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PANDORA SIGNED

Pandemics Outbreaks Rationalized: towards a universal therapy to eliminate intracellular pathogens and drug resistance

Total Cost €

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EC-Contrib. €

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Partnership

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 PANDORA project word cloud

Explore the words cloud of the PANDORA project. It provides you a very rough idea of what is the project "PANDORA" about.

recognising    model    combine    nanocarriers    super    infectious    nanoparticles    selective    antimicrobial    cells    binding    reversely    membrane    polymersomes    repertoire    bar    designed    probe    fusion    bind    inspired    sequence    agent    human    eradicate    phagocytosis    chase    immunity    pandora    intracellular    car    reproduce    clearance    drug    caused    selectively    vision    mycobacteriophages    eradicating    antibodies    abs    proteasome    bacterial    combined    leaving    autolisins    universal    recognise    molecular    polymeric    diseases    infected    untouched    resistance    pillars    invented    mycobacterial    pandemics    receptor    revolution    tuberculosis    infection    engineer    antigen    attack    mycobacteria    codes    payload    proteins    wall    worst    first    macrophage    counteract    cure    effector    pathogens    chimeric    bacteriophages    organism    carry    either    fight    completely    create    species    therapy    complete    locally    revolutionise    causing    nature    core    ubiquitin    memory    circulating    region    express    ab    infections    expressed    triggered    ligands    eradication   

Project "PANDORA" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA 

Organization address
address: CARRER BALDIRI REIXAC PLANTA 2A 10-12
city: BARCELONA
postcode: 8028
website: http://www.ibecbarcelona.eu

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Spain [ES]
 Total cost 1˙495˙018 €
 EC max contribution 1˙495˙018 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2020
 Duration (year-month-day) from 2020-08-01   to  2025-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA ES (BARCELONA) coordinator 1˙495˙018.00

Map

 Project objective

I propose here a research vision that aims to revolutionise the way we cure infections caused by intracellular pathogens, with the aim to find a universal therapy to infectious diseases that will also counteract the development of drug resistance. In PANDORA, I will specifically focus on eradicating human tuberculosis, one of the worst pandemics so far. To do this, I will first probe what are the molecular ‘bar-codes’ of infected cells, namely those specific membrane proteins that cells express upon infection. I will use this to reversely engineer a repertoire of super-selective polymeric nanoparticles - known as Polymersomes - that will carry ligands to recognise, bind, and selectively attack infected cells only, while leaving non-infected cells completely untouched. Such nanocarriers will access the infected cells and locally deliver their payload, which is the core technology of the therapy. Such technology will be inspired by what nature invented: I will reproduce the binding sequence of autolisins, proteins expressed by bacteriophages that specifically bind the wall of Mycobacteria species (the agent causing tuberculosis). I will thus create fusion antibodies (Ab) characterized by (i) the binding sequence of mycobacteriophages autolisins (for selective recognising intracellular Mycobacterial wall) and (ii) an effector region promoting bacterial clearance through either the macrophage-triggered phagocytosis or an ubiquitin-proteasome system. This therapy will represent a complete revolution in the field of new antimicrobial development, as it will combine complete bacterial eradication, development of memory immunity and fight against drug resistance, the three core pillars of this project. The super-selective polymersomes carrying the Abs-based universal therapy will be combined with the development of chimeric antigen receptor T-cells (CAR-T) against infection. These T-cells will be designed to chase and eradicate circulating infected cells in model organism.

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The information about "PANDORA" are provided by the European Opendata Portal: CORDIS opendata.

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