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Sökning: WFRF:(Shami Annelie) > (2020-2024) > Glucocorticoid indu...

Glucocorticoid induced TNF receptor family-related protein (GITR) – A novel driver of atherosclerosis

Bosmans, Laura A. (författare)
Academic Medical Center of University of Amsterdam (AMC)
Shami, Annelie (författare)
Lund University,Lunds universitet,Kardiovaskulär forskning - translationella studier,Forskargrupper vid Lunds universitet,Cardiovascular Research - Translational Studies,Lund University Research Groups
Atzler, Dorothee (författare)
German Centre for Cardiovascular Research,Ludwig-Maximilian University of Munich
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Weber, Christian (författare)
Maastricht University Medical Centre,German Centre for Cardiovascular Research,Munich Cluster for Systems Neurology
Gonçalves, Isabel (författare)
Lund University,Lunds universitet,Kardiovaskulär forskning - translationella studier,Forskargrupper vid Lunds universitet,Cardiovascular Research - Translational Studies,Lund University Research Groups,Skåne University Hospital
Lutgens, Esther (författare)
German Centre for Cardiovascular Research,Academic Medical Center of University of Amsterdam (AMC)
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 (creator_code:org_t)
Elsevier BV, 2021
2021
Engelska.
Ingår i: Vascular Pharmacology. - : Elsevier BV. - 1537-1891. ; 139
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
Stäng  
  • Atherosclerosis is a lipid-driven, chronic inflammatory disease. In spite of efficient lipid lowering treatments, such as statins and PCSK9 inhibitors, patients, especially those with elevated inflammatory biomarkers, still have a significant residual cardiovascular disease risk. Novel drugs targeting inflammatory mediators are needed to further reduce this residual risk. Agonistic immune checkpoint proteins, including CD86, CD40L and CD40, have been shown to be drivers of atherosclerosis. Recently, glucocorticoid-induced tumour necrosis factor receptor family-related protein (GITR), a co-stimulatory immune checkpoint protein, was identified to be pivotal in cardiovascular disease. Cardiovascular patients have elevated soluble GITR plasma levels compared to healthy controls. Furthermore, in human carotid endarterectomy plaques, GITR expression was higher in plaques from symptomatic compared to asymptomatic patients and correlated with features of plaque vulnerability. Moreover, depleting GITR reduced atherosclerotic plaque development in mice. GITR-deficient monocytes and macrophages exhibited less inflammatory potential and reduced migratory capacity. In this review, we discuss GITR's effects on various immune cells, mechanisms, signalling pathways and finally GITR's potential as a novel drug target in atherosclerosis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Atherosclerosis
Costimulatory molecule
CVD
GITR
Immune checkpoint

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