• DocumentCode
    2376710
  • Title

    Biomimetic approaches to modulating the T cell immune response with nano- and micro- particles

  • Author

    Demento, Stacey ; Steenblock, Erin R. ; Fahmy, Tarek M.

  • Author_Institution
    Dept. of Biomed. Eng., Yale Univ., New Haven, CT, USA
  • fYear
    2009
  • fDate
    3-6 Sept. 2009
  • Firstpage
    1161
  • Lastpage
    1166
  • Abstract
    Modulating immune responses to pathogen invasion and even tumors is a major goal in immunotherapy. T cells play a central role in these responses. Progress towards that goal is accomplished by stimulating the antigen-specific T cell immune response in vivo through active immunization, or by re-transfer of large numbers of T cells expanded outside the body in a process called adoptive immunotherapy. In both vaccination and adoptive cellular therapy, there is a critical need for a reliable and effective antigen-presentation strategy that stimulates T cells in a specific and efficient manner. Biodegradable nanoparticles can be engineered with bacterial lipopolysaccharides coating thus priming dendritic cells for improved immunization. Alternatively, micron-sized particles can be made to approximate the natural ability of dendritic cells in stimulating T cells by surface modification with the appropriate T cell antigens. Here we show how both of these approaches can be employed to produce safe and effective vaccine and cellular therapeutics.
  • Keywords
    biodegradable materials; biomimetics; cellular biophysics; diseases; microorganisms; nanobiotechnology; nanoparticles; patient treatment; active immunization; adoptive cellular therapy; antigen-presentation strategy; antigen-specific T cell immune response; bacterial lipopolysaccharides coating; biodegradable nanoparticles; dendritic cells; immunotherapy; in vivo study; microparticles; pathogen invasion; tumors; vaccination; vaccine therapeutics; Animals; Antigen Presentation; Antigens, Viral; Biocompatible Materials; Biomedical Engineering; Biomimetic Materials; Capsules; Dendritic Cells; Epitopes, T-Lymphocyte; Female; Immunotherapy, Adoptive; Mice; Mice, Inbred C57BL; Nanocapsules; Ovalbumin; T-Lymphocytes; West Nile virus;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
  • Conference_Location
    Minneapolis, MN
  • ISSN
    1557-170X
  • Print_ISBN
    978-1-4244-3296-7
  • Electronic_ISBN
    1557-170X
  • Type

    conf

  • DOI
    10.1109/IEMBS.2009.5332625
  • Filename
    5332625