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新西兰白兔中的兔痘:根据 FDA 动物规则评估痘病毒医疗对策的治疗模型。

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

机构信息

Battelle, Biomedical Research Center, West Jefferson, OH, United States.

U.S. Department of Health and Human Services, Biomedical Advanced Research and Development Authority, Washington, DC, United States.

出版信息

Front Cell Infect Microbiol. 2018 Oct 5;8:356. doi: 10.3389/fcimb.2018.00356. eCollection 2018.

Abstract

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 LD < 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.

摘要

作为一种地方性疾病,天花已被根除,而且临床挑战也明显存在伦理问题,因此需要使用 FDA 的动物规则来评估针对天花的医疗对策的疗效。这种方法需要在一种动物模型中评估抗病毒疗效,该模型的感染足以充分重现人类疾病,从而提供对策有效性的预测价值。天花病毒的宿主范围狭窄,这意味着没有其他动物物种对天花病毒足够敏感,无法表现出具有预测价值的疾病。为了解决这个难题,在 2011 年 12 月与病毒学家进行了公开论坛后,FDA 建议开发两种感染同源正痘病毒的动物模型,即兔皮内感染和小鼠鼻腔内感染,以补充使用中的非人类灵长类动物模型。在本文中,我们描述了用兔痘病毒(RPXV)建立新西兰白兔皮内挑战模型用于痘病毒对策评估的方法。在 9 周和 16 周龄的兔子中,RPXV 的致死性 LD < 10 PFU。在致死性挑战 300 PFU 时,通过监测临床数据中异常值出现的时间,记录了两个年龄段兔子中 RPXV 感染的自然史。所有感染的动物都出现病毒血症、发热、体重减轻、出现继发性病变,并在 7 或 8 天后安乐死。16 周龄的 RPXV 感染动物的临床症状与 9 周龄兔子相似,但安乐死时间晚一天左右。对于所有动物,感染的两个最早的明确指标分别是通过定量聚合酶链反应检测到病毒拷贝数和在挑战后 2 天和 3 天出现发热。这些生物标志物为启动治疗提供了临床相关的触发因素。使用 16 周龄 NZW 兔子的主要优势是,较老的兔子更健壮,较少受到应激诱导的死亡影响,从而使研究更具可重复性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1b1/6182097/c22e2b127986/fcimb-08-00356-g0001.jpg

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