An HBC-vectored peptide-based cytomegalovirus vaccine

HBC 载体肽基巨细胞病毒疫苗

• 批准号: 8224073
• 负责人: Michael A McVoy
• 金额: $ 7.48万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-19 至 2014-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8224073
• 关键词: Antibody Formation; Antigens; Blocking Antibodies; Clinical; Complex; Congenital Abnormality; Core Protein; Cytomegalovirus; Cytomegalovirus Infections; Cytomegalovirus Vaccines; Development; Dose; Engineering; Epithelial; Epithelial Cells; Epitopes; Fibroblasts; Freund' s Adjuvant; Glass; Glycoproteins; Goals; Hepatitis B Virus; Human; Immunization; Keyhole Limpet Hemocyanin; Laboratories; Licensure; MF59; Mus; Oryctolagus cuniculus; Peptides; Proteins; Recombinants; Regimen; Research Personnel; Serum; Subunit Vaccines; Time; United States; Vaccine Research; Vaccines; Viral; Virion; Virus-like particle; Woman; Work; base; design and construction; human subject; neutralizing antibody; novel; novel vaccines; protective effect; response; skills; virus core

DESCRIPTION (provided by applicant): Human cytomegalovirus (CMV) is the major infectious cause of birth defects in the United States. Recent demonstration that the glycoprotein B (gB)/MF59 vaccine has 50% efficacy in protecting women against primary CMV infection is a landmark in CMV vaccine research. However, 50% efficacy may be insufficient for vaccine licensure. Thus, the challenge is to determine what can be added to a gB-based vaccine to increase efficacy to an acceptable level. Recent work from the PI's laboratory showed that CMV seropositive people have high levels of antibodies that neutralize viral entry into epithelial cells and that comparable levels are not achieved by the gB/MF59 vaccine. Epithelial entry-specific neutralizing epitopes reside within a virion glycoprotein complex consisting of gH, gL, UL128, UL130, and UL131 (gH/gL/UL128-131). The investigator's laboratory recently identified two peptide epitopes, one from UL130 and one from UL131, that are capable of eliciting potent epithelial entry-specific neutralizing responses. The co-PI has developed a novel platform for eliciting antibody responses to peptide epitopes. The desired peptides are engineered into an external loop of the hepatitis virus B core antigen (HBcAg) protein. The modified proteins self- assemble into virus-like particles (VLPs), which serve as potent immunogens and elicit strong antibody responses to the inserted peptide epitopes. We propose to engineer chimeric HBcAg proteins that contain the UL130 and UL131 peptide epitopes and evaluate the chimeric VLPs for their ability to elicit epithelial entry- specific neutralizing activities in mice. Optimal chimeric VLPs will be further evaluated for compatibility with the gB subunit vaccine. The results of the proposed studies may provide a novel vaccine strategy for advancement to clinical development. PUBLIC HEALTH RELEVANCE: Human cytomegalovirus is the major infectious cause of birth defects in the United States. We recently found that two peptide epitopes elicit high levels of antibodies that block viral entry into epithelial cells. Based on these results, a new vaccine strategy of expressing these peptides in the context of the hepatitis B virus core protein will be investigated. The results of the proposed studies may provide a novel vaccine strategy for advancement to clinical development.

描述（由申请人提供）：人类巨细胞病毒（CMV）是美国出生缺陷的主要传染性原因。最近证明糖蛋白B (gB)/MF59疫苗在保护妇女免受原发性巨细胞病毒感染方面有50%的效力，这是巨细胞病毒疫苗研究的一个里程碑。然而，50%的效力可能不足以获得疫苗许可。因此，面临的挑战是确定可以在基于gb的疫苗中添加什么以将效力提高到可接受的水平。PI实验室最近的工作表明，巨细胞病毒血清阳性的人具有高水平的抗体，可以中和病毒进入上皮细胞，而gB/MF59疫苗无法达到类似水平。上皮进入特异性中和表位位于由gH、gL、UL128、UL130和UL131组成的病毒粒子糖蛋白复合物中（gH/gL/UL128-131）。研究者的实验室最近发现了两个肽表位，一个来自UL130，一个来自UL131，它们能够引发有效的上皮进入特异性中和反应。co-PI开发了一种新的平台，用于引发对肽表位的抗体反应。所需的肽被设计成乙型肝炎病毒核心抗原（HBcAg）蛋白的外环。修饰后的蛋白质自我组装成病毒样颗粒（vlp），作为有效的免疫原，并引起对插入肽表位的强烈抗体反应。我们建议设计含有UL130和UL131肽表位的嵌合HBcAg蛋白，并评估嵌合VLPs在小鼠中引发上皮进入特异性中和活性的能力。将进一步评估最佳嵌合VLPs与gB亚单位疫苗的相容性。本研究结果可能为临床开发提供一种新的疫苗策略。