在粘膜部位对抗病原体的生物技术方法

C. Kelly, D. Medaglini, Justine S. Younson, G. Pozzi
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引用次数: 7

摘要

宿主与病原体之间的相互作用大多发生在宿主粘膜表面。许多病原体,如人类免疫缺陷病毒(HIV),通过粘膜进入,而其他病原体,包括念珠菌、变形链球菌和幽门螺杆菌,必须在粘膜上建立,才能对宿主造成损害。图13.1概述了控制粘膜表面病原体和感染性疾病的总体策略。这些措施主要包括接种疫苗和使用抗微生物化学疗法,特别是抗生素,这两种方法都对传染病产生了巨大影响(Cohen, 2000年)。随着疫苗和抗生素的出现,被动免疫的使用越来越少,但对于治疗免疫能力低下的患者越来越重要(Hammarstrom, 1999年),而局部杀微生物剂的开发和使用被认为是预防艾滋病毒感染的潜在重要手段(Lange等人,1993年)。然而,粘膜部位的病原体对这些措施提出了特殊的问题,例如,抗生素可以非常有效地清除全身感染,但不能影响病原体的粘膜携带。有限数量的疫苗可诱导保护性粘膜反应,目前还没有针对感染所有表面的几种微生物的疫苗。这些观察结果,加上对抗生素耐药性蔓延的担忧(Hawkey, 1998;Irvin和Bautista, 1999)刺激了对其他抗菌策略的研究以及对现有方法的改进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biotechnological Approaches to Fight Pathogens at Mucosal Sites
Most interactions between host and pathogens occur at the host mucos al surfaces. Many pathogens, such as the human immunodeficiency virus (HIV), gain entry via the mucosa while others, including Candida, Streptococcus mutans and Helicobacter pylori , must become established at the mucosa to cause damage to the host. Strategies aimed at controlling pathogens at mucosal surfaces and infectious diseases in general are summarized in Figure 13.1. These include primarily vaccination and the use of antimicrobial chemotherapy, particularly antibiotics, which have both had an enormous impact on infectious disease (Cohen, 2000). Passive immunization has been used less with the advent of vaccines and antibiotics but is of increasing importance for treatment of immunocornpromised patients (Hammarstrom, 1999) whilst the development and use of topical microbicides is regarded as a potentially important means of preventing infection with HIV (Lange et al., 1993). Pathogens at mucosa( sites, however, present particular problems for these measures, e.g. antibiotics can be very effective in clearing systemic infections while being unable to affect mucosal carriage of the pathogen. A limited number of vaccines induce protective mucosal responses and vaccines are not yet available for several microorganisms that infect rnucos al surfaces. These observations, together with concern over the spread of antibiotic resistance (Hawkey, 1998; Irvin and Bautista, 1999), have stimulated investigation of additional antimicrobial strategies as well as refinement of existing approaches.
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