不可分型流感嗜血杆菌外膜囊泡的免疫原性及中耳炎鼠模型的保护能力。

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-10-05 Print Date: 2017-10-01 DOI:10.1128/CVI.00138-17
Linda E Winter, Stephen J Barenkamp
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引用次数: 13

摘要

革兰氏阴性菌产生的外膜囊泡(omv)富含多种外膜成分,包括主要外膜蛋白和次要外膜蛋白以及低脂糖。我们在鼠中耳炎模型中评估了非分型流感嗜血杆菌(NTHi) omv特异性抗血清的功能活性和NTHi omv作为疫苗抗原的保护能力。从三株表达HMW1/ hmw2的NTHi菌株中纯化出omv,其中两株也被改造成过表达Hia蛋白。在豚鼠中培养的omv特异性抗血清在调理噬细胞试验中评估了其介导杀伤代表性NTHi的能力。三种omv特异性抗血清介导65株中18株、65株中24株和65株无关表达HMW1/ hmw2的NTHi株中的30株的死亡。总的来说,它们介导了65株表达HMW1/ hmw2的菌株中的39株的杀伤。两种表达hia的omv特异性抗血清介导了25株中17株和25株无关的表达hia的NTHi株中的14株的杀伤。总的来说,它们介导了25株表达hia的菌株中的20株的死亡。用NTHi 12株原型株的omv免疫龙猫,并监测其球囊内攻毒后中耳感染的过程。所有对照动物均出现培养阳性中耳炎,三只HMW1/ hmw2免疫动物中的两只也出现了培养阳性中耳炎。所有经omv免疫的动物,无论是否补充HMW1/HMW2免疫,均能完全预防中耳炎。在该模型中,NTHi omv是第一个在NTHi菌株12攻击后提供完全无菌免疫保护的免疫原。这些数据表明,NTHi omv可能与HMW1/HMW2蛋白结合,具有作为保护性NTHi疫苗成分的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunogenicity of Nontypeable Haemophilus influenzae Outer Membrane Vesicles and Protective Ability in the Chinchilla Model of Otitis Media.

Immunogenicity of Nontypeable Haemophilus influenzae Outer Membrane Vesicles and Protective Ability in the Chinchilla Model of Otitis Media.

Immunogenicity of Nontypeable Haemophilus influenzae Outer Membrane Vesicles and Protective Ability in the Chinchilla Model of Otitis Media.

Outer membrane vesicles (OMVs) produced by Gram-negative bacteria are enriched in several outer membrane components, including major and minor outer membrane proteins and lipooligosaccharide. We assessed the functional activity of nontypeable Haemophilus influenzae (NTHi) OMV-specific antisera and the protective ability of NTHi OMVs as vaccine antigens in the chinchilla otitis media model. OMVs were purified from three HMW1/HMW2-expressing NTHi strains, two of which were also engineered to overexpress Hia proteins. OMV-specific antisera raised in guinea pigs were assessed for their ability to mediate killing of representative NTHi in an opsonophagocytic assay. The three OMV-specific antisera mediated killing of 18 of 65, 24 of 65, and 30 of 65 unrelated HMW1/HMW2-expressing NTHi strains. Overall, they mediated killing of 39 of 65 HMW1/HMW2-expressing strains. The two Hia-expressing OMV-specific antisera mediated killing of 17 of 25 and 14 of 25 unrelated Hia-expressing NTHi strains. Overall, they mediated killing of 20 of 25 Hia-expressing strains. OMVs from prototype NTHi strain 12 were used to immunize chinchillas and the course of middle ear infection was monitored following intrabullar challenge with the homologous strain. All control animals developed culture-positive otitis media, as did two of three HMW1/HMW2-immunized animals. All OMV-immunized animals, with or without supplemental HMW1/HMW2 immunization, were completely protected against otitis media. NTHi OMVs are the first immunogens examined in this model that provided complete protection with sterile immunity after NTHi strain 12 challenge. These data suggest that NTHi OMVs hold significant potential as components of protective NTHi vaccines, possibly in combination with HMW1/HMW2 proteins.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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