Nanoimmunotherapy to treat ischaemic heart disease.
Animals
Anti-Inflammatory Agents
/ therapeutic use
Atherosclerosis
/ diagnosis
Humans
Immunity, Innate
/ drug effects
Immunotherapy
/ methods
Inflammation Mediators
/ antagonists & inhibitors
Molecular Targeted Therapy
Myocardial Ischemia
/ diagnosis
Nanomedicine
/ methods
Signal Transduction
/ drug effects
Journal
Nature reviews. Cardiology
ISSN: 1759-5010
Titre abrégé: Nat Rev Cardiol
Pays: England
ID NLM: 101500075
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
pubmed:
14
9
2018
medline:
12
11
2019
entrez:
14
9
2018
Statut:
ppublish
Résumé
Atherosclerosis is a chronic disease of the large arteries and the underlying cause of myocardial infarction and stroke. Atherosclerosis is driven by cholesterol accumulation and subsequent inflammation in the vessel wall. Despite the clinical successes of lipid-lowering treatments, atherosclerosis remains one of the major threats to human health worldwide. Over the past 20 years, insights into cardiovascular immunopathology have provided a plethora of new potential therapeutic targets to reduce the risk of atherosclerosis and have shifted the therapeutic focus from lipids to inflammation. In 2017, the CANTOS trial demonstrated for the first time the beneficial effects of targeting inflammation to treat cardiovascular disease by showing that IL-1β inhibition can reduce the recurrence rate of cardiovascular events in a large cohort of patients. At the same time, preclinical studies have highlighted nanotechnology approaches that facilitate the specific targeting of innate immune cells, which could potentially generate more effective immunomodulatory treatments to induce disease regression and prevent the recurrence of cardiovascular events. The clinical translation of such nanoimmunotherapies and their application to treat patients with ischaemic heart disease are challenges that lie ahead.
Identifiants
pubmed: 30209355
doi: 10.1038/s41569-018-0073-1
pii: 10.1038/s41569-018-0073-1
pmc: PMC10621601
mid: NIHMS1939975
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Inflammation Mediators
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
21-32Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL125703
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL144072
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL131478
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB009638
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL118440
Pays : United States
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