首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >9-(1-3-Dihydroxy-2-propoxymethyl)guanine prevents death but not immunity in murine cytomegalovirus-infected normal and immunosuppressed BALB/c mice.
【2h】

9-(1-3-Dihydroxy-2-propoxymethyl)guanine prevents death but not immunity in murine cytomegalovirus-infected normal and immunosuppressed BALB/c mice.

机译:9-(1-3-二羟基-2-丙氧基甲基)鸟嘌呤可预防小鼠巨细胞病毒感染的正常和免疫抑制的BALB / c小鼠的死亡但不能阻止其免疫。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Immunosuppressed (from treatment with cortisone acetate and anti-thymocyte globulin) and control adult female BALB/c mice, latently infected with murine cytomegalovirus (MCMV) or lethally challenged (10(6) PFU) with MCMV intraperitoneally, were treated with 9-(1-3-dihydroxy-2-propoxymethyl)guanine (DHPG) intraperitoneally. A dose of 3 mg/kg reduced mortality by 50% in lethally challenged normal mice; 10 mg/kg was required in immunosuppressed mice. When 15 mg/kg was given, the onset of treatment could be delayed for 64 h after lethal challenge. DHPG did not prevent the establishment of latent MCMV infection or immunosuppression-induced reactivation. The antibody titer to MCMV in DHPG-treated mice which survived lethal challenge was 41 (reciprocal of geometric mean) 4 to 5 weeks after inoculation; such mice survived a second lethal challenge. When antiserum treatment was begun 64 h and DHPG was begun 72 h after a lethal challenge, most mice survived; most did not when either treatment alone was begun at those times. In summary, DHPG effectively treated lethal MCMV infection even in immunosuppressed mice and even when treatment onset was delayed for 64 h. Treatment did not alter the establishment or reactivation of latent infections or the induction of effective immunity. The administration of DHPG coupled with antiserum treatment may be even more effective than the administration of either alone.
机译:用9-(-腹膜内的1-3-二羟基-2-丙氧基甲基)鸟嘌呤(DHPG)。给予致命攻击的正常小鼠3 mg / kg的剂量可使死亡率降低50%;免疫抑制的小鼠需要10 mg / kg。当给予15 mg / kg的剂量时,致命攻击后可以将治疗开始延迟64小时。 DHPG不能阻止潜在MCMV感染的建立或免疫抑制诱导的再激活。在接受致死性攻击的DHPG处理小鼠中,MCMV抗体滴度在接种后4至5周为41(几何平均值的倒数);这样的小鼠在第二次致命的攻击中存活下来。致死攻击后64小时开始抗血清治疗,DHPG开始72小时后,大多数小鼠存活。在那时候开始单独使用任何一种疗法时,大多数都没有。总之,即使在免疫抑制的小鼠中,甚至在治疗开始延迟了64小时后,DHPG仍能有效治疗致命的MCMV感染。治疗没有改变潜伏感染的建立或重新激活或有效免疫的诱导。 DHPG的联合抗血清治疗可能比单独施用任何一种更为有效。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号