SNBL USA, Ltd, Everett, WA.
Northwest Medical Physics Center, Lynnwood, WA.
Health Phys. 2019 Mar;116(3):354-365. doi: 10.1097/HP.0000000000000925.
Radiation-induced lung injury is a characteristic, dose- and time-dependent sequela of potentially lethal, delayed effects of acute radiation exposure. Understanding of these delayed effects to include development of medical countermeasures requires well-characterized and validated animal models that mimic the human response to acute radiation and adhere to the criteria of the US Food and Drug Administration Animal Rule. The objective herein was to establish a nonhuman primate model of whole-thorax lung irradiation in female rhesus macaques. Definition of the dose-response relationship to include key signs of morbidity and mortality in the female macaque served to independently validate the recent model performed with male macaques and importantly, to establish the lack of sex and institutional bias across the dose-response relationship for radiation-induced lung injury. The study design was similar to that described previously, with the exception that female rhesus macaques were utilized. In brief, a computed tomography scan was conducted prior to irradiation and used for treatment planning. Animals in 5 cohorts (n = 8 per cohort) were exposed to a single 6-MV photon exposure focused on the lung as determined by the computed tomography scan and treatment planning at a dose of 9.5, 10, 10.5, 11, or 11.5 Gy. Subject-based supportive care, including administration of dexamethasone, was based on trigger-to-treat criteria. Clearly defined euthanasia criteria were used to determine a moribund condition over the 180-day study duration post-whole-thorax lung irradiation. Percent mortality per radiation dose was 12.5% at 9.5 Gy, 25% at 10 Gy, 62.5% at 10.5 Gy, 87.5% at 11 Gy, and 100% at 11.5 Gy. The resulting probit plot for the whole-thorax lung irradiation model estimated an LD50/180 of 10.28 Gy, which was not significantly different from the published estimate of 10.27 Gy for the male rhesus. The key parameters of morbidity and mortality support the conclusion that there is an absence of a sex influence on the radiation dose-response relationship for whole-thorax lung irradiation in the rhesus macaque. This work also provides a significant interlaboratory validation of the previously published model.
放射性肺损伤是一种具有特征性、剂量依赖性和时间依赖性的潜在致命性、急性辐射暴露后延迟效应。为了更好地了解这些延迟效应,包括开发医疗对策,需要使用经过良好特征描述和验证的动物模型,这些模型模拟人类对急性辐射的反应,并符合美国食品和药物管理局动物规则的标准。本研究的目的是建立一种雌性恒河猴全胸肺照射的非人类灵长类动物模型。定义剂量-反应关系,包括雌性猕猴发病和死亡的关键体征,这不仅独立验证了最近在雄性猕猴中进行的模型,而且重要的是,为放射性肺损伤的剂量-反应关系建立了缺乏性别和机构偏见的证据。该研究设计与之前描述的设计相似,只是使用了雌性恒河猴。简而言之,在照射前进行计算机断层扫描,并用于治疗计划。5 个队列(每个队列 8 只动物)的动物接受单次 6-MV 光子照射,照射部位为根据计算机断层扫描和治疗计划确定的肺部,剂量为 9.5、10、10.5、11 或 11.5 Gy。基于触发-治疗标准,对每只动物进行基于个体的支持性护理,包括地塞米松的给药。在整个 180 天的全胸肺照射研究期间,使用明确定义的安乐死标准来确定濒死状态。在 9.5 Gy 时,死亡率为 12.5%,在 10 Gy 时为 25%,在 10.5 Gy 时为 62.5%,在 11 Gy 时为 87.5%,在 11.5 Gy 时为 100%。全胸肺照射模型的概率单位绘图估计整个胸部肺照射的 LD50/180 为 10.28 Gy,与之前发表的雄性恒河猴 10.27 Gy 的估计值没有显著差异。发病率和死亡率的关键参数支持这样的结论,即全胸肺照射在雌性恒河猴中不存在性别对辐射剂量-反应关系的影响。这项工作还为之前发表的模型提供了重要的实验室间验证。