Skip to main content
Have a personal or library account? Click to login
Soluble CD163 as a Non-Invasive Biomarker in Autoimmune Nephrological and Rheumatological Diseases Cover

Soluble CD163 as a Non-Invasive Biomarker in Autoimmune Nephrological and Rheumatological Diseases

Open Access
|Sep 2026

Figures & Tables

Table 1.

Overview of clinical applications and key observations of CD163 in autoimmune nephrological and rheumatic diseases (Jude et al. 2013; Zhang et al. 2020; Gong et al. 2021; Moran et al. 2021)

DiseaseBiomarkerKey clinical applicationKey observationsStatistical significance
LNusCD163Diagnosis of active LN, assessment of response to treatmentCorrelation with activity index (not chronicity), decrease after treatmentAUROC 0.89–0.998
IgANusCD163Stratification of the risk of events related to kidney disease progressionIt correlates with the infiltration of CD163-positive macrophages in the tubulointerstitium, but not in the glomeruliAUROC 0.788
AAVusCD163Diagnosis of active renal vasculitis, ruling out active disease without biopsyHigh negative predictive valueAUROC 0.95
RAsCD163Monitoring disease activity in early RA, predicting the progression of radiological changes, potential significance in dose taperingCorrelation with DAS8 in early RA, no correlation in LSRAStrong correlation with IL-12 and CXCL (r = 0.99, both) in LSRA
SpAsCD163Reflects local synovial macrophage activation rather than systemic inflammationM2-like phenotype in SpA is shaped by local cytokine gradients at the synovial surfaceN/A (mainly qualitative/quantitative observations)
PMRsCD163Monitoring subclinical disease activity during treatment (indirectly from GCA studies)At least 52 weeks of IL-6 pathway inhibition may be needed to reset inflammatory mechanismsN/A (data mainly from GCA, no studies in isolated PMR)
FibromialgiaMissingPotential negative discriminatorNegative discriminator between inflammatory and non-inflammatory musculoskeletal painHypothesis for future research

[i] AAV, ANCA-associated vasculitis; AUROC, area under the receiver operating characteristic; GCA, giant cell arteritis; IgAN, IgA nephropathy; IL, interleukin; LN, lupus nephritis; LSRA, long-standing rheumatoid arthritis; PMR, polymyalgia rheumatic; RA, rheumatoid arthritis; sCD163, soluble CD163; SpA, spondyloarthritis; usCD163, urinary soluble CD163.

Fig 1.

Compartmentalization of clinical information carried by sCD163 in kidney and joint diseases (Matsushita et al. 2002; Baeten et al. 2004; Etzerodt and Moestrup 2013; Mejia-Vilet et al. 2020; Zhang et al. 2020). sCD163, soluble CD163; usCD163, urinary soluble CD163; sfCD163: synovial fluid sCD163.

Language: English
Submitted on: Feb 28, 2026
Accepted on: Jun 18, 2026
Published on: Sep 1, 2026
Published by: Hirszfeld Institute of Immunology and Experimental Therapy
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2026 Dorota Kamińska, Paweł Poznański, Wojciech Tański, Anna Skotny, published by Hirszfeld Institute of Immunology and Experimental Therapy
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.