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豚鼠变应原诱导的迟发性哮喘反应中的T淋巴细胞和嗜酸性粒细胞

T lymphocytes and eosinophils in allergen-induced late-phase asthmatic reactions in the guinea pig.

作者信息

Frew A J, Moqbel R, Azzawi M, Hartnell A, Barkans J, Jeffery P K, Kay A B, Scheper R J, Varley J, Church M K

机构信息

Department of Allergy and Clinical Immunology, National Heart and Lung Institute, Brompton Hospital, London, U.K.

出版信息

Am Rev Respir Dis. 1990 Feb;141(2):407-13. doi: 10.1164/ajrccm/141.2.407.

DOI:10.1164/ajrccm/141.2.407
PMID:2137315
Abstract

The kinetics and phenotype of T lymphocytes infiltrating the airways of guinea pigs undergoing late-phase asthmatic reactions (LAR) were studied with monoclonal antibodies, cytofluorimetry, and immunocytochemistry. Challenge of sensitized animals with aerosolized ovalbumin was followed by early (2 h) and late-phase (17 h) bronchoconstriction. The induction of hypersensitivity, by aerosolized antigen, was associated with an increase in mucosal T cell numbers, which consisted almost entirely of CD8+ T cells. Following allergen challenge of fully sensitized animals, a biphasic rise in total T cell (CD3+) numbers was observed in the bronchial mucosa, peaking at 17 and 48 h. A similar pattern of T cell accumulation was observed in the bronchial adventitia but with an extra early peak at 2 h. In contrast to the T cell influx of the sensitization phase, the postchallenge infiltrate consisted largely of CD3+, CD8- cells. Eosinophil numbers were elevated in both submucosa and adventitia, with a single broad peak between 17 and 48 h. T cell infiltration was compared with eosinophil accumulation; while correlations between T cell and eosinophil numbers varied over the 96 h of the experiment, strong associations were observed between CD8+ numbers and eosinophils in the adventitia at 6 h (r = 0.733, p less than 0.01) and between CD3+ numbers and eosinophils in the submucosa at 72 h (r = 0.88, p less than 0.001). No significant changes were detected in T cell or eosinophil numbers in the lung parenchyma. There was a postchallenge increase in eosinophils (but not T cells) in bronchoalveolar lavage (BAL).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用单克隆抗体、细胞荧光测定法和免疫细胞化学方法,研究了豚鼠在迟发性哮喘反应(LAR)过程中浸润气道的T淋巴细胞的动力学和表型。用雾化卵清蛋白激发致敏动物后,出现早期(2小时)和迟发性(17小时)支气管收缩。雾化抗原诱导的超敏反应与黏膜T细胞数量增加有关,这些T细胞几乎全部由CD8+ T细胞组成。对完全致敏的动物进行过敏原激发后,在支气管黏膜中观察到总T细胞(CD3+)数量呈双相上升,在17小时和48小时达到峰值。在支气管外膜中观察到类似的T细胞聚集模式,但在2小时有一个额外的早期峰值。与致敏阶段的T细胞流入不同,激发后的浸润细胞主要由CD3+、CD8-细胞组成。黏膜下层和外膜中的嗜酸性粒细胞数量均升高,在17小时至48小时之间有一个单一的宽峰。将T细胞浸润与嗜酸性粒细胞聚集进行比较;虽然在实验的96小时内T细胞和嗜酸性粒细胞数量之间的相关性有所变化,但在6小时时外膜中CD8+细胞数量与嗜酸性粒细胞之间(r = 0.733,p < 0.01)以及在72小时时黏膜下层中CD3+细胞数量与嗜酸性粒细胞之间(r = 0.88,p < 0.001)观察到强相关性。肺实质中的T细胞或嗜酸性粒细胞数量未检测到显著变化。支气管肺泡灌洗(BAL)中激发后嗜酸性粒细胞(而非T细胞)数量增加。(摘要截断于250字)

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