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  1. Article ; Online: N-Acetyl Galactosamine Targeting: Paving the Way for Clinical Application of Nucleotide Medicines in Cardiovascular Diseases.

    Biessen, Erik A L / Van Berkel, Theo J C

    Arteriosclerosis, thrombosis, and vascular biology

    2021  Volume 41, Issue 12, Page(s) 2855–2865

    Abstract: While the promise of oligonucleotide therapeutics, such as (chemically modified) ASO (antisense oligonucleotides) and short interfering RNAs, is undisputed from their introduction onwards, their unfavorable pharmacokinetics and intrinsic capacity to ... ...

    Abstract While the promise of oligonucleotide therapeutics, such as (chemically modified) ASO (antisense oligonucleotides) and short interfering RNAs, is undisputed from their introduction onwards, their unfavorable pharmacokinetics and intrinsic capacity to mobilize innate immune responses, were limiting widespread clinical use. However, these major setbacks have been tackled by breakthroughs in chemistry, stability and delivery. When aiming an intervention hepatic targets, such as lipid and sugar metabolism, coagulation, not to mention cancer and virus infection, introduction of N-acetylgalactosamine aided targeting technology has advanced the field profoundly and by now a dozen of N-acetylgalactosamine therapeutics for these indications have been approved for clinical use or have progressed to clinical trial stage 2 to 3 testing. This technology, in combination with major advances in oligonucleotide stability allows safe and durable intervention in targets that were previously deemed undruggable, such as Lp(a) and PCSK9 (proprotein convertase subtilisin/kexin type 9), at high efficacy and specificity, often with as little as 2 doses per year. Their successful use even the most visionary would not have predicted 2 decades ago. Here, we will review the evolution of N-acetylgalactosamine technology. We shall outline their fundamental design principles and merits, and their application for the delivery of oligonucleotide therapeutics to the liver. Finally, we will discuss the perspectives of N-acetylgalactosamine technology and propose directions for future research in receptor targeted delivery of these gene medicines.
    MeSH term(s) Acetylgalactosamine/chemistry ; Cardiovascular Diseases/drug therapy ; Drug Delivery Systems ; Genetic Therapy/methods ; Hepatocytes/drug effects ; Hepatocytes/metabolism ; Humans ; Liver/drug effects ; Liver/metabolism ; Oligonucleotides/administration & dosage ; RNAi Therapeutics
    Chemical Substances Oligonucleotides ; Acetylgalactosamine (KM15WK8O5T)
    Language English
    Publishing date 2021-10-14
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1221433-4
    ISSN 1524-4636 ; 1079-5642
    ISSN (online) 1524-4636
    ISSN 1079-5642
    DOI 10.1161/ATVBAHA.121.316290
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Arterial lymphangiogenesis ReSPONDINg 2 a new cue: the R-spondin2/LRG4 axis limits VEGFR3-mediated lymphangiogenesis and reverse cholesterol transport.

    Sluimer, Judith C / Biessen, Erik A L

    Cardiovascular research

    2021  Volume 117, Issue 6, Page(s) 1417–1419

    MeSH term(s) Cholesterol ; Cues ; Lymphangiogenesis ; Vascular Endothelial Growth Factor Receptor-3
    Chemical Substances Cholesterol (97C5T2UQ7J) ; Vascular Endothelial Growth Factor Receptor-3 (EC 2.7.10.1)
    Language English
    Publishing date 2021-03-12
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 80340-6
    ISSN 1755-3245 ; 0008-6363
    ISSN (online) 1755-3245
    ISSN 0008-6363
    DOI 10.1093/cvr/cvab050
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Monocyte heterogeneity in cardiovascular disease.

    Ruder, Adele V / Wetzels, Suzan M W / Temmerman, Lieve / Biessen, Erik A L / Goossens, Pieter

    Cardiovascular research

    2023  Volume 119, Issue 11, Page(s) 2033–2045

    Abstract: Monocytes circulate the vasculature at steady state and are recruited to sites of inflammation where they differentiate into macrophages (MФ) to replenish tissue-resident MФ populations and engage in the development of cardiovascular disease (CVD). ... ...

