肺部铜绿假单胞菌感染的疫苗策略。

Behring Institute Mitteilungen Pub Date : 1997-02-01
A W Cripps, M L Dunkley, R L Clancy, J Kyd
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摘要

铜绿假单胞菌是一种在环境中普遍存在的细胞外机会性革兰氏阴性菌,与其他革兰氏阴性菌相比,感染这种细菌会导致严重的发病率和死亡率。感染风险特别高的患者是那些呼吸功能受损、接受重症监护支持和服用免疫损害药物的患者。一旦获得感染,就很难用化疗来根除,并且尝试接种预防感染的疫苗收效甚微。在过去的五年中,我们一直在研究粘膜免疫预防铜绿假单胞菌呼吸道感染的概念。在急性动物模型中的初步研究清楚地表明,用杀死的全细菌细胞制备的粘膜免疫可以在肺中诱导保护性免疫反应。随后的研究表明,保护性免疫机制依赖于抗原特异性CD4+ T细胞、肺泡巨噬细胞的激活、多态细胞(主要是中性粒细胞)的募集和激活、tnf - α、IL-1和IFN γ的受控分泌以及抗体的存在。我们假设这种保护性反应是由T细胞控制的。一种口服全杀死细胞制剂的临床前人体试验已经完成,没有不良副作用。一项针对支气管扩张患者的有限开放试验也已完成。初步分析结果表明,口服疫苗接种后,观察到特异性淋巴细胞对铜绿假单胞菌的反应。
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Vaccine strategies against Pseudomonas aeruginosa infection in the lung.

Pseudomonas aeruginosa is an environmentally ubiquitous, extracellular opportunistic gram-negative bacteria that causes significant morbidity and mortality to a disproportionately high degree for infections with this bacteria compared with other gram-negative bacteria. Patients at particular risk of infection are those with compromised respiratory function, in intensive-care support and taking immunocompromising pharmaceutical agents. Once acquired, infection is difficult to eradicate with chemotherapy and attempts to vaccinate against infection have been of little success. Over the past five years, we have pursued the concept of mucosal immunisation against respiratory infection with P. aeruginosa. Initial studies in an acute animal model clearly demonstrated that mucosal immunisation with a killed whole bacterial cell preparation could induce protective immune responses in the lung. Subsequent studies have shown that the protective immune mechanisms were dependent on antigen specific CD4+ T cells, the activation of alveolar macrophages, the recruitment and activation of polymorphs, predominantly neutrophils, the controlled secretion of TNF-alpha, IL-1 and IFN gamma and the presence of antibody. We have hypothesised that the protective response is under the control of T cells. A pre-clinical human trial of an oral whole killed cell preparation has been completed with no adverse side effects. A limited open trial in patients with bronchiectasis has also been completed. Preliminary analysis of the results has demonstrated that after oral vaccination, specific lymphocyte responses were observed to P. aeruginosa.

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