Radiation Countermeasures Program, Scientific Research Department, Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
PLoS One. 2011;6(9):e25210. doi: 10.1371/journal.pone.0025210. Epub 2011 Sep 28.
The animal efficacy rule addressing development of drugs for selected disease categories has pointed out the need to develop alternative large animal models. Based on this rule, the pathophysiology of the disease in the animal model must be well characterized and must reflect that in humans. So far, manifestations of the acute radiation syndrome (ARS) have been extensively studied only in two large animal models, the non-human primate (NHP) and the canine. We are evaluating the suitability of the minipig as an additional large animal model for development of radiation countermeasures. We have previously shown that the Gottingen minipig manifests hematopoietic ARS phases and symptoms similar to those observed in canines, NHPs, and humans.
We establish here the LD50/30 dose (radiation dose at which 50% of the animals succumb within 30 days), and show that at this dose the time of nadir and the duration of cytopenia resemble those observed for NHP and canines, and mimic closely the kinetics of blood cell depletion and recovery in human patients with reversible hematopoietic damage (H3 category, METREPOL approach). No signs of GI damage in terms of diarrhea or shortening of villi were observed at doses up to 1.9 Gy. Platelet counts at days 10 and 14, number of days to reach critical platelet values, duration of thrombocytopenia, neutrophil stress response at 3 hours and count at 14 days, and CRP-to-platelet ratio were correlated with survival. The ratios between neutrophils, lymphocytes and platelets were significantly correlated with exposure to irradiation at different time intervals.
As a non-rodent animal model, the minipig offers a useful alternative to NHP and canines, with attractive features including ARS resembling human ARS, cost, and regulatory acceptability. Use of the minipig may allow accelerated development of radiation countermeasures.
针对选定疾病类别的药物开发的动物功效规则指出,需要开发替代的大型动物模型。基于这一规则,动物模型中的疾病病理生理学必须得到很好的描述,并且必须反映人类的情况。到目前为止,急性辐射综合征(ARS)的表现仅在两种大型动物模型,非人类灵长类动物(NHP)和犬类中得到广泛研究。我们正在评估小型猪作为开发辐射对策的另一种大型动物模型的适用性。我们之前已经表明,哥廷根小型猪表现出类似于犬类、NHP 和人类观察到的造血 ARS 阶段和症状。
我们在这里确定了 LD50/30 剂量(辐射剂量,其中 50%的动物在 30 天内死亡),并表明在此剂量下,最低点时间和细胞减少症的持续时间与 NHP 和犬类观察到的相似,并且非常接近人类可逆造血损伤患者(H3 类,METREPOL 方法)中血细胞耗竭和恢复的动力学。在高达 1.9 Gy 的剂量下,没有观察到腹泻或绒毛缩短等胃肠道损伤的迹象。在第 10 天和第 14 天的血小板计数、达到临界血小板值的天数、血小板减少症的持续时间、3 小时的中性粒细胞应激反应和 14 天的计数以及 CRP 与血小板的比值与存活率相关。中性粒细胞、淋巴细胞和血小板之间的比值与不同时间间隔的照射暴露显著相关。
作为一种非啮齿类动物模型,小型猪为 NHP 和犬类提供了一种有用的替代方案,具有相似的人类 ARS、成本和监管可接受性等吸引人的特点。使用小型猪可能允许加速开发辐射对策。