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中文摘要
翻译
该项目将利用DNA/ALVAC-HIV疫苗平台诱导持久训练单核细胞记忆的能力,结合进化支AE (A244株)v1缺失HIV-gp160引物和新型v1缺失HIV- gp120/明铝蛋白增强剂。从gp120包膜中删除V1将经过特殊设计,以减少抗体干扰,并引发高水平的V2抗体,V2是RV144风险的主要相关因素。氢氧化铝将被用作佐剂,因为它能够最大限度地诱导训练免疫(通过其诱导IL-1B的能力)和CD4+ t细胞反应,这构成了RV144中HIV感染风险降低的次要关联。本提案的总体目标是在GMP条件下设计和生产一种新型HIV - v1缺失的A244 gp160 (A244 DeltaV1 gp160) DNA疫苗和一种新型HIV - v1缺失的A244 gp120 (A244 DeltaV1 gp120),用于I期人类HIV疫苗试验。这些免疫原将首先在猕猴中进行测试,以评估这种方法是否也能在人类中诱导持久的、非干扰的抗体、先天单核细胞记忆和具有低炎症特征的适应性CD4+ t细胞。研究保护性单核细胞,或NK记忆训练免疫,将证明对对抗其他传染病和癌症有益。从无脊椎动物进化保守,训练免疫是人类免疫系统的一种古老特征,由单核细胞的持久表观遗传重编程定义,提供抵抗病原体的第一道防线。这不仅将导致生产和测试一种新的艾滋病毒疫苗,而且还将彻底研究免疫系统与人类相似的非人类灵长类动物(NHP)未开发的宿主保护性免疫反应。
英文摘要
The project will exploit the DNA/ALVAC-HIV vaccine platform's ability to induce lasting trained monocyte memory in combination with a clade AE (A244 strain) V1-deleted HIV-gp160 prime and a novel V1-deleted HIV gp120/alum protein boost. The deletion of V1 from the gp120 envelope will be specially engineered to minimize antibody interference and elicit a high level of antibodies to V2, the primary correlate of risk in RV144. Alum hydroxide will be used as adjuvant for its ability to maximize the induction of trained immunity (through its ability to induce IL-1B) and CD4+ T-cell responses that constituted the secondary correlate of decreased risk of HIV acquisition in RV144. The overall objective of this proposal is to design and produce both a novel HIV V1-deleted A244 gp160 (A244 DeltaV1 gp160) DNA vaccine and a novel HIV V1-deleted A244 gp120 (A244 DeltaV1 gp120) in GMP conditions for testing in a phase I human HIV vaccine trial. These immunogens will first be tested in macaques to assess whether this approach also induces long-lasting, non-interfering antibodies, innate monocyte memory, and adaptive CD4+ T-cells with a low inflammatory profile in humans. The investigation of protective monocyte, or NK memory trained immunity, will prove beneficial in combatting additional infectious diseases and cancer. Evolutionary conserved from invertebrates, trained immunity is an ancient trait of the human immune system that is defined by durable epigenetic reprogramming of monocytes, providing the first line of defense against pathogens .This will lead not only to the production and testing of a novel HIV vaccine, but also to the thorough investigation of unexplored host protective immune responses in non-human primates (NHP) whose immune system mirrors that of humans.
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INDUCTION OF SIV-SPECIFIC CD8+ LYMPHOCYTES
  • 批准号:
    6970744
  • 项目类别:
  • 资助金额:
    $4.72万
  • 财政年份:
    2004
  • 负责人:
    Genoveffa Franchini
  • 依托单位:
INDUCTION OF SIV-SPECIFIC CD8+ INTRAEPITHELIAL LYMPHOCYTES
  • 批准号:
    6939813
  • 项目类别:
  • 资助金额:
    $6.16万
  • 财政年份:
    2003
  • 负责人:
    Genoveffa Franchini
  • 依托单位:
VACCINE STRATEGIES FOR INDUCTION OF ANTI-HIV MUCOSAL IMMUNE RESPONSES
  • 批准号:
    6939800
  • 项目类别:
  • 资助金额:
    $6.16万
  • 财政年份:
    2003
  • 负责人:
    Genoveffa Franchini
  • 依托单位:
DEVELOPMENT OF AN HIV-1 AND HTLV-1 VACCINE IN ANIMAL MODELS
  • 批准号:
    2463673
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    --
  • 负责人:
    Genoveffa Franchini
  • 依托单位:
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