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PAMpeR SIGNED

Patroller monocytes as modulators of diabetic retinopathy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 PAMpeR project word cloud

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

trophic    preceded    lower    dm    protective    nonproliferative    investigation    preferentially    variance    profile    monocyte    damage    data    classic    adults    capture    diabetes    indicate    period    patroller    incorporate    suggested    endothelium    t1dm    subjects    protect    magnitude    active    vascular    preliminary    enabled    patients    biosynthetic    discrete    applicability    repairing    first    actions    speed    relation    healing    healthy    delivered    time    efficacy    setting    transcriptional    blindness    circulating    seek    leukostasis    dr    activates    functional    diabetic    inflammatory    latency    monocytes    repair    losing    complement    protecting    complication    mimic    vessels    clinical    subpopulation    types    cells    cytokines    rolling    human    compare    endogenous    initial    subset    patrollers    beneficial    crawling    months    leverage    fact    retinopathy    natural    start    suggest    housekeeping    molecular    adapt    expectation    patrol    contrast    retinal    history   

Project "PAMpeR" data sheet

The following table provides information about the project.

Coordinator
OSPEDALE SAN RAFFAELE SRL 

Organization address
address: VIA OLGETTINA 60
city: MILANO
postcode: 20132
website: www.hsr.it

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 Italy [IT]
 Total cost 180˙277 €
 EC max contribution 180˙277 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2018
 Duration (year-month-day) from 2018-05-16   to  2020-05-15

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    OSPEDALE SAN RAFFAELE SRL IT (MILANO) coordinator 180˙277.00

Map

 Project objective

'Diabetic retinopathy is the first vascular complication of diabetes and the leading cause of legal blindness among adults in Europe. The fact that diabetic retinopathy is preceded by a long latency period has suggested to us that its natural history could incorporate a phase of vascular repair, active after short duration of diabetes and eventually losing efficacy over time. “Patroller” monocytes, a discrete subpopulation of circulating monocytes, patrol healthy vessels by “crawling” on the endothelium at a speed that is order of magnitude lower than rolling, and at variance with the 'classic' monocyte subset produce preferentially housekeeping and trophic factors rather than inflammatory cytokines. Our preliminary data strongly support a role of patrollers, in protecting and repairing retinal vessels in diabetes; suggest that the beneficial activities are delivered during leukostasis; and indicate that 5 months of diabetes duration activates a healing/protective transcriptional program in patrollers.

I seek to learn whether the biosynthetic profile of patrollers changes in relation to increasing duration of diabetes and evolving retinal vascular damage; and, most importantly, I seek to bring the study of patrollers to clinical investigation.

The Objectives are to: 1. Learn if circulating patrollers adapt their biosynthetic profile to different diabetes duration (3 and 9 months) and to the evolving vascular damage 2. Bring the project to clinical applicability by start setting up a human study that aims to compare and contrast the number of circulating patrollers, as well as selected biosynthetic and functional characteristics of these cells, in T1DM patients with no DR after 4-8 years of DM, in T1DM patients with initial nonproliferative DR, and in healthy control subjects.

The expectation is to capture from endogenous systems the types of molecular actions that protect the vessels in early diabetes; and thus be enabled to mimic, complement, or leverage'

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

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