Pregled bibliografske jedinice broj: 1162526
Immunophenotyping of chemokine receptors on peripheral blood mononuclear cells in children with type 1 diabetes
Immunophenotyping of chemokine receptors on peripheral blood mononuclear cells in children with type 1 diabetes // Annual meeting of of the Croatian Immunological Society 2019
Rovinj, Hrvatska, 2019. str. 51-51 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1162526 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Immunophenotyping of chemokine receptors on
peripheral blood mononuclear cells in children
with type 1 diabetes
Autori
Špehar Uroić, Anita ; Filipović, Maša ; Flegar, Darja ; Šućur, Alan ; Kovačić, Nataša ; Grčević, Danka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
Annual meeting of of the Croatian Immunological Society 2019
Mjesto i datum
Rovinj, Hrvatska, 11.10.2019. - 12.10.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
type 1 diabetes ; children ; chemokine receptors ; peripheral blood mononuclear cells
Sažetak
INTRODUCTION: Type 1 diabetes (T1D) is a chronic autoimmune disease characterized by insulin deficiency, hyperglycemia and metabolic disturbances. Chemokines contribute to low-grade inflammation, which predisposes to the development of vascular complications. Our aim was to determine the chemokine receptor phenotype on peripheral blood mononuclear cells (PBMCs) in children with T1D. METHODS: Mononuclear cells were isolated from peripheral blood of healthy controls (n=13) and children with T1D (n=22). B-cell (CD19+), T-cell (CD3+) and monocyte (CD14+) phenotype was determined using flow cytometry for the following chemokