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Cited by 1,026

The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.

Programmed cell death as a defence against infection

Open access
Jorgensen, Ine, Rayamajhi, Manira, Miao, Edward A.·2017·Nature Reviews Immunology

Abstract

Eukaryotic cells can die from physical trauma, which results in necrosis. Alternatively, they can die through programmed cell death upon the stimulation of specific signalling pathways. In this Review, we discuss the role of different cell death pathways in innate immune defence against bacterial and viral infection: apoptosis, necroptosis, pyroptosis and NETosis. We describe the interactions that interweave different programmed cell death pathways, which create complex signalling networks that cross-guard each other in the evolutionary 'arms race' with pathogens. Finally, we describe how the resulting cell corpses — apoptotic bodies, pore-induced intracellular traps (PITs) and neutrophil extracellular traps (NETs) — promote the clearance of infection.

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Crossref · 10.1038/nri.2016.147

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Metadata

Authors
Jorgensen, I., Rayamajhi, M., & Miao, E. A.
Venue
Nature Reviews Immunology
Published
2017-01-31
Volume
17
Issue
3
Pages
151-164
ISSN
  • 1474-1733 (ISSN-L)
  • 1474-1741
OpenAlex
W2583964565
Cited by
1,026
References
37
FWCI
6.15
Type
journal article
Language
en
Open access
green

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.