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Targeting epigenetic REPROGRamming of innate immune cells in Atherosclerosis Management and other chronic inflammatory diseases

Project
Up to 70% of cardiovascular events are not prevented by current therapeutic regimens. In search for additional, innovative strategies, immune cells have been recognized as key players contributing to atherosclerotic plaque progression and destabilization. Particularly the role of innate immune cells is of major interest, following the recent paradigm shift that innate immunity, considered to be incapable of learning ability, does exhibit a memory feature transduced via epigenetic modulation. Compelling evidence shows that atherosclerotic factors promote immune cell migration by pre-activation of innate immune cells. In this project called REPROGRAM, we aim to prove that innate immune cell activation via epigenetic reprogramming perpetuates the upheld systemic inflammatory state in cardiovascular disease which is common in other chronic inflammatory diseases. This opens a new therapeutic area in which epigenetic modulation of innate immune cells effectively decreases systemic inflammation impacting on chronic inflammation as well as the development of co-morbidities. The integrated use of in vitro, ex vivo and in vivo studies, including cells, mice and patients, allows translation from in vitro mechanisms to diseases (molecule-to-man) and extrapolation to cohorts (man-to-mass), enabling us to demonstrate relevance and therapeutic potential of targeting trained immunity in cardiovascular and chronic inflammatory diseases. Enforced by the promising data in oncology, the future prospects for epigenetic interventions in cardiovascular and chronic inflammatory diseases are eminent, attested by the large residual cardiovascular disease burden and the huge societal impact of other chronic inflammatory diseases. The REPROGRAM consortium consisting of key opinion leaders in the field of cardiovascular (systems) biology, immunology, epigenetic therapies and rheumatoid arthritis, with a large intersectoral network, guarantees rapid translation of early mechanistic discoveries.
  • Overview
  • Publications

Overview

Departments involved

Dipartimento di Scienze Farmacologiche e Biomolecolari Rodolfo Paoletti   Principale  

Type

H20_RIA - Horizon 2020_Research & Innovation Action/Innovation Action

Funder

EUROPEAN COMMISSION
External Organization Funding Organization

Date/time interval

January 1, 2016 - December 31, 2019

Project duration

48 months

Publications

Outputs (6)

Progress and prospects of biological approaches targeting PCSK9 for cholesterol-lowering, from molecular mechanism to clinical efficacy 
EXPERT OPINION ON BIOLOGICAL THERAPY
TAYLOR & FRANCIS
2020
Academic Article
Open Access
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Lipid Lowering and Incidence of Cataract, a Role for Fibrates 
CLINICAL PHARMACOLOGY & THERAPEUTICS
NATURE PUBLISHING GROUP
2019
Academic Article
Reserved Access
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Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 
ATHEROSCLEROSIS
ELSEVIER
2018
Academic Article
Partially Open Access
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Familial hypercholesterolemia treatments : guidelines and new therapies 
ATHEROSCLEROSIS
ELSEVIER
2018
Academic Article
Reserved Access
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Reduction of low density lipoprotein-cholesterol and cardiovascular events with proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors and statins : an analysis of FOURIER, SPIRE, and the Cholesterol Treatment Trialists Collaboration 
EUROPEAN HEART JOURNAL
OXFORD UNIVERSITY PRESS
2018
Academic Article
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The Interplay of Lipids, Lipoproteins, and Immunity in Atherosclerosis 
CURRENT ATHEROSCLEROSIS REPORTS
SPRINGER
2018
Academic Article
Partially Open Access
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