Signatures of Immunity on the Antigenic Diversity of Pathogens

病原体抗原多样性的免疫特征

• 批准号: 8125740
• 负责人: Sarah Cobey
• 金额: $ 4.84万
• 依托单位: HARVARD SCHOOL OF PUBLIC HEALTH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2013-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8125740
• 关键词: Affect; Alleles; Antigenic Diversity; Case Series; Cellular Immunity; Computer Simulation; Effectiveness; Epidemiology; Epitopes; Equation; Equilibrium; Exposure to; Frequencies; Genetic; Goals; Heterogeneity; Human; Humoral Immunities; Immune; Immunity; Individual; Infection; Infectious Disease Immunology; Influenza; Influenza A Virus, H1N1 Subtype; Intervention; Knowledge; Light; Measures; Mediating; Methods; Modeling; Natural Immunity; Neisseria meningitidis; Outcome; Parainfluenza; Pattern; Phenotype; Population; Positioning Attribute; Prevalence; Process; Recording of previous events; Research; Research Personnel; Research Training; Role; Scientist; Serotyping; Shapes; Streptococcus pneumoniae; Techniques; Testing; Time; Training; Vaccination; Validation; Variant; Work; adaptive immunity; base; cross immunity; effective intervention; experience; improved; influenzavirus; mathematical model; parainfluenza virus; pathogen; predictive modeling; response; transmission process

DESCRIPTION (provided by applicant): Many human pathogens show extensive antigenic diversity. Immunity from infection with one antigenic variant is often partially protective against infection with another antigenic variant, resulting in competition between antigenically similar strains for susceptible hosts. Understanding the immunological mechanisms underlying this competition is an important step in predicting strain dynamics, including such questions as whether a new antigenic variant will drive residents extinct, and how vaccination against some strains will affect competing strains that aren't targeted. Classic models of strain competition predict negative frequency-dependent selection driven by long-lasting, strain-specific immunity. Though sometimes a useful approximation, these simple models shed little light on how other known mechanisms of immunity might explain subtle differences in patterns of antigenic diversity of related pathogens. The goal of this project is to test the general hypothesis that different kinds of immunity shape population-level patterns in pathogen diversity. The first aim is to assess the roles of innate and antibody-based immunity in generating the patterns of antigenic diversity in two common bacterial pathogens, Streptococcus pneumoniae (pneumococcus) and Neisseria meningitidis (meningococcus). The respective contributions of each kind of immunity will be evaluated by comparing the observed prevalence of major antigenic types with results from an individual-based model in which the strength, breadth, and duration of heterologous immunity are varied in accordance with each type of immunity. The second aim uses the same three factors to infer the contributions of innate, cellular, and humoral immunity to the dynamics of two viruses, influenza and parainfluenza. The three factors will be estimated directly by fitting models of ordinary differential equations to time series of cases of each major antigenic type (serotypes 1-3 of parainfluenza and type A (subtype H3N2), A (H1N1), and B of influenza). The third aim explores to what extent differences between individual hosts might influence the outcomes of strain competition. These differences might have a genetic origin, such as hosts' MHC type I and II alleles, or derive from hosts' specific infection histories; preliminary work suggests highly biased responses to particular epitopes promote coexistence of antigenic types. To measure the effects of heterogeneous responses, individual-based models will be used to compare equilibrium and nonequilibrium diversity levels under assumptions of heterogeneity and homogeneity. This three-year postdoctoral research training plan will improve the investigator's understanding of the immunology of infectious diseases, the ways in which different immune mechanisms can affect host-pathogen dynamics, and which modeling approaches are appropriate in different situations. Augmented by a diverse set of professional training opportunities, this experience will prepare the investigator for an independent research position. This knowledge will ultimately be useful to the investigator and other scientists seeking to develop predictive models of the dynamics of competing pathogen strains. PUBLIC HEALTH RELEVANCE: Many common pathogens of humans show extensive antigenic diversity. The purpose of the proposed research is to use computational and mathematical models to test how different kinds of immunity mediate this diversity. This information will be useful for developing effective intervention strategies.

描述（由申请人提供）：许多人类病原体表现出广泛的抗原多样性。对一种抗原变异感染的免疫力通常对另一种抗原变异感染具有部分保护作用，导致抗原相似的菌株之间对易感宿主的竞争。了解这种竞争背后的免疫学机制是预测菌株动态的重要一步，包括诸如新的抗原变异是否会导致居民灭绝，以及针对某些菌株的疫苗接种如何影响非靶向的竞争菌株等问题。菌株竞争的经典模型预测由持久的菌株特异性免疫驱动的负频率依赖选择。虽然这些简单的模型有时是有用的近似值，但对于其他已知的免疫机制如何解释相关病原体抗原多样性模式的细微差异，这些简单的模型几乎没有说明。这个项目的目标是检验一个普遍的假设，即不同种类的免疫在病原体多样性中形成群体水平的模式。第一个目的是评估先天免疫和基于抗体的免疫在产生两种常见细菌病原体——肺炎链球菌（肺炎球菌）和脑膜炎奈瑟菌（脑膜炎球菌）的抗原多样性模式中的作用。将通过比较观察到的主要抗原类型的流行率与基于个体的模型的结果来评估每种免疫的各自贡献，在该模型中，异源免疫的强度、广度和持续时间根据每种免疫类型而变化。第二个目标使用相同的三个因素来推断先天、细胞和体液免疫对两种病毒（流感和副流感）动力学的贡献。这三个因素将通过将常微分方程模型拟合到每种主要抗原型（副流感血清型1-3和流感A型（H3N2亚型）、A （H1N1）和B型）病例的时间序列来直接估计。第三个目的是探讨个体宿主之间的差异在多大程度上可能影响品系竞争的结果。这些差异可能有遗传来源，如宿主的MHC I型和II型等位基因，或源于宿主的特定感染史；初步研究表明，对特定表位的高度偏倚反应促进了抗原类型的共存。为了测量异质性响应的影响，将使用基于个体的模型来比较异质性和同质性假设下的平衡和非平衡多样性水平。这项为期三年的博士后研究培养计划将提高研究者对传染病免疫学的认识，了解不同免疫机制对宿主-病原体动力学的影响方式，以及在不同情况下采用何种建模方法。通过多样化的专业培训机会，这一经验将使研究者为独立的研究职位做好准备。这些知识最终将有助于研究者和其他科学家寻求开发竞争病原体菌株动力学的预测模型。