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. Author manuscript; available in PMC: 2022 May 15.
Published in final edited form as: J Autoimmun. 2020 Sep 4;115:102540. doi: 10.1016/j.jaut.2020.102540

Table 1.

Summary of the Published Studies about EVs in LN

EVs origin Cellular origin Markers Associated Specific component Samples Techniques for analyzing characteristics Study findings References Year
MVs Podocyte Annexin V/Podocalyxin NA Urine Flow cytometry Higher podocyte-derived MVs in LN and correlate with high activity indices, and increased proteinuria [151] 2019
MVs Mainly leukocytes Platelet CD41a; leukocyte CD45; erythrocyte CD235a HMGB1/HLA-DR/CX3CR1 PPP/Urine Flow cytometry High frequencies of MP-HMGB1+ in circulation and urine of LN patients. Urinary MP-HMGB1+ could discriminate between patients with active and inactive LN. [117] 2019
MVs Mainly platelets Mitochondria mitoTracker/TOM20/HK1; Platelet CD42a; T cell CD3 Nucleic acids/IgG Frozen PPP Flow cytometry Patients with signs of ongoing renal lupus activity (BILAG, A-C) had higher levels of mitoMVs and IgG-coated mitoMVs. [167] 2019
MVs Apoptotic endothelial cells KM-2/LG11–2 Acetylated chromatin PPP Flow cytometry MVs containing acetylated chromatin drive ROS independent NET release in SLE patients with active LN. [168] 2017
MVs NA Annexin V/G3BP G3BP, C1q, immunoglobulins PPP Flow cytometry/Co-localization immune electron microscopy(IEM)/Nano-LC-MS/MS Co-localization of G3BP positive MVs associated with ICs may deposit in the LN kidneys. [22] 2015
MVs Platelet/endothelial cell Platelet Annexin V/CD41; endothelial cell Annexin V/CD62E NA PPP Flow cytometry High circulatory platelet microparticles and endothelial microparticles in LN patients can be used as new markers for dysfunctional platelet activation and endothelium. [169] 2015
Exo Tubular renal cells NA MiR-31/MiR-107/MiR-135b-5p Urine NanoSight/Cryo-TEM/Western blot Urinary exosomal miR-135b-5p, miR-107, and miR-31 are promising novel markers for clinical outcomes, regulating LN renal recovery by HIF1A inhibition. [166] 2020
Exo NA CD9/TSG101 Let-7a/MiR-21 Urine NanoSight/Transmission electron microscopy (TEM)/Western blot Down-regulation of let-7a and miR-21 in urine exosomes from LN patients during disease flare. [164] 2018
Exo NA CD9/CD81 MiR-3135b/MiR-654–5p/MiR-146a-5p Urine Transmission electron microscopy (TEM)/Western blot LNIV-CC has a unique miRNA expression profile of urinary exosome and miR-3135b, miR-654–5p and miR-146a-5p in urinary exosomes could predict LNIV-CC. [170] 2018
Exo NA CD9/AQP2/TSG101 MiR-29c Urine Electron microscopy Western blot Decreased miR-29c in exosomes in LN is associated with increased renal chronicity and predict early renal fibrosis in LN. [165] 2015
Exo NA CD9/TSG101 MiR-146a Urine Transmission electron microscopy (TEM)/Western blot Exosomal miR-146a discriminates the presence of active LN. [162] 2015
Exo NA NA MiR-26a Urine NA Increased miR-26a levels in urinary exosomes may serve as a marker of injured podocytes in LN. [163] 2014
ABs NA NA NA Renal tissue Periodic acid-Schiff methenamine silver The presence of large numbers of apoptotic bodies in the glomeruli of Clq-deficient mice. [171] 1998
ABs NA NA NA Renal tissue Electron microscopy The presence of apoptotic cells and apoptotic bodies in proliferated mesangial areas and within the glomerular capillaries. [172] 1995

MVs (Microvesicles), mitoMVs (mitochondria MVs), Exo (Exosomes), ABs (Apoptotic Bodies), PPP (platelet poor plasma), LNIV-CC ( Type IV lupus nephritis-cellular crescent), ROS (Reactive oxygen species), LN (Lupus Nephritis), ICs (Immune Complexes), HMGB1 (High-mobility group box 1), G3BP (Galectin-3 binding protein), HK1 (anti-hexokinase 1).