Pin1-Targeted Therapy for Systemic Lupus Erythematosus.

ABSTRACT:

Objective

Systemic lupus erythematosus (SLE) is a debilitating autoimmune disease affecting multiple organs in the body, but therapeutic options are still very limited and often come with adverse effects. Increasing evidence has underlined an important role of the Toll-like receptor 7 (TLR-7)/TLR-9/interleukin-1 receptor-associated kinase 1 (IRAK-1)/interferon regulatory factor 7 (IRF-7) pathway in the development and progression of SLE. Notably, the prolyl isomerase Pin1 is an essential regulator of IRAK-1 in TLR-7/TLR-9 signaling, but its role in SLE is unknown. We undertook this study to determine whether Pin1 is activated and plays any role in the development and treatment of SLE.

Methods

Activation of Pin1 and TLR-7/TLR-9/IRAK-1/IRF-7 signaling was determined in various

SUBMITTER: Wei S 

PROVIDER: S-EPMC5493308 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature