Intracellular Carrier Against Resistant microOrganisms (ICARO)
- Funded by European Commission
- Total publications:0 publications
Grant number: 101046927
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Key facts
Disease
Disease XStart & end year
20222026Known Financial Commitments (USD)
$3,326,722.17Funder
European CommissionPrincipal Investigator
Hernandez AlbertoResearch Location
SpainLead Research Institution
ARRAYS-FOR-CELL NANODEVICES SLResearch 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