首页> 外文期刊>Annals of allergy, asthma, and immunology >Validation of the biogenics research chamber for Juniperus ashei (mountain cedar) pollen.
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Validation of the biogenics research chamber for Juniperus ashei (mountain cedar) pollen.

机译:杜松杜松花粉生物遗传学研究室的验证。

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BACKGROUND: Pollen challenge chambers have been used to evaluate medication in allergic rhinoconjunctivitis under controlled conditions. OBJECTIVE: To validate a facility for the study of subjects' responses to inhalational challenges with Juniperus ashei (mountain cedar) pollen. METHODS: Two chambers, 307 m(3) and 188 m(3), seating 50 and 25 individuals, respectively, were constructed with clean room materials. The computer-controlled air handler used powered diffusers and exhausts to maintain a laminar flow. Pollen was delivered by a feeder into a vortex created by an eductor through a series of stainless steel tubes. Nonprimed mountain cedar sensitive and healthy control subjects were exposed to a masked sham air run and increasing increments of pollen during a 5-hour period outside the natural season. These individuals were then exposed for 2-hour periods for up to 4 sequential days at fixed pollen counts to demonstrate effects of priming. RESULTS: Airflow from diffusers and exhausts maintained 12 exchange cycles per hour. Pollen counts ranged from 1,300 to 12,000 grains/m(3). None of the subjects responded during the masked sham run. Healthy controls did not respond. Nonprimed subjects had an inadequate response. Primed subjects responded symptomatically within a period adequate for entry into studies. There were no serious adverse responses. CONCLUSIONS: The chambers functioned within the parameters for which they were designed. Subjects did not respond to a sham run. Priming runs were required to stimulate symptoms at levels in a timeframe sufficient for pharmacologic studies. Pollen counts 3 to 4 times the average seasonal counts were required to elicit significant symptoms.
机译:背景:花粉激发室已用于评估在受控条件下过敏性鼻结膜炎中的药物。目的:验证用于研究受试者对山茱Jun(Juniperus ashei)(山杉)花粉的吸入挑战反应的设施。方法:两个房间分别为307 m(3)和188 m(3),分别容纳50和25个人,使用洁净室材料建造。由计算机控制的空气处理器使用动力扩散器和排气口来保持层流。花粉由进料器通过一系列不锈钢管送入由喷射器产生的涡流中。在自然季节以外的5个小时内,未经初免刺激的雪松和健康对照者要接受假面伪装空气传播,并增加花粉增量。然后将这些个体以固定的花粉计数暴露2小时,最多连续4天,以证明引发效应。结果:扩散器和排气的气流每小时保持12个交换周期。花粉计数范围为1300至12,000粒/ m(3)。在伪装假面跑步期间,没有受试者反应。健康对照者无反应。非初级受试者的反应不足。预备受试者在足以进入研究阶段的时间内对症反应。没有严重的不良反应。结论:室的功能在其设计的参数范围内。受试者对假手术没有反应。需要进行启动试验以在足以进行药理学研究的时间范围内刺激症状。花粉计数为引起明显症状所需的平均季节性计数的3至4倍。

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