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支气管阻塞中流感嗜血杆菌抗原的体内和体外反应

In vivo and in vitro reactions to antigens of Haemophilus influenzae in bronchial obstruction.

作者信息

Clarke C W

出版信息

Br J Dis Chest. 1979 Oct;73(4):373-81.

PMID:95481
Abstract

The frequency of precipitating antibody to heat-labile (H(1--2) and heat-stable (HCW and HCF) antigens of Haemophilus influenzae was determined in patients with asthma, chronic bronchitis, cystic fibrosis and bronchiectasis and compared with that in a control group. This showed that the immune response of asthmatic patients to heat-stable antigens was different from that to the heat-labile antigens. Exposure to antigens of H. influenzae is common in all the disease groups. Skin test reactions having the time course and macroscopic appearance of Type I (immediate) and Type III (late) were obtained after prick and intracutaneous skin testing with HCW antigen in varying concentrations in a group of patients with asthma, chronic bronchitis or cystic fibrosis and in a control group. It is suggested that IgE and short-term sensitizing IgG antibodies may be responsible for the immediate reactions while activation of the alternative pathway of complement by endotoxin contained in HCW could be responsible for the late reactions. HCW antigens were shown to release histamine from non-sensitized human leucocytes; HCW and HCF antigens were shown to release histamine from non-sensitized human lung. None of the antigens tested had an effect on beta-receptors in tracheal preparations. It is proposed that these reactions may contribute to the pathogenicity of H. influenzae in the lower respiratory tract.

摘要

测定了哮喘、慢性支气管炎、囊性纤维化和支气管扩张患者针对流感嗜血杆菌不耐热(H(1--2))和耐热(HCW和HCF)抗原的沉淀抗体频率,并与对照组进行了比较。结果表明,哮喘患者对耐热抗原的免疫反应与对不耐热抗原的免疫反应不同。在所有疾病组中,接触流感嗜血杆菌抗原都很常见。在一组哮喘、慢性支气管炎或囊性纤维化患者以及对照组中,用不同浓度的HCW抗原进行针刺和皮内皮肤试验后,获得了具有I型(即刻)和III型(迟发)时间进程和宏观外观的皮肤试验反应。提示IgE和短期致敏IgG抗体可能是即刻反应的原因,而HCW中所含内毒素激活补体替代途径可能是迟发反应的原因。已证明HCW抗原可从非致敏人白细胞中释放组胺;已证明HCW和HCF抗原可从非致敏人肺中释放组胺。所测试的抗原均对气管制剂中的β受体无影响。有人提出,这些反应可能有助于流感嗜血杆菌在下呼吸道的致病性。

相似文献

1
In vivo and in vitro reactions to antigens of Haemophilus influenzae in bronchial obstruction.支气管阻塞中流感嗜血杆菌抗原的体内和体外反应
Br J Dis Chest. 1979 Oct;73(4):373-81.
2
Antigens of Haemophilus influenzae.流感嗜血杆菌的抗原
Clin Allergy. 1977 Jan;7(1):41-7. doi: 10.1111/j.1365-2222.1977.tb01423.x.
3
Bronchial hyperresponsiveness and bacterial respiratory infections.
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Haemophilus influenzae release histamine and enhance histamine release from human bronchoalveolar cells. Examination of patients with chronic bronchitis and controls.流感嗜血杆菌释放组胺并增强人支气管肺泡细胞的组胺释放。慢性支气管炎患者与对照的检查。
APMIS. 1995 Nov;103(11):806-12.
5
Haemophilus influenzae localized in epithelial cell layers is shielded from antibiotics and antibody-mediated bactericidal activity.定位于上皮细胞层的流感嗜血杆菌可免受抗生素和抗体介导的杀菌活性的影响。
Microb Pathog. 1999 May;26(5):249-62. doi: 10.1006/mpat.1998.0269.
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Precipitating antibody to antigens of Pseudomonas aeruginosa in chronic obstructive lung disease.
Clin Allergy. 1977 Nov;7(6):527-37. doi: 10.1111/j.1365-2222.1977.tb01483.x.
7
Haemophilus influenzae and the beta-adrenergic system: a review.流感嗜血杆菌与β-肾上腺素能系统:综述
Vet Res Commun. 1984 Feb;8(1):1-14. doi: 10.1007/BF02214689.
8
Endotoxin from Haemophilus influenzae enhances IgE-mediated and non-immunological histamine release.
Allergy. 1990 Jan;45(1):10-7. doi: 10.1111/j.1398-9995.1990.tb01078.x.
9
Effects of vaccination with Haemophilus influenzae on adrenoceptor function of tracheal and parenchymal strips.流感嗜血杆菌疫苗接种对气管和实质组织条带肾上腺素能受体功能的影响。
J Pharmacol Exp Ther. 1980 Dec;215(3):691-6.
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Basophil-bound IgE and serum IgE directed against Haemophilus influenzae and Streptococcus pneumoniae in patients with chronic bronchitis during acute exacerbations.慢性支气管炎患者急性加重期嗜碱性粒细胞结合的IgE以及针对流感嗜血杆菌和肺炎链球菌的血清IgE 。
APMIS. 1996 Jan;104(1):61-7.

引用本文的文献

1
Antigen of Haemophilus influenzae in bronchial tissue.支气管组织中的流感嗜血杆菌抗原。
Thorax. 1981 Sep;36(9):665-8. doi: 10.1136/thx.36.9.665.
2
Bacterial antigens stimulate the production of histamine releasing factor (HRF) by lymphocytes from intrinsic asthmatic patients.细菌抗原刺激内源性哮喘患者淋巴细胞产生组胺释放因子(HRF)。
Clin Exp Immunol. 1986 Jan;63(1):241-8.