Intracellular Carrier Against Resistant microOrganisms (ICARO)

Grant number: 101046927

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Key facts

  • Disease

    Disease X
  • Start & end year

    2022
    2026
  • Known Financial Commitments (USD)

    $3,326,722.17
  • Funder

    European Commission
  • Principal Investigator

    Hernandez Alberto
  • Research Location

    Spain
  • Lead Research Institution

    ARRAYS-FOR-CELL NANODEVICES SL
  • Research Priority Alignment

    N/A
  • Research Category

    Vaccines research, development and implementation

  • Research Subcategory

    Vaccine design and administration

  • Special Interest Tags

    Innovation

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Vaccines have a history of success in the control of infectious diseases. The need for new efficient vaccination strategies is of particular significance due to the emergence of new pathogens, lack of effective antivirals and the growing scenario of antibiotic resistances. Intracellular pathogens and viruses are responsible for epidemics like tuberculosis, malaria, or COVID-19. CD8+ T cells eliminate cells exposing antigens derived from intracellular pathogens via Major-Histocompatibility Complex class I (MHC-I). This antigen-presentation pathway is often subverted by viruses or intravacuolar pathogens, for which the antigenic repertoire is greatly diminished. ICARO take advantage of MEMS capabilities to obtain the proof-of-concept for a new generation of vaccines needed for diseases caused by intracellular pathogens (viruses, bacteria and protozoa) with a high societal impact. The biochips technology underlying this project has been already proven: biochips are optimal to reach and work in the intracellular environment: volume in the range of μm3, easy to manipulate, proven internalization by phagocytic and non-phagocytic cells and the ability to remain long period of time in the cytosol. Our vision is to develop silicon microchips that will cross the cellular barriers carrying whole inactivated pathogens to the cytosol for its presentation by MHC-I. By achieving that, ICARO might be a groundbreaking new vaccination strategy to boost CD8+ T cells responses by a rapid scouting of a full repertoire of antigens for a given inactivated pathogen. We aim to develop standardized methods for ICARO manufacturing and functionalisation to be easily applicable to other pathogens, thus accelerating the generation of new vaccines in the future