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变应原诱导哮喘患者骨髓T淋巴细胞增加及白细胞介素-5表达升高。

Allergen-induced increases in bone marrow T lymphocytes and interleukin-5 expression in subjects with asthma.

作者信息

Wood Lorna J, Sehmi Roma, Dorman Sandra, Hamid Qutayba, Tulic Meri K, Watson Richard M, Foley Ronan, Wasi Parveen, Denburg Judah A, Gauvreau Gail, O'Byrne Paul M

机构信息

Asthma Research Group, Firestone Institute for Respiratory Health, St. Joseph's Hospital and the Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Am J Respir Crit Care Med. 2002 Sep 15;166(6):883-9. doi: 10.1164/rccm.2108015.

Abstract

Inhaled allergen challenge of subjects with atopic asthmatic increases bone marrow eosinophil progenitor cells. Interleukin-5 (IL-5) specifically induces growth and maturation of eosinophils. This study examined the effect of allergen challenge on the number of bone marrow total and CD3+ cells expressing IL-5 protein and IL-5 mRNA in subjects with asthma who developed either allergen-induced isolated early responses, or early and late asthmatic responses (dual responders). At 24 hours after allergen challenge, dual responders had significantly greater blood and airway eosinophilia compared with early responders. There were significant increases in the percentage of bone marrow CD3+ cells (p < 0.005) in both groups. However, there were significant differences in the increases in bone marrow IL-5 mRNA+ (p < 0.005), CD3+ (p < 0.005), and IL-5 mRNA+ CD3+ (p < 0.005) cells between the dual and early responder groups. These results suggest that, in subjects with atopic asthma, inhaled allergen causes trafficking of T lymphocytes to the bone marrow, and that in subjects who develop late responses and greater blood and airway eosinophilia after inhalation of allergen, there is a significant increase in the ability of bone marrow cells, particularly T lymphocytes, to produce IL-5.

摘要

对特应性哮喘患者进行吸入变应原激发试验会增加骨髓嗜酸性粒细胞祖细胞。白细胞介素-5(IL-5)特异性诱导嗜酸性粒细胞的生长和成熟。本研究检测了变应原激发试验对发生变应原诱导的单纯早期反应或早期和晚期哮喘反应(双重反应者)的哮喘患者骨髓中表达IL-5蛋白和IL-5 mRNA的总细胞数及CD3⁺细胞数的影响。变应原激发试验后24小时,双重反应者的血液和气道嗜酸性粒细胞增多明显高于早期反应者。两组骨髓CD3⁺细胞百分比均显著增加(p<0.005)。然而,双重反应者组和早期反应者组在骨髓IL-5 mRNA⁺(p<0.005)、CD3⁺(p<0.005)和IL-5 mRNA⁺CD3⁺(p<0.005)细胞增加方面存在显著差异。这些结果表明,在特应性哮喘患者中,吸入变应原会导致T淋巴细胞向骨髓迁移,并且在吸入变应原后出现晚期反应以及血液和气道嗜酸性粒细胞增多更明显的患者中,骨髓细胞尤其是T淋巴细胞产生IL-5的能力显著增加。

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