    Abstract Monocytes circulate the vasculature at steady state and are recruited to sites of inflammation where they differentiate into macrophages (MФ) to replenish tissue-resident MФ populations and engage in the development of cardiovascular disease (CVD). Monocytes display considerable heterogeneity, currently reflected by a nomenclature based on their expression of cluster of differentiation (CD) 14 and CD16, distinguishing CD14++CD16- classical (cMo), CD14++CD16+ intermediate (intMo) and CD14+CD16++ non-classical (ncMo) monocytes. Several reports point to shifted subset distributions in the context of CVD, with significant association of intMo numbers with atherosclerosis, myocardial infarction, and heart failure. However, clear indications of their causal involvement as well as their predictive value for CVD are lacking. As recent high-parameter cytometry and single-cell RNA sequencing (scRNA-Seq) studies suggest an even higher degree of heterogeneity, better understanding of the functionalities of these subsets is pivotal. Considering their high heterogeneity, surprisingly little is known about functional differences between MФ originating from monocytes belonging to different subsets, and implications thereof for CVD pathogenesis. This paper provides an overview of recent findings on monocyte heterogeneity in the context of homeostasis and disease as well as functional differences between the subsets and their potential to differentiate into MФ, focusing on their role in vessels and the heart. The emerging paradigm of monocyte heterogeneity transcending the current tripartite subset division argues for an updated nomenclature and functional studies to substantiate marker-based subdivision and to clarify subset-specific implications for CVD.
    MeSH term(s) Humans ; Monocytes/metabolism ; Cardiovascular Diseases/diagnosis ; Cardiovascular Diseases/metabolism ; Macrophages/metabolism ; Atherosclerosis/metabolism ; Myocardial Infarction/metabolism ; Receptors, IgG/metabolism ; Lipopolysaccharide Receptors
    Chemical Substances Receptors, IgG ; Lipopolysaccharide Receptors
    Language English
    Publishing date 2023-05-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80340-6
    ISSN 1755-3245 ; 0008-6363
    ISSN (online) 1755-3245
    ISSN 0008-6363
    DOI 10.1093/cvr/cvad069
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Culture density influences the functional phenotype of human macrophages.

    Ruder, Adele V / Temmerman, Lieve / van Dommelen, Joep M A / Nagenborg, Jan / Lu, Chang / Sluimer, Judith C / Goossens, Pieter / Biessen, Erik A L

    Frontiers in immunology

    2023  Volume 14, Page(s) 1078591

    Abstract: Macrophages (MΦ) are commonly ... ...

    Abstract Macrophages (MΦ) are commonly cultured
    MeSH term(s) Humans ; Inflammasomes/metabolism ; Macrophages/metabolism ; Cytokines/metabolism ; Phenotype ; Lipids
    Chemical Substances Inflammasomes ; Cytokines ; Lipids
    Language English
    Publishing date 2023-03-10
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1078591
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Macrophage complexity in human atherosclerosis: opportunities for treatment?

    Biessen, Erik A L / Wouters, Kristiaan

    Current opinion in lipidology

    2017  Volume 28, Issue 5, Page(s) 419–426

    Abstract: Purpose of review: The pivotal role of macrophages in experimental atherosclerosis is firmly established, but their contribution to human disease is less well defined. In this review we have outlined the current insights on macrophage phenotypes and ... ...

    Abstract Purpose of review: The pivotal role of macrophages in experimental atherosclerosis is firmly established, but their contribution to human disease is less well defined. In this review we have outlined the current insights on macrophage phenotypes and their presumed precursors, monocytes, in clinical atherosclerosis, and their association with disease progression. Moreover, we will assess major clinical modifiers of macrophage-mediated plaque inflammation and define the outstanding questions for further study.
    Recent findings: Our survey indicates that macrophage accumulation and status in human plaques are linked with lesion progression and destabilization as well as with symptomatic coronary artery disease. Likewise, levels of their precursors, circulating monocytes were repeatedly seen to associate with atherosclerosis and to predict clinical outcome. Furthermore, the presence and phenotype of both macrophages and monocytes appears to be responsive to the traditional risk factors of atherosclerosis, including hypercholesterolemia, hypertension, and type 2 diabetes, and to treatment thereof, with clear repercussions on disease development.
    Summary: Although plaque macrophages and their precursor cells do represent attractive targets for treating cardiovascular diseases, this therapeutic avenue requires much deeper understanding of the complexity of macrophage biology in human atherosclerosis than available at present.
    Language English
    Publishing date 2017-10
    Publishing country England
    Document type Journal Article
    ZDB-ID 1045394-5
    ISSN 1473-6535 ; 0957-9672
    ISSN (online) 1473-6535
    ISSN 0957-9672
    DOI 10.1097/MOL.0000000000000447
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Protocol for multispectral imaging on cryosections to map myeloid cell heterogeneity in its spatial context.

