00497. Epub 2020 Aug 13.
Active immunization is an emerging potential modality to combat fatal overdose amid the opioid epidemic. In this study, we described the design, synthesis, formulation, and animal testing of an efficacious vaccine against fentanyl. The vaccine formulation is composed of a novel fentanyl hapten conjugated to tetanus toxoid (TT) and adjuvanted with liposomes containing monophosphoryl lipid A adsorbed on aluminum hydroxide. The linker and hapten -phenyl--(1-(4-(3-(tritylthio)propanamido)phenethyl)piperidin-4-yl)propionamide were conjugated sequentially to TT using amine--hydroxysuccinimide-ester and thiol-maleimide reaction chemistries, respectively. Conjugation was facile, efficient, and reproducible with a protein recovery of >98% and a hapten density of 30-35 per carrier protein molecule. In mice, immunization induced high and robust antibody endpoint titers in the order of >10 against the hapten. The antisera bound fentanyl, carfentanil, cyclopropyl fentanyl, -fluorofentanyl, and furanyl fentanyl with antibody-drug dissociation constants in the range of 0.36-4.66 nM. No cross-reactivity to naloxone, naltrexone, methadone, or buprenorphine was observed. , immunization shifted the antinociceptive dose-response curve of fentanyl to higher doses. Collectively, these preclinical results showcased the desired traits of a potential vaccine against fentanyl and demonstrated the feasibility of immunization to combat fentanyl-induced effects.
主动免疫是应对阿片类药物流行中致命过量的一种新兴潜在手段。在这项研究中,我们描述了一种针对芬太尼的有效疫苗的设计、合成、配方和动物试验。疫苗配方由一种新型芬太尼半抗原与破伤风类毒素(TT)偶联而成,并与含有吸附在氢氧化铝上的单磷酰脂质 A 的脂质体佐剂混合。连接子和半抗原 - 苯 - [1-(4-(3-(三苯甲基硫代)丙酰胺基)苯乙基)哌啶-4-基]丙酰胺分别通过胺 - 羟基琥珀酰亚胺酯和硫醇 - 马来酰亚胺反应化学与 TT 偶联。偶联是简便、高效和可重复的,蛋白回收率>98%,半抗原密度为每个载体蛋白分子 30-35 个。在小鼠中,免疫诱导了针对半抗原的高且强大的抗体效价终点,>10。抗血清结合芬太尼、卡芬太尼、环丙基芬太尼、-氟芬太尼和呋喃芬太尼,抗体-药物解离常数在 0.36-4.66 nM 范围内。未观察到与纳洛酮、纳曲酮、美沙酮或丁丙诺啡的交叉反应。此外,免疫使芬太尼的镇痛剂量反应曲线向更高剂量转移。总的来说,这些临床前结果展示了一种针对芬太尼的潜在疫苗的理想特性,并证明了免疫对抗芬太尼诱导效应的可行性。