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Membrane-bound immunomodulators as adjuvants in a cell culture-based avian influenza vaccine.

机译:膜结合免疫调节剂作为基于细胞培养的禽流感疫苗的佐剂。

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摘要

Inactivated viral vaccines often generate suboptimal immune responses. Adjuvants are incorporated into vaccines to increase their immunogenicity, however currently available adjuvants have shortcomings which have limited their use in human and veterinary medicine. This necessitates the development of new adjuvants and delivery systems. Cytokines have been extensively tested as adjuvants in vaccines but challenges such as diffusion from antigen, short half-lives and production costs have been encountered. To address this, we developed a technology that efficiently produces inactivated, whole-virus influenza vaccine bearing membrane-bound cytokines. Tethering the cytokine to the antigen of interest keeps the immunomodulator in close contact with the antigen ensuring that immune cells recruited or activated by the adjuvant react with the antigen as well. Influenza can be used to test this model since its surface proteins HA and NA contain conserved signal sequences that direct these proteins to the infected cell surface where they are picked up by budding virions. Plasmids containing cytokines fused to these signal sequences are introduced into MDCK cell lines and, upon expression, the fusion proteins are directed to the lipid islands on the cell membrane. When the cells are infected with influenza, new virus assembles at the lipid islands and incorporates the fusion proteins into the viral envelope. Furthermore, this mammalian cell culture-based production system bypasses many of the current limitations found in the egg-based influenza vaccine production system.;This model was tested in a chicken model using membrane-bound C3d, GMCSF, IL2 and IL4 as adjuvants. GMCSF adjuvanted vaccines delivered subcutaneously and C3d adjuvanted vaccines delivered subcutaneously and intranasally resulted in significantly higher antibody titers than vaccinating with inactivated virus alone. Vaccination with C3d adjuvanted virions by either route completely eliminated viral shedding after challenge with live virus and the GMCSF vaccine reduced the number of birds shedding virus.
机译:灭活的病毒疫苗通常会产生次优的免疫反应。将佐剂掺入疫苗中以增加其免疫原性,但是目前可用的佐剂具有缺点,限制了它们在人和兽医学中的使用。这需要开发新的佐剂和递送系统。细胞因子已经作为疫苗中的佐剂进行了广泛的测试,但是遇到了诸如从抗原扩散,半衰期短和生产成本等挑战。为了解决这个问题,我们开发了一种技术,该技术可有效生产带有膜结合细胞因子的灭活的全病毒流感疫苗。将细胞因子束缚在目标抗原上可使免疫调节剂与抗原保持紧密接触,从而确保由佐剂募集或激活的免疫细胞也与抗原反应。流感可用于测试此模型,因为其表面蛋白HA和NA包含保守的信号序列,这些信号序列将这些蛋白引导到受感染的细胞表面,然后由萌芽的病毒体将其拾取。将含有与这些信号序列融合的细胞因子的质粒引入MDCK细胞系,并且在表达时,将融合蛋白导向细胞膜上的脂质岛。当细胞感染流行性感冒时,新病毒会在脂质岛上聚集并将融合蛋白整合到病毒包膜中。此外,这种基于哺乳动物细胞培养的生产系统绕开了基于鸡蛋的流感疫苗生产系统中当前存在的许多局限性。该模型已在鸡模型中使用膜结合的C3d,GMCSF,IL2和IL4作为佐剂进行了测试。皮下注射的GMCSF佐剂疫苗和皮下和鼻内注射的C3d佐剂疫苗产生的抗体效价明显高于单独接种灭活病毒的抗体效价。通过任一种途径的C3d辅助病毒体疫苗接种,都可以完全消除活病毒攻击后的病毒脱落,而GMCSF疫苗减少了鸟类脱落病毒的数量。

著录项

  • 作者

    Fischer, David D.;

  • 作者单位

    Wayne State University.;

  • 授予单位 Wayne State University.;
  • 学科 Biology Cell.;Health Sciences Immunology.;Biology Virology.;Biology Microbiology.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 135 p.
  • 总页数 135
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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