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. 2017 Jul 19;18(8):826-831.
doi: 10.1038/ni.3790.

A guiding map for inflammation

Affiliations

A guiding map for inflammation

Mihai G Netea et al. Nat Immunol. .

Erratum in

  • Author Correction: A guiding map for inflammation.
    Netea MG, Balkwill F, Chonchol M, Cominelli F, Donath MY, Giamarellos-Bourboulis EJ, Golenbock D, Gresnigt MS, Heneka MT, Hoffman HM, Hotchkiss R, Joosten LAB, Kastner DL, Korte M, Latz E, Libby P, Mandrup-Poulsen T, Mantovani A, Mills KHG, Nowak KL, O'Neill LA, Pickkers P, van der Poll T, Ridker PM, Schalkwijk J, Schwartz DA, Siegmund B, Steer CJ, Tilg H, van der Meer JWM, van de Veerdonk FL, Dinarello CA. Netea MG, et al. Nat Immunol. 2021 Feb;22(2):254. doi: 10.1038/s41590-020-00846-5. Nat Immunol. 2021. PMID: 33288963 No abstract available.

Abstract

Biologists, physicians and immunologists have contributed to the understanding of the cellular participants and biological pathways involved in inflammation. Here, we provide a general guide to the cellular and humoral contributors to inflammation as well as to the pathways that characterize inflammation in specific organs and tissues.

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Figures

Figure 1
Figure 1
The immunological mechanisms leading to the induction of inflammation during the first stages of host defense against invading pathogens. α1-antitrypsin (AAT), pathogen associated molecular patterns (PAMPs), antimicrobial peptides (AMPs), danger associated molecular patterns (DAMPs), membrane attack complex (MAC), reactive oxygen species (ROS), C-reactive protein (CRP), tumour necrosis factor (TNF), interferon-γ (IFN-γ), mannose binding lectin (MBL), macrophage or monocyte (Mϕ), C-C Motif Chemokine Ligand (CCL).
Figure 2
Figure 2
The regulatory mechanisms that modulate inflammation, leading to resolution after the invading pathogens have been eliminated. Transforming growth factor β (TGF-β), α1-antitrypsin (AAT), interleukin-1 receptor antagonist (IL-1Ra), interleukin-1 receptor type I (IL-1R1), interleukin-1 receptor type II (IL-1R2) tumour necrosis factor (TNF), soluble TNF receptor (sTNFR), TNF receptor type I/II (TNFR I/II), prostaglandin E2(PGE2), interferon-γ (IFN-γ), macrophage or monocyte (Mϕ)

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