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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. €

0

Partnership

0

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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.

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

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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