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FusionPAMPs SIGNED

New generation of chimeric TLR2-NOD agonist compounds for vaccine adjuvants

Total Cost €

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EC-Contrib. €

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Partnership

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 FusionPAMPs project word cloud

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

leads    activated    recognition    compounds    toll    lipopeptides    tlr2    pamps    efficient    stimulation    pathogens    augment    almost    vaccines    transduction    salt    aluminium    new    vaccine    innate    rely    immunity    talk    cross    exposed    immune    human    vaccination    adjuvants    signal    modulators    defences    adjuvant    molecular    modalities    potent    ing    concentrations    lower    nod    attractive    activate    minimizing    direct    activation    linking    intracellular    pathogen    receptors    drives    microbial    mucosal    tlrs    prr    thereby    protective    expressed    synergistic    lipopolysaccharides    patterns    adaptive    employed    cytokines    prrs    ctls    th2    safe    nlrs    agonists    senses    cell    infection    pattern    regulate    primarily    potently    quality    microbes    turn    fragments    compound    surfaces    fusion    regard    single    cells    alum    effector    quantity    lectin    peptidoglycan    covalent    chimeric    pprs    performance   

Project "FusionPAMPs" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITEIT UTRECHT 

Organization address
address: HEIDELBERGLAAN 8
city: UTRECHT
postcode: 3584 CS
website: www.uu.nl

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 Netherlands [NL]
 Project website https://www.uu.nl/en/research/chemical-biology-and-drug-discovery
 Total cost 177˙598 €
 EC max contribution 177˙598 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-05-01   to  2019-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITEIT UTRECHT NL (UTRECHT) coordinator 177˙598.00

Map

 Project objective

New vaccine modalities need to be developed that can activate more potently the immune system, in this regard, adjuvants augment adaptive immune responses and can improve vaccine performance. Aluminium salt (alum) is the most commonly used adjuvant for human vaccination. However, it drives primarily TH2-effector responses and is not effective for vaccines that target mucosal surfaces. Thus, safe and potent adjuvants need to be developed that can increase and direct vaccine-specific immunity. Recent advances in our understanding of innate immune responses are providing opportunities to design better adjuvants. The innate immune system senses microbes through pattern-recognition receptors (PPRs), which include the Toll-like receptors (TLRs), and intracellular NOD-like receptors (NLRs) and C-type lectin-like (CTLs) receptors that are expressed by immune cells. Activation of these receptors leads to the production of cytokines that provide early defences during infection. Cytokines also regulate adaptive immunity by controlling the quantity and quality of B and T cell activation, which in turn results in protective immune responses to pathogens. Pathogen-associated molecular patterns (PAMPs) such as lipopolysaccharides, lipopeptides, and peptidoglycan fragments can activate PPRs and are attractive compounds for the development of new adjuvant. Although during microbial infection many different PRRs are activated, almost all adjuvants that are being developed rely on the stimulation of a single PRR. In this project, we propose that compound adjuvants derived by the covalent linking of two PAMPs (fusion PAMPs), for example, TLR2 and NOD agonists, will ensure that immune cells are being exposed to both, resulting in efficient cross talk of signal transduction pathways and in synergistic immune activation. If so, chimeric immune modulators (fusion PAMPs) can be employed at lower adjuvant concentrations, thereby minimizing unwanted side effects.

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

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