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Alan Aderem

Researcher at Seattle Children's Research Institute

Publications -  248
Citations -  50351

Alan Aderem is an academic researcher from Seattle Children's Research Institute. The author has contributed to research in topics: Innate immune system & Immune system. The author has an hindex of 99, co-authored 246 publications receiving 46682 citations. Previous affiliations of Alan Aderem include University of Cape Town & Fred Hutchinson Cancer Research Center.

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The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5.

TL;DR: It is reported that mammalian TLR5 recognizes bacterial flagellin from both Gram-positive and Gram-negative bacteria, and that activation of the receptor mobilizes the nuclear factor NF-κB and stimulates tumour necrosis factor-α production, and the data suggest thatTLR5, a member of the evolutionarily conserved Toll-like receptor family, has evolved to permit mammals specifically to detect flageLLated bacterial pathogens.
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Toll-like receptors in the induction of the innate immune response

TL;DR: A group of proteins that comprise the Toll or Toll-like family of receptors perform this role in vertebrate and invertebrate organisms and it is therefore not surprising that studies of the mechanism by which they act has revealed new and important insights into host defence.
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Mechanisms of phagocytosis in macrophages

TL;DR: Macrophages also play an important role in the recognition and clearance of apoptotic cells; a notable feature of this process is the absence of an inflammatory response.
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The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between Toll-like receptors

TL;DR: The data suggest that TLRs sample the contents of the phagosome independent of the nature of the contents, and can establish a combinatorial repertoire to discriminate among the large number of pathogen-associated molecular patterns found in nature.
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Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron.

TL;DR: This finding represents a new component of the innate immune system and the acute phase response to infection and limits bacterial growth by sequestrating the iron-laden siderophore.