Multiplexed vaccine titer test

多重疫苗效价测试

• 批准号: 8085717
• 负责人: David Schwartz
• 金额: $ 30万
• 依托单位: SOLULINK BIOSCIENCES
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-06-10 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8085717
• 关键词: Adult; Antibodies; Antibody Formation; Antigens; Avidin; Binding; Biological Assay; Biological Response Modifiers; Biotin; Carbohydrates; Chemistry; Child; Childhood; Code; Color; Communicable Diseases; Complex; DNA; Detection; Development; Disease; Engineering; Enzyme-Linked Immunosorbent Assay; Enzymes; Exposure to; Fluorescence; Haemophilus influenzae type b bacteria; Health; Hepatitis B; Human poliovirus; Hydrazones; Immobilization; Immune response; Immunity; Immunization; Immunoassay; Immunoglobulin A; Immunoglobulin G; Immunoglobulin M; Immunoglobulins; Incubated; Infection; Infectious Agent; Injection of therapeutic agent; Label; Lead; Link; Magnetism; Manufacturer Name; Marketing; Measles; Measles-Mumps-Rubella Vaccine; Measures; Methods; Microspheres; Modality; Monitor; Mumps; Oligonucleotides; Organism; Parents; Patients; Pertussis; Phase; Phycoerythrin; Physicians; Poliomyelitis; Polysaccharides; Proteins; Reader; Reading; Reporter; Sampling; Schedule; Screening procedure; Sensitivity and Specificity; Serologic tests; Serotyping; Serum; Solutions; Specificity; Surface; System; Technology; Testing; Tetanus Toxoid; Toxoids; Vaccinated; Vaccination; Vaccines; Virion; Virus; Work; cost effective; crosslink; cytokine; design; immunoreactivity; magnetic beads; miniaturize; novel; novel vaccines; nucleic acid detection; phase 1 study; protocol development; research study; response; self assembly; tool; vaccine development; vaccine effectiveness; vaccine efficacy

DESCRIPTION (provided by applicant): Immunization efforts had all but eliminated childhood diseases such as polio, measles, and mumps by 1990, but the rapid introduction of new vaccines may paradoxically be promoting reemergence as complex injection schedules decrease compliance by parents and physicians. Vaccine manufacturers have responded with multivalent vaccines that provide single-injection protection against multiple agents. In addition to the measles, mumps and rubella vaccine (MMR), pentavalent combinations of diptheria toxoid, tetanus toxoid, and acellular pertussis (DTaP), inactivated polio virus (IPV), Haemophilus influenzae Type b (Hib), and/or hepatitis B (HepB), have been approved and others remain in development. The increasing range and multivalency of vaccines has created a need for cost-effective, highly multiplexed serological testing to determine antibody response to each component. New tests are needed both as screening assays to evaluate protection of each patient and as a tool for vaccine development to detect efficacy for each target in novel combinations. The traditional multiwell ELISA format immunoassay is laborious and poorly matched to multianalyte testing. Flow cytometric bead array immunoassays can replace such ELISA format assays with a miniaturized, multiplexed, rapid, sensitive and specific alternative. Despite the commercial potential of bead arrays for serology to monitor vaccination and infection, this market remains undeveloped compared to multiplexed sandwich immunoassays such as cytokine panels. A key limitation is the need to coat beads with diverse antigens, including proteins, polysaccharides, and whole virus particles, which requires a wide range of immobilization chemistries that must be independently optimized. Insofar as a comprehensive vaccination and infection assay will require >50-plex testing, the challenge of preparing robust and reproducible bead panels is a significant barrier. This submission proposes to overcome the limitations of current assays and expand the potential of the bead array immunoassay by the development of protocols that allow rapid multiplexing of diverse antigens employing novel chemistries and assay design to coat beads independent of whether the antigen is a carbohydrate, protein or virus. This will lead to kits for screening for responses to the full range of approved vaccines and for exposure to the most common infectious organisms. Importantly, these kits are completely dynamic and can be modified to reflect new vaccines, new infectious disease serotypes and/or newly discovered disease organisms. This platform has the potential to be engineered for use in the third world. PUBLIC HEALTH RELEVANCE: Multivalent Vaccine Titer Test A standardized method to rapidly determine the level of response to multivalent vaccines has not been developed. Availability of a standardized test would allow more efficient development of new multivalent vaccines as well as determining effectiveness of vaccines in vaccinated children and adults. In this submission we propose the development of a platform technology that will allow rapid, cost effective and sensitive standardized testing for vaccine efficacy.

描述（由申请人提供）：到1990年，免疫工作几乎消除了小儿麻痹症、麻疹和腮腺炎等儿童疾病，但新疫苗的快速引入可能矛盾地促进了重新出现，因为复杂的注射时间表降低了父母和医生的依从性。疫苗制造商已采用多价疫苗作为应对措施，这种疫苗可提供单次注射保护，抵御多种病原体。除了麻疹、腮腺炎和风疹疫苗（MMR）外，白喉类毒素、破伤风类毒素和无细胞百日咳（DTaP）、灭活脊髓灰质炎病毒（IPV）、b型流感嗜血杆菌（Hib）和/或乙型肝炎（HepB）的五价组合疫苗已获批准，其他疫苗仍在开发中。疫苗的范围和多价性日益扩大，因此需要进行具有成本效益的、高度多重的血清学检测，以确定对每种成分的抗体反应。需要新的检测方法，既可以作为评估每位患者的保护作用的筛选分析方法，也可以作为开发疫苗的工具，以检测新组合中每个靶点的效力。