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一种与铜绿假单胞菌OprF的肽10同源的P5肽,在没有可检测到的肽特异性抗体的情况下,可增强急性感染大鼠肺中不可分型流感嗜血杆菌的清除。

A P5 peptide that is homologous to peptide 10 of OprF from Pseudomonas aeruginosa enhances clearance of nontypeable Haemophilus influenzae from acutely infected rat lung in the absence of detectable peptide-specific antibody.

作者信息

Webb D C, Cripps A W

机构信息

The Gadi Research Center, Faculty of Applied Science and Design, University of Canberra, Canberra City, Australian Capital Territory 2601, Australia.

出版信息

Infect Immun. 2000 Jan;68(1):377-81. doi: 10.1128/IAI.68.1.377-381.2000.

Abstract

Nontypeable Haemophilus influenzae (NTHi) is an opportunistic pathogen associated with otitis media and the exacerbation of chronic bronchitis. This study reports the vaccine potential of three peptides representing conserved regions of the NTHi P5 outer membrane protein which have been fused to a promiscuous measles virus F protein T-cell eptitope (MVF). The peptides correspond to a region in surface loop one (MVF/L1A), the central region of loop four (MVF/L4), and a C-terminal region homologous to peptide 10 of OprF from Pseudomonas aeruginosa (MVF/H3). Immunization of rats with MVF/H3 was the most efficacious in significantly reducing the number of viable NTHi in both the broncho-alveolar lavage fluid (74%) and lung homogenates (70%), compared to control rats. Importantly, despite significantly increased rates of clearance, immunization with MVF/H3 elicited poor antibody responses, suggesting that cell-mediated rather than humoral responses play an important role in the enhanced clearance of NTHi in this model.

摘要

非分型流感嗜血杆菌(NTHi)是一种与中耳炎和慢性支气管炎加重相关的机会致病菌。本研究报告了三种代表NTHi P5外膜蛋白保守区域的肽与一种通用麻疹病毒F蛋白T细胞表位(MVF)融合后的疫苗潜力。这些肽分别对应表面环1中的一个区域(MVF/L1A)、环4的中央区域(MVF/L4)以及与铜绿假单胞菌OprF的肽10同源的C端区域(MVF/H3)。与对照大鼠相比,用MVF/H3免疫大鼠在显著减少支气管肺泡灌洗液(74%)和肺匀浆(70%)中活的NTHi数量方面最为有效。重要的是,尽管清除率显著提高,但用MVF/H3免疫引发的抗体反应较差,这表明在该模型中,细胞介导而非体液反应在增强NTHi清除中起重要作用。

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