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@INBOOK{Hashkes:280929,
author = {Saavedra, Victor and Moghaddas, Fiona and Latz, Eicke and
Masters, Seth L.},
editor = {Hashkes, Philip J. and Laxer, Ronald M. and Simon, Anna},
title = {{P}attern {R}ecognition {R}eceptors in {A}utoinflammation},
address = {Cham},
publisher = {Springer International Publishing},
reportid = {DZNE-2025-01012},
pages = {61 - 87},
year = {2019},
comment = {Textbook of Autoinflammation / Hashkes, Philip J. (Editor)
; Cham : Springer International Publishing, 2019, Chapter 4
; ISBN: 978-3-319-98604-3 ; doi:10.1007/978-3-319-98605-0},
booktitle = {Textbook of Autoinflammation /
Hashkes, Philip J. (Editor) ; Cham :
Springer International Publishing,
2019, Chapter 4 ; ISBN:
978-3-319-98604-3 ;
doi:10.1007/978-3-319-98605-0},
abstract = {The immune system is essential for maintenance of tissue
homeostasis. This task requires that immune cells detect and
respond to dyshomeostatic states (when homeostasis has
broken down) that can occur during invasion of the host with
pathogenic microbes, after sterile trauma of tissues or
during metabolic derangements. Research in the field of
innate immunity has uncovered many molecular mechanisms by
which the immune system can prevent the spread of infection,
restore damaged tissues and respond to altered metabolism.
These pathways involve different classes of pattern
recognition receptors, some of which can directly detect
minimal motifs (patterns) that are common to multiple
pathogens or types of damaged cells. Here, we summarize the
general concepts that have been developed to explain how
immune recognition of dyshomeostasis is achieved and discuss
our current knowledge of the innate immune signaling
receptors that are known to directly bind ligands.},
cin = {AG Latz},
cid = {I:(DE-2719)1013024},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)7},
doi = {10.1007/978-3-319-98605-0_4},
url = {https://pub.dzne.de/record/280929},
}