    Wieland, Elias B / Kempen, Laura J A P / Lu, Chang / Donners, Marjo M P C / Biessen, Erik A L / Goossens, Pieter

    STAR protocols

    2023  Volume 4, Issue 4, Page(s) 102601

    Abstract: Recent technical advances, such as single-cell RNA sequencing and mass cytometry, improve identification of cell types and subsets in a range of healthy and diseased tissues at the expense of their cellular and molecular context. Here, we present a ... ...

    Abstract Recent technical advances, such as single-cell RNA sequencing and mass cytometry, improve identification of cell types and subsets in a range of healthy and diseased tissues at the expense of their cellular and molecular context. Here, we present a protocol for in situ multispectral imaging to map myeloid cell heterogeneity in tissue cryosections, describing steps for cutting sequential sections, antibody titration, and building a spectral library. We then detail procedures for multispectral imaging and preparing data for downstream analysis. For complete details on the use and execution of this protocol, please refer to Goossens et al. (2022).
    MeSH term(s) Myeloid Cells ; Cryoultramicrotomy ; Diagnostic Imaging ; Gene Library
    Language English
    Publishing date 2023-09-23
    Publishing country United States
    Document type Journal Article
    ISSN 2666-1667
    ISSN (online) 2666-1667
    DOI 10.1016/j.xpro.2023.102601
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Unwrapped and uNCORked: PPAR-γ repression in atherosclerosis.

    Van der Vorst, Emiel P C / Biessen, Erik A L

    European heart journal

    2019  Volume 43, Issue 7, Page(s) e32–e34

    Language English
    Publishing date 2019-11-21
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 603098-1
    ISSN 1522-9645 ; 0195-668X
    ISSN (online) 1522-9645
    ISSN 0195-668X
    DOI 10.1093/eurheartj/ehz770
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: SCRIBbling the role of endothelial polarity in atherosclerosis.

    Donners, Marjo M P C / Biessen, Erik A L

    Cardiovascular research

    2019  Volume 115, Issue 14, Page(s) 1937–1939

    MeSH term(s) Animals ; Atherosclerosis ; Mice
    Language English
    Publishing date 2019-07-03
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 80340-6
    ISSN 1755-3245 ; 0008-6363
    ISSN (online) 1755-3245
    ISSN 0008-6363
    DOI 10.1093/cvr/cvz171
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Book ; Online ; Thesis: Uremia-induced effects on cardioregulatory mechanisms in the context of the cardiorenal syndrome

    Wollenhaupt, Julia [Verfasser] / Jankowski, Joachim [Akademischer Betreuer] / Blank, Lars Mathias [Akademischer Betreuer] / Biessen, Erik A. L. [Akademischer Betreuer]

    2023  

    Author's details Julia Wollenhaupt ; Joachim Jankowski, Lars M. Blank, Erik A. L. Biessen
    Keywords Biowissenschaften, Biologie ; Life Science, Biology
    Subject code sg570
    Language English
    Publisher Universitätsbibliothek der RWTH Aachen
    Publishing place Aachen
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  10. Article ; Online: Transcriptional Sex Dimorphism in Human Atherosclerosis Relates to Plaque Type.

    Jin, Han / Mees, Barend M E / Biessen, Erik A L / Sluimer, Judith C

    Circulation research

    2021  Volume 129, Issue 12, Page(s) 1175–1177

    MeSH term(s) Atherosclerosis/genetics ; Atherosclerosis/metabolism ; Atherosclerosis/pathology ; Female ; Humans ; Male ; Plaque, Atherosclerotic/genetics ; Plaque, Atherosclerotic/metabolism ; Sex ; Transcriptome
    Language English
    Publishing date 2021-10-18
    Publishing country United States
    Document type Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 80100-8
    ISSN 1524-4571 ; 0009-7330 ; 0931-6876
    ISSN (online) 1524-4571
    ISSN 0009-7330 ; 0931-6876
    DOI 10.1161/CIRCRESAHA.121.320099
    Database MEDical Literature Analysis and Retrieval System OnLINE

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