Smee D F, Sugiyama S T, Sidwell R W, Barnett B B
Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan 84322-5600, USA.
Chemotherapy. 1995 Mar-Apr;41(2):141-8. doi: 10.1159/000239335.
The effects of monoclonal antibody used in combination with ganciclovir (GCV) or (S)-1-[3-hydroxy-(2-phosphonylmethoxy)propyl]cytosine (HPMPC) against murine cytomegalovirus (MCMV) were determined in vitro and in vivo, in mice. The antibody and drug were added to cell cultures 24 h after MCMV adsorption so as not to affect the initial infection rate. The antibody (at 1.25-20 micrograms/ml) combined with GCV (0.3-5 microM) or HPMPC (0.008-0.125 microM) caused synergistic inhibition of virus yield in C127I cells. No toxic effect on cell growth in culture was observed at these antibody/drug combinations. The effects of antibody and GCV treatments were studied in MCMV-infected severe combined immunodeficient (SCID) mice. Antibody treatments (2.5 mg/kg/day) given by intraperitoneal injection every 3 days starting 24 h after virus inoculation extended survival time by 1 day relative to placebo-treated animals. Once daily, intraperitoneal treatments with GCV (25 and 50 mg/kg/day) for 7 days starting at 24 h after virus inoculation extended survival time 9-11 days. The combination of antibody plus GCV was only slightly better than GCV alone, indicating an additive interaction.
在小鼠体内外研究了单克隆抗体与更昔洛韦(GCV)或(S)-1-[3-羟基-(2-膦酰甲氧基)丙基]胞嘧啶(HPMPC)联合使用对鼠巨细胞病毒(MCMV)的作用。在MCMV吸附24小时后将抗体和药物添加到细胞培养物中,以免影响初始感染率。抗体(1.25 - 20微克/毫升)与GCV(0.3 - 5微摩尔)或HPMPC(0.008 - 0.125微摩尔)联合使用可协同抑制C127I细胞中的病毒产量。在这些抗体/药物组合下未观察到对培养细胞生长的毒性作用。在感染MCMV的严重联合免疫缺陷(SCID)小鼠中研究了抗体和GCV治疗的效果。从病毒接种后24小时开始,每3天腹腔注射一次抗体治疗(2.5毫克/千克/天),相对于安慰剂治疗的动物,存活时间延长了1天。从病毒接种后24小时开始,每天一次腹腔注射GCV(25和50毫克/千克/天),持续7天,存活时间延长了9 - 11天。抗体加GCV的组合仅比单独使用GCV稍好,表明存在相加作用。