» Articles » PMID: 36538077

The Star Target in SLE: IL-17

Overview
Journal Inflamm Res
Date 2022 Dec 20
PMID 36538077
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The purpose of this review is to discuss the significance of IL-17 in SLE and the potential of IL-17-targeted therapy.

Background: Systemic lupus erythematosus (SLE) is an autoimmune disease that can affect many organs and tissues throughout the body. It is characterized by overactive B and T cells and loss of immune tolerance to autoantigens. Interleukin-17 (IL-17) is a cytokine that promotes inflammation and has been implicated in the pathogenesis of several autoimmune diseases as well as inflammatory diseases. In in vitro cellular experiments in lupus susceptible mice or SLE patients, there is substantial evidence that IL-17 is a highly promising therapeutic target.

Methods: We searched papers from PubMed database using the search terms, such as interleukin-17, systemic lupus erythematosus, treatment targets, T cells, lupus nephritis, and other relevant terms.

Results: We discuss in this paper the molecular mechanisms of IL-17 expression, Th17 cell proliferation, and the relationship between IL-17 and Th17. The significance of IL-17 in SLE and the potential of IL-17-targeted therapy are further discussed in detail.

Conclusion: IL-17 has a very high potential for the development as a star target in SLE.

Citing Articles

Soluble CD72, is a T-cell activator probably via binding to CD6 in homeostasis and autoimmunity.

Eiza N, Sabag A, Kessler O, Toubi E, Vadasz Z Front Immunol. 2024; 15:1367120.

PMID: 39026665 PMC: 11254670. DOI: 10.3389/fimmu.2024.1367120.


Evidence from mendelian randomization identifies several causal relationships between primary membranous nephropathy and gut microbiota.

Wu J, Zhang J, Huang G, Zhong Y, Yang Y, Deng P Ren Fail. 2024; 46(1):2349136.

PMID: 38770992 PMC: 11110878. DOI: 10.1080/0886022X.2024.2349136.


Integrative analysis of single-cell and bulk transcriptome data reveal the significant role of macrophages in lupus nephritis.

Wei S, Shen H, Zhang Y, Liu C, Li S, Yao J Arthritis Res Ther. 2024; 26(1):84.

PMID: 38610007 PMC: 11010324. DOI: 10.1186/s13075-024-03311-y.


Response of Psoriasis with Systemic Lupus Erythematosus to Secukinumab: A Case Report and Review of the Literature.

Dai B, Bai Y, Yu H, Huang Q, Wang L Clin Cosmet Investig Dermatol. 2023; 16:3589-3594.

PMID: 38116143 PMC: 10729829. DOI: 10.2147/CCID.S440977.


Characterization of Serum Cytokine Profiles of Patients with Active Lupus Nephritis.

Rahme Z, Franco C, Cruciani C, Pettorossi F, Zaramella A, Realdon S Int J Mol Sci. 2023; 24(19).

PMID: 37834330 PMC: 10573765. DOI: 10.3390/ijms241914883.


References
1.
Lim S, Helmick C, Bao G, Hootman J, Bayakly R, Gordon C . Racial Disparities in Mortality Associated with Systemic Lupus Erythematosus - Fulton and DeKalb Counties, Georgia, 2002-2016. MMWR Morb Mortal Wkly Rep. 2019; 68(18):419-422. PMC: 6542193. DOI: 10.15585/mmwr.mm6818a4. View

2.
Fanouriakis A, Tziolos N, Bertsias G, Boumpas D . Update οn the diagnosis and management of systemic lupus erythematosus. Ann Rheum Dis. 2020; 80(1):14-25. DOI: 10.1136/annrheumdis-2020-218272. View

3.
Park H, Li Z, Yang X, Chang S, Nurieva R, Wang Y . A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17. Nat Immunol. 2005; 6(11):1133-41. PMC: 1618871. DOI: 10.1038/ni1261. View

4.
Harrington L, Hatton R, Mangan P, Turner H, Murphy T, Murphy K . Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages. Nat Immunol. 2005; 6(11):1123-32. DOI: 10.1038/ni1254. View

5.
Miossec P, Kolls J . Targeting IL-17 and TH17 cells in chronic inflammation. Nat Rev Drug Discov. 2012; 11(10):763-76. DOI: 10.1038/nrd3794. View