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Marieke A. D. van Zoelen

Researcher at University of Amsterdam

Publications -  30
Citations -  3190

Marieke A. D. van Zoelen is an academic researcher from University of Amsterdam. The author has contributed to research in topics: Inflammation & Sepsis. The author has an hindex of 22, co-authored 30 publications receiving 2880 citations. Previous affiliations of Marieke A. D. van Zoelen include University of Michigan.

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Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock

TL;DR: It is demonstrated that mice lacking Mrp8-Mrp14 complexes are protected from endotoxin-induced lethal shock and Escherichia coli–induced abdominal sepsis, indicating new inflammatory components that amplify phagocyte activation during sepsi upstream of TNFα–dependent effects.
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Role of toll-like receptors 2 and 4, and the receptor for advanced glycation end products in high-mobility group box 1-induced inflammation in vivo

TL;DR: Data indicate that HMGB-1 induces release of cytokines, activation of coagulation, and neutrophil recruitment in vivo via a mechanism that at least in part depends on TLR-4 and RAGE.
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Induction of IRAK-M Is Associated with Lipopolysaccharide Tolerance in a Human Endotoxemia Model

TL;DR: Analysis of expression kinetics of MyD88short, IL-1R-associated kinase (IRAK)-1, IRAK-M, ST2, suppressor of cytokine signaling-1 and -3, SHIP-1, and MAP kinase phosphatase-1 expression indicated that the observed LPS tolerance was associated with decreased IRAK -1 and elevated IRAk-M expression in this human model.
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Proinflammatory S100A12 Can Activate Human Monocytes via Toll-like Receptor 4

TL;DR: Human S100A12 is an endogenous TLR4 ligand that induces monocyte activation, thereby acting as an amplifier of innate immunity during early inflammation and the development of sepsis.
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Myeloid-related protein-14 contributes to protective immunity in gram-negative pneumonia derived sepsis

TL;DR: The role of MRP8/14 is identified as key player in protective innate immunity during Klebsiella pneumonia using an established model characterized by gradual growth of bacteria with subsequent dissemination.