首页> 美国卫生研究院文献>Frontiers in Cellular and Infection Microbiology >Rabbitpox in New Zealand White Rabbits: A Therapeutic Model for Evaluation of Poxvirus Medical Countermeasures Under the FDA Animal Rule
【2h】

Rabbitpox in New Zealand White Rabbits: A Therapeutic Model for Evaluation of Poxvirus Medical Countermeasures Under the FDA Animal Rule

机译:新西兰白兔中的兔痘:根据FDA动物法规评估痘病毒医学对策的治疗模型

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。

摘要

The elimination of smallpox as an endemic disease and the obvious ethical problems with clinical challenge requires the efficacy evaluation of medical countermeasures against smallpox using the FDA Animal Rule. This approach requires the evaluation of antiviral efficacy in an animal model whose infection recapitulates the human disease sufficiently well enough to provide predictive value of countermeasure effectiveness. The narrow host range of variola virus meant that no other animal species was sufficiently susceptible to variola to manifest a disease with predictive value. To address this dilemma, the FDA, after a public forum with virologists in December 2011, suggested the development of two animal models infected with the cognate orthopoxvirus, intradermal infection of rabbits and intranasal infection of mice, to supplement the non-human primate models in use. In this manuscript, we describe the development of an intradermal challenge model of New Zealand White rabbits with rabbitpox virus (RPXV) for poxvirus countermeasure evaluation. Lethality of RPXV was demonstrated in both 9 and 16-weeks old rabbits with an LD50 < 10 PFU. The natural history of RPXV infection was documented in both ages of rabbits by monitoring the time to onset of abnormal values in clinical data at a lethal challenge of 300 PFU. All infected animals became viremic, developed a fever, exhibited weight loss, developed secondary lesions, and were euthanized after 7 or 8 days. The 16-weeks RPXV-infected animals exhibiting similar clinical signs with euthanasia applied about a day later than for 9-weeks old rabbits. For all animals, the first two unambiguous indicators of infection were detection of viral copies by quantitative polymerase chain reaction and fever at 2 and 3 days following challenge, respectively. These biomarkers provide clinically-relevant trigger(s) for initiating therapy. The major advantage for using 16-weeks NZW rabbits is that older rabbits were more robust and less subject to stress-induced death allowing more reproducible studies.
机译:消除天花作为地方病和具有临床挑战的明显伦理问题,需要使用FDA动物法则对针对天花的医学对策进行功效评估。这种方法需要在动物模型中评估抗病毒功效,该动物模型的感染足以很好地概括人类疾病,以提供对策有效性的预测价值。天花病毒的寄主范围很窄,这意味着没有其他动物物种足以感染天花,从而无法显示具有预测价值的疾病。为了解决这一难题,FDA在2011年12月与病毒学家举行了一次公开论坛后,建议开发两种感染了同源正痘病毒的动物模型,兔子的皮内感染和小鼠的鼻内感染,以补充非人类的灵长类动物模型。采用。在此手稿中,我们描述了新西兰白兔与兔痘病毒(RPXV)的皮内攻击模型的开发,用于痘病毒对策评估。在LD50 <10 PFU的9周和16周龄兔子中均证实了RPXV的致死性。在300 PFU的致死性攻击下,通过监测临床数据中异常值出现的时间来记录RPXV感染的自然史(在两个年龄的兔子中)。所有感染的动物变为病毒血症,发烧,体重减轻,继发性病变,并在7或8天后安乐死。与9周龄的兔子相比,约16天被RPXV感染的动物表现出相似的临床症状,但安乐死的时间大约晚一天。对于所有动物,感染的前两个明确指标是分别通过定量聚合酶链反应和攻击后第2天和第3天发烧检测病毒拷贝。这些生物标记物为临床治疗提供了临床相关的触发因素。使用16周NZW兔的主要优点是,年长的兔子更健壮,受应激诱导的死亡的可能性更低,从而可以进行更多可重复的研究。

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