Development of a vaccine for prevention of Haemophilus influenzae otitis media

预防流感嗜血杆菌中耳炎疫苗的研制

• 批准号: 8260846
• 负责人: Stephen J. Barenkamp
• 金额: $ 30万
• 依托单位: SAINT LOUIS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8260846
• 关键词: Acute; Address; Adenovirus Vector; Adenoviruses; Adhesions; Adult; Affinity; Amino Acid Sequence; Animals; Antibodies; Antibody Formation; Antigens; Bacteria; Bacterial Adhesins; Bacterial Antigens; Bacterial Proteins; Biological Assay; Bordetella pertussis; Child; Chinchilla (genus); Collection; Data; Development; Disease; Epithelial Cells; Epitopes; Eukaryotic Cell; Experimental Models; Family; Genes; Goals; Grant; Haemophilus Vaccines; Haemophilus influenzae; Health; Hemagglutinin; Hemophilus; Human; Immune Sera; Immune response; Immunization; Infection; Laboratories; Maps; Mediating; Modeling; Molecular Weight; Monoclonal Antibodies; Nontypable Haemophilus influenza; Otitis; Otitis Media; Pertussis; Predisposition; Preparation; Prevention; Protein Family; Proteins; Recombinant Fusion Proteins; Recombinant Vaccines; Recombinants; Role; Serum; Serum Proteins; Surface; Vaccine Antigen; Vaccines; Work; bactericide; base; defined contribution; disorder prevention; domain mapping; ear infection; immunogenic; immunogenicity; innovation; killings; novel; prototype; public health relevance; vaccine candidate; vaccine development; vector

DESCRIPTION (provided by applicant): Otitis media and other illnesses caused by nontypeable Haemophilus influenzae (NTHi) remain significant health problems for children and a vaccine for prevention of disease is much needed. Our long-term objectives are to identify surface-exposed antigens of NTHi that are important in a protective immune response, and ultimately, to determine whether a vaccine composed of such antigens would be protective against NTHi disease. In early work, we identified the HMW1/HMW2 and Hia families of proteins as major targets of the human antibody response following natural infection. We later demonstrated a critical role for both protein families in adhesion of NTHi to human eukaryotic cells. Virtually all NTHi express either HMW/HMW2-like or Hia-like adhesins. We later demonstrated the vaccine potential of prototype HMW1/HMW2 proteins in immunization studies in which chinchillas immunized parenterally were protected against NTHi otitis media caused by the homologous strain. We also demonstrated that naturally-acquired human antibodies specific for the HMW1/HMW2-like proteins and polyclonal antisera raised against these proteins are opsonophagocytic for both homologous and heterologous HMW1/HMW2-expressing strains. In more recent work on the Hia proteins, we demonstrated that antibodies specific for the Hia-like proteins are also opsonophagocytic for homologous and heterologous Hia-expressing NTHi. Taken together, these data suggest that proteins from both the HMW1/HMW2 and Hia families, most likely in combination, deserve serious consideration as vaccine candidates for prevention of NTHi disease. Direct mucosal immunization is thought by many experts in the field to be critical to development of a successful otitis media vaccine. In our very recent work, we constructed recombinant adenovirus vectors expressing either HMW1/HMW2 or Hia proteins and demonstrated the immunogenicity of these constructs in the chinchilla otitis model. In the proposed work, we will build upon these earlier studies and determine whether the HMW1/HMW2- and Hia-like proteins can move forward as viable NTHi vaccine candidates. First, we will define the contribution of human antibodies produced against the HMW1/HMW2- and Hia-like proteins to the opsonophagocytic activity that develops in convalescent sera of children with acute NTHI otitis media. Next, we will map the regions of the HMW1/HMW2- and Hia-like proteins that express epitopes recognized by antibodies capable of mediating opsonophagocytic activity against both homologous and heterologous NTHi. Finally, we will assess the ability of recombinant adenovirus vectors expressing the HMW1/HMW2- or Hia-like proteins to provide protection against NTHi disease in the chinchilla model of experimental otitis media. Our proposed studies are innovative for the field both in terms of the promising vaccine antigens under study and in terms of the novel mucosal immunization strategy being investigated. The resulting information will move us further towards our ultimate goal of developing effective vaccines for prevention of NTHi otitis media and other diseases in young children. PUBLIC HEALTH RELEVANCE: Ear infections caused by nontypeable Haemophilus influenzae bacteria are a major problem for children everywhere. The objective of our work is to develop a vaccine for prevention of these Haemophilus ear infections. We previously identified two related bacterial proteins that are very promising vaccine candidates and we will further assess their vaccine potential in the studies proposed in this grant.

描述（由申请人提供）：由不可分型的流感嗜血杆菌（NTHi）引起的中耳炎和其他疾病仍然是儿童的重大健康问题，非常需要预防疾病的疫苗。我们的长期目标是确定在保护性免疫反应中重要的NTHi表面暴露抗原，并最终确定由这些抗原组成的疫苗是否能预防NTHi疾病。在早期工作中，我们确定了HMW1/HMW2和Hia家族蛋白是自然感染后人类抗体反应的主要靶点。我们后来证明了这两个蛋白家族在NTHi粘附到人类真核细胞中的关键作用。几乎所有的NTHi都表达HMW/ hmw2样或hia样粘附素。我们随后在免疫研究中证明了原型HMW1/HMW2蛋白的疫苗潜力，在免疫研究中，经肠外免疫的龙猫可以免受同源菌株引起的NTHi中耳炎。我们还证明了自然获得的人抗体特异性针对HMW1/ hmw2样蛋白和针对这些蛋白的多克隆抗血清对同源和异源表达HMW1/ hmw2的菌株都具有调节噬细胞作用。在最近对Hia蛋白的研究中，我们证明了针对Hia样蛋白的特异性抗体对同源和异源表达Hia的NTHi也具有调理噬细胞作用。综上所述，这些数据表明，来自HMW1/HMW2和Hia家族的蛋白质（很可能是组合）值得认真考虑作为预防NTHi疾病的候选疫苗。许多专家认为，直接粘膜免疫是研制成功中耳炎疫苗的关键。在我们最近的工作中，我们构建了表达HMW1/HMW2或Hia蛋白的重组腺病毒载体，并在栗鼠中耳炎模型中证明了这些构建物的免疫原性。在拟议的工作中，我们将建立在这些早期研究的基础上，并确定HMW1/HMW2-和hia样蛋白是否可以作为可行的NTHi候选疫苗向前发展。首先，我们将确定在患有急性NTHI中耳炎的儿童恢复期血清中产生的针对HMW1/HMW2-和hia样蛋白的人抗体对调节噬细胞活性的贡献。接下来，我们将绘制HMW1/HMW2和hia样蛋白表达表位的区域，这些表位能够被能够介导抗同源和异源NTHi的调节噬细胞活性的抗体识别。最后，我们将评估表达HMW1/HMW2或hia样蛋白的重组腺病毒载体在实验性中耳炎鼠模型中对NTHi疾病的保护能力。我们提出的研究在研究有前途的疫苗抗原和正在研究的新的粘膜免疫策略方面都是该领域的创新。由此产生的信息将使我们进一步实现我们的最终目标，即开发有效的疫苗，以预防NTHi中耳炎和幼儿其他疾病。