Pregled bibliografske jedinice broj: 1106420
Potential Immune Biomarkers in Diagnosis and Clinical Management for Systemic Lupus Erythematosus
Potential Immune Biomarkers in Diagnosis and Clinical Management for Systemic Lupus Erythematosus // Journal of Medical Biochemistry, 37 (2018), 2; 163-171 doi:10.1515/jomb-2017-0048 (međunarodna recenzija, članak, ostalo)
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Naslov
Potential Immune Biomarkers in Diagnosis and Clinical Management for Systemic Lupus Erythematosus
Autori
Zecevic, Lamija ; Karamehic, Jasenko ; Coric, Jozo ; Stubljar, David ; Avdagic, Nesina ; Selmanovic, Kenan ; Jukic, Tomislav ; Savic, Sinisa
Izvornik
Journal of Medical Biochemistry (1452-8258) 37
(2018), 2;
163-171
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, ostalo
Ključne riječi
SLE, biomarkers, T and B lymphocytes, cyto -kines, flow cytometry
Sažetak
Background: There is still no reliable, specific biomarker for precision diagnosis and clinical monitoring of systemic lupus erythematosus. The aim of this study was to investigate the importance of the determination of immunofenotypic profiles (T, B lymphocytes and NK cells) and serum cytokine concentrations (IL-17 and IFN-alpha) as potential biomarkers for this disease. Methods: The study included 55 patients with SLE and 25 healthy controls. The proportion of T, B, NK cells were assessed in peripheral blood using flow cytometric assays while the serum cytokine concentration (IL-17 and IFNalpha) was determined by ELISA test. Results: ROC curve analysis showed good accuracy to distinguish between patients and healthy individuals for activated T cells (A U C = 0.798 ; p < 0.001), Treg (AUC = 0.651 ; p = 0.036), and memory B cells (A U C = 0.285 ; p = 0.002). We found statistically significant difference (p = 0.036) in the levels of serum IL-17 between patients with SLE (IL-17= 49.27 pg/mL) and controls (IL-17 = 28.64 pg/mL). Conclusions: Significant increase in the relative number of Treg lymphocytes, and decrease in memory B cells, as well as decrease level of IL-17, in SLE patients may be implicated in the pathogenesis of the disease. These parameters, as biomarkers, could distinguish SLE patients and no-SLE patients. Monitoring subpopulations of immune cells in peripheral blood using flow cytometry provides insight into abnormal T and B cell function in SLE. Progress in understanding the immunity at SLE, results in concrete benefits for the SLE patients, which include new clinical management and therapeutic strategies.
Izvorni jezik
Engleski
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus