Structure-function analysis of infection- and vaccine-induced B-cell repertoires

感染和疫苗诱导的 B 细胞库的结构功能分析

• 批准号: 8303235
• 负责人: STEPHEN COPLAN HARRISON
• 金额: $ 216.85万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-01 至 2016-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8303235
• 关键词: Adjuvant; Affinity; Antibodies; Antigenic Variation; Antigens; Archives; B cell repertoire; B-Lymphocytes; Clinical; Collaborations; Complex; Cryoelectron Microscopy; Data; Electron Microscopy; Epitope Mapping; Epitopes; Equipment and supply inventories; Foundations; Genes; Genetic; Goals; Hemagglutinin; Human; Immune response; Immunization; Immunology; Inactivated Vaccines; Individual; Infection; Influenza Hemagglutinin; Lead; Link; Methods; Molecular; Pathway interactions; Principal Investigator; Property; Publishing; Reagent; Recombinants; Research Personnel; Role; Sampling; Series; Specificity; Structure; Sum; Surface Antigens; Technology; Testing; Time; Vaccinated; Vaccination; Vaccine Design; Vaccines; Viral Antigens; Work; cross reactivity; design; experience; improved; influenza virus vaccine; influenzavirus; innovation; method development; movie; novel; novel vaccines; pathogen; programs; response; stem; structural biology; technological innovation; three dimensional structure; vaccine development; virology

DESCRIPTION (provided by applicant): Antigenic variation underlies a large number of the most critical problems now facing vaccine development. Influenza virus is an ideal subject for tackling this issue: it is the most variable pathogen against which we can effectively vaccinate, but its principal surface antigen varies so rapidly that new vaccines must be introduced almost yearly. We propose to use innovative analyses of B-cell repertoires and new possibilities in structural studies to understand the structural and immunological mechanisms underlying cross reactivity and immunodominance, as a foundation for designing immunogens that will elicit a more broadly neutralizing response than those currently in use. We will test the following three hypotheses, to which the three Aims of each Project correspond. (1) The B-cell repertoires elicited by inactivated vaccines and by infection differ in degree of polyclonal activation and breadth of neutralization; the repertoires elicited by immunization with adjuvanted and non-adjuvanted TIV differ because adjuvant increases the breadth of recognized epitopes. (2) Broadly reactive Abs, including those recognizing the heterosubtypic stem epitope, are less frequent after true primary than after secondary TIV immunization due to broadening of the response by multiple HA stimulations. (3) Efficient induction of Abs against a desired epitope requires: (a) proliferation of a favorable germline Ab and (b) an affinity maturation pathway to a desired final specificity; there are preferred germline precursors and maturation pathways for Abs targeting particular epitopes. The group of investigators that joins in this proposal brings together strengths in immunology, virology, structural biology, and vaccine development. The principal investigators have worked closely and effectively together in past collaborations.

描述（由申请人提供）：抗原变异是疫苗开发目前面临的大量最关键问题的基础。流感病毒是解决这个问题的理想对象：它是我们可以有效接种的最可变的病原体，但其主要表面抗原变化如此之快，以至于几乎每年都必须引入新疫苗。我们建议使用创新的分析B细胞库和新的可能性，在结构研究中了解交叉反应和免疫优势的结构和免疫学机制，作为设计免疫原，将引起更广泛的中和反应比目前使用的基础。我们将测试以下三个假设，每个项目的三个目标对应。(1)灭活疫苗和感染引起的B细胞库在多克隆活化程度和中和宽度方面不同;用佐剂和非佐剂TIV免疫引起的库不同，因为佐剂增加了识别表位的宽度。(2)广泛反应性抗体，包括识别异亚型茎表位的抗体，在真正的初次免疫后比在二次TIV免疫后更不常见，这是由于多次HA刺激扩大了应答。(3)针对所需表位的Ab的有效诱导需要：（a）有利的种系Ab的增殖和（B）达到所需最终特异性的亲和力成熟途径;对于靶向特定表位的Ab，存在优选的种系前体和成熟途径。加入这项提案的研究人员小组汇集了免疫学、病毒学、结构生物学和疫苗开发方面的优势。主要研究人员在过去的合作中密切有效地合作。