Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

ObjectiveTo detect the expression levels of TWEAK and CD163 in monocytes from the peripheral blood of patients with systemic lupus erythematosus (SLE) complicated with renal involvement (SLE+RI) and to explore the application value of TWEAK and CD163 in the diagnosis of SLE and SLE+RI.MethodsThe expression levels of TWEAK and CD163 in the monocytes of 70 SLE patients and the control group were determined by real-time fluorescence quantitative polymerase chain reaction (RT‒qPCR). To analyse the relationship between TWEAK/CD163 expression levels and laboratory examination and clinical manifestations in monocytes of SLE+RI patients. The sensitivity and specificity of TWEAK and CD163 for the diagnosis and differential diagnosis of SLE+RI were analysed by receiver operating characteristic (ROC) curves. Western blot experiments were used to evaluate the protein expression of TWEAK and CD163 in monocytes.ResultsThe expression levels of TWEAK and CD163 in monocytes were significantly greater in the SLE group than in the healthy control (HC) and rheumatoid arthritis (RA) groups. The expression levels of TWEAK and CD163 in monocytes from anti-double-stranded DNA antibody (anti-dsDNA)-positive patients and patients with proteinuria were respectively greater than those from anti-dsDNA-negative patients and patients without proteinuria. The expression levels of both genes were significantly lower after treatment than before treatment in the SLE+RI group ( < 0.05). The expression levels of TWEAK and CD163 in monocytes were positively correlated with the SLE activity score (SLEDAI) in the SLE+RI group. ROC curve analysis revealed that the area under the curve (AUC) of TWEAK expression was 0.869 in the SLE+RI group. The AUC of CD163 in the SLE+RI group was 0.792, the combined expression of TWEAK and CD163 was 0.842 in the SLE+RI group. TWEAK and CD163 protein expression in monocytes from patients with SLE+RI was significantly increased compared with that in controls.ConclusionThe expression levels of TWEAK and CD163 are increased in SLE patients, and the expression levels in SLE+RI patients are greater than those in SLE-RI patients. These findings are closely related to disease activity, autoantibody production and clinical symptoms and can be used as biomarkers for the diagnosis and activity of SLE+RI.

Download full-text PDF

Source
http://dx.doi.org/10.1177/09612033251371335DOI Listing

Publication Analysis

Top Keywords

tweak cd163
48
expression levels
36
cd163 monocytes
24
levels tweak
24
sle+ri group
20
expression
14
tweak
13
cd163
13
patients
12
sle+ri
11

Similar Publications

ObjectiveTo detect the expression levels of TWEAK and CD163 in monocytes from the peripheral blood of patients with systemic lupus erythematosus (SLE) complicated with renal involvement (SLE+RI) and to explore the application value of TWEAK and CD163 in the diagnosis of SLE and SLE+RI.MethodsThe expression levels of TWEAK and CD163 in the monocytes of 70 SLE patients and the control group were determined by real-time fluorescence quantitative polymerase chain reaction (RT‒qPCR). To analyse the relationship between TWEAK/CD163 expression levels and laboratory examination and clinical manifestations in monocytes of SLE+RI patients.

View Article and Find Full Text PDF

Baicalin Alleviates Piglet Immunosuppression Induced by via Promoting CD163/Tumor Necrosis Factor-like Weak Inducer of Apoptosis-Mediated Autophagy.

Biomolecules

May 2025

Wuhan Engineering and Technology Research Center of Animal Disease-Resistant Nutrition, School of Animal Science and Nutritional Engineering, Wuhan Polytechnic University, Wuhan 430023, China.

() causes vascular inflammation in piglets, resulting in vascular damage. However, the mechanism causing vascular inflammation remains unclear. Baicalin possesses an anti-inflammatory function.

View Article and Find Full Text PDF

Background: Vestibular schwannoma (VS) is an intracranial tumor arising from the Schwann cells of the vestibular nerve and is an important cause of sensorineural hearing loss (SNHL) in humans. The mechanisms underlying this SNHL are incompletely understood and currently, there are no drugs FDA approved specifically for VS. This knowledge gap significantly limits the development of effective treatments aimed at preventing, stabilizing, or reversing VS-induced SNHL.

View Article and Find Full Text PDF

The CD163/TWEAK/Fn14 axis: A potential therapeutic target for alleviating inflammatory bone loss.

J Orthop Translat

November 2024

Division of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.

Article Synopsis
  • Osteoclast (OC) over-activation due to inflammation is linked to bone loss, and the study investigates the role of the CD163/TWEAK/Fn14 signaling pathway in this process.
  • Researchers compared CD163-deficient mice to normal mice, analyzed the effects of CD163 and TWEAK levels in bone marrow, and studied the impacts of rCD163 supplementation and TWEAK/Fn14 blockade on bone mass.
  • Results showed that CD163 deficiency led to reduced bone mass and increased OC presence; targeting the CD163/TWEAK/Fn14 axis may offer a new therapy for inflammatory bone loss by influencing osteoclast activity.
View Article and Find Full Text PDF

Urinary biomarkers for active Lupus Nephritis that have survived independent validation across cohorts.

Kidney Int

December 2024

Biomedical Engineering Department, University of Houston, Houston, Texas, USA. Electronic address:

Article Synopsis
  • Many biomarkers for lupus nephritis have not been validated across different studies, but identifying urinary biomarkers that can differentiate active lupus nephritis from inactive disease is clinically important.* -
  • The review assessed 40 studies involving 3,411 patients and identified 32 candidate urinary biomarkers, with 14 of them validated in multiple papers and showing strong diagnostic potential.* -
  • These urinary biomarkers can not only assist in diagnosis and monitoring of active lupus nephritis but also provide insights into the underlying kidney processes, suggesting that advancements in proteomics will enhance our understanding even further.*
View Article and Find Full Text PDF