Stieneker F, Kreuter J, Löwer J
Institut für Pharmazeutische Technologie, Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
AIDS. 1991 Apr;5(4):431-5. doi: 10.1097/00002030-199104000-00012.
The aim of the present study was to determine the effect of polymethylmethacrylate (PMMA) nanoparticles as adjuvants for an HIV-2 whole-virus vaccine in mice. The data clearly revealed that PMMA nanoparticles induced 10-100-fold higher antibody titres than aluminium hydroxide or an aqueous vaccine control preparation as measured by enzyme-linked immunosorbent assay. Moreover, the high antibody titres obtained with PMMA as adjuvant appeared to be stable for between 10 and 20 weeks after immunization. In contrast, the titres of the control preparations, fluid or aluminium hydroxide formulations, decreased after 10 weeks.
本研究的目的是确定聚甲基丙烯酸甲酯(PMMA)纳米颗粒作为HIV-2全病毒疫苗佐剂对小鼠的影响。数据清楚地显示,通过酶联免疫吸附测定法测得,PMMA纳米颗粒诱导产生的抗体滴度比氢氧化铝或水性疫苗对照制剂高10至100倍。此外,以PMMA作为佐剂获得的高抗体滴度在免疫后10至20周内似乎保持稳定。相比之下,对照制剂(液体或氢氧化铝制剂)的滴度在10周后下降。