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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.

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

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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