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恒河猴急性放射综合征的造血综合征:致死剂量反应关系的系统评价

The Hematopoietic Syndrome of the Acute Radiation Syndrome in Rhesus Macaques: A Systematic Review of the Lethal Dose Response Relationship.

作者信息

MacVittie Thomas J, Farese Ann M, Jackson William

机构信息

*University of Maryland, School of Medicine, Baltimore, MD; †Statistician, Rockville, MD.

出版信息

Health Phys. 2015 Nov;109(5):342-66. doi: 10.1097/HP.0000000000000352.

Abstract

Well characterized animal models that mimic the human response to potentially lethal doses of radiation are required to assess the efficacy of medical countermeasures under the criteria of the U.S. Food and Drug Administration "animal rule." Development of a model requires the determination of the radiation dose response relationship and time course of mortality and morbidity across the hematopoietic acute radiation syndrome. The nonhuman primate, rhesus macaque, is a relevant animal model that may be used to determine the efficacy of medical countermeasures to mitigate major signs of morbidity and mortality at selected lethal doses of total body irradiation. A systematic review of relevant studies that determined the dose response relationship for the hematopoietic acute radiation syndrome in the rhesus macaque relative to radiation quality, dose rate, and exposure uniformity has never been performed. The selection of data cohorts was made from the following sources: Ovid Medline (1957-present), PubMed (1954-present), AGRICOLA (1976-present), Web of Science (1954-present), and U.S. HHS REPORT (2002 to present). The following terms were used: Rhesus, total body-irradiation, total body x irradiation, TBI, irradiation, gamma radiation, hematopoiesis, LD50/60, Macaca mulatta, whole-body irradiation, nonhuman primate, NHP, monkey, primates, hematopoietic radiation syndrome, mortality, and nuclear radiation. The reference lists of all studies, published and unpublished, were reviewed for additional studies. The total number of hits across all search sites was 3,001. There were a number of referenced, unpublished, non-peer reviewed government reports that were unavailable for review. Fifteen studies, 11 primary (n = 863) and four secondary (n = 153) studies [n = 1,016 total nonhuman primates (NHP), rhesus Macaca mulatta] were evaluated to provide an informative and consistent review. The dose response relationships (DRRs) were determined for uniform or non-uniform total body irradiation (TBI) with 250 kVp or 2 MeV x radiation, Co gamma radiation and reactor- and nuclear weapon-derived mixed gamma: neutron-radiation, delivered at various dose rates from a total body, bilateral, rotational, or unilateral exposure aspect. The DRRs established by a probit analysis vs. linear dose relationship were characterized by two main parameters or dependent variables: a slope and LD50/30. Respective LD50/30 values for studies that used 250 kVp x radiation (five primary studies combined, n = 338), 2 MeV x radiation, Co gamma radiation, and steady-state reactor-derived mixed gamma:neutron radiation for total body uniform exposures were 521 rad [498, 542], 671 rad [632, 715], 644 rad [613, 678], and 385 rad [357, 413]. The respective slopes were steep and ranged from 0.738 to 1.316. The DRR, LD50/30 values and slopes were also determined for total body, non-uniform, unilateral, pulse-rate exposures of mixed gamma:neutron radiation derived at reactor and nuclear weapon detonations. The LD50/30 values were, respectively, 395 rad [337, 432] and 412 rad [359, 460]. Secondary data sets of limited studies that did not describe a DRR were used to support the mid-to-high lethal dose range for the H-ARS and the threshold dose range for the concurrent acute GI ARS. The available evidence provided a reliable and extensive database that characterized the DRR for the H-ARS in young rhesus macaques exposed to 250 kVp uniform total body x radiation without the benefit of medical management. A less substantial but consistent database demonstrated the DRR for total body exposure of differing radiation quality, dose rate and non-uniform exposure. The DRR for the H-ARS is characterized by steep slopes and relative LD50/30 values that reflect the radiation quality, exposure aspect, and dose rate over a range in time from 1954-2012.

摘要

为了根据美国食品药品监督管理局的“动物规则”标准评估医学应对措施的疗效,需要有特征明确的动物模型来模拟人类对潜在致死剂量辐射的反应。建立一个模型需要确定造血急性放射综合征的辐射剂量反应关系以及死亡率和发病率随时间的变化过程。非人灵长类动物恒河猴是一种相关的动物模型,可用于确定医学应对措施在选定的全身照射致死剂量下减轻发病和死亡主要体征的疗效。从未对相关研究进行过系统综述,这些研究确定了恒河猴造血急性放射综合征相对于辐射质量、剂量率和照射均匀性的剂量反应关系。数据队列的选择来自以下来源:Ovid Medline(1957年至今)、PubMed(1954年至今)、AGRICOLA(1976年至今)、Web of Science(1954年至今)和美国卫生与公众服务部报告(2002年至今)。使用了以下术语:恒河猴、全身照射、全身X射线照射、TBI、照射、γ辐射、造血、LD50/60、猕猴、全身照射、非人灵长类动物、NHP、猴子、灵长类动物、造血放射综合征、死亡率和核辐射。对所有已发表和未发表研究的参考文献列表进行了审查,以查找其他研究。所有搜索站点的命中总数为3001条。有许多引用的、未发表的、未经同行评审的政府报告无法进行审查。对15项研究进行了评估,其中11项为主要研究(n = 863),4项为次要研究(n = 153)[总共1016只非人灵长类动物(NHP),恒河猴猕猴],以提供内容丰富且一致的综述。确定了用250 kVp或2 MeV X射线、钴γ辐射以及反应堆和核武器产生的混合γ:中子辐射进行均匀或非均匀全身照射(TBI)的剂量反应关系(DRR),这些辐射以不同的剂量率从全身、双侧、旋转或单侧照射角度进行照射。通过概率分析与线性剂量关系建立的DRR由两个主要参数或因变量表征:斜率和LD50/30。对于使用250 kVp X射线(五项主要研究合并,n = 338)、2 MeV X射线、钴γ辐射以及稳态反应堆产生的混合γ:中子辐射进行全身均匀照射的研究,各自的LD50/30值分别为521 rad [498, 542]、671 rad [632, 715]、644 rad [613, 678]和385 rad [357, 413]。各自的斜率较陡,范围为0.738至1.316。还确定了反应堆和核武器爆炸产生的混合γ:中子辐射的全身、非均匀、单侧、脉冲率照射的DRR、LD50/30值和斜率。LD50/30值分别为395 rad [337, 432]和412 rad [359, 460]。未描述DRR的有限研究的次要数据集用于支持造血急性放射综合征的中高致死剂量范围以及并发急性胃肠道放射综合征的阈值剂量范围。现有证据提供了一个可靠且广泛的数据库,该数据库表征了在未接受医学处理的情况下,暴露于250 kVp均匀全身X射线下的年轻恒河猴造血急性放射综合征的DRR。一个规模较小但一致的数据库展示了不同辐射质量、剂量率和非均匀照射的全身照射的DRR。造血急性放射综合征的DRR的特征是斜率较陡以及相对LD50/30值,这些值反映了1954年至2012年期间不同时间范围内的辐射质量、照射角度和剂量率。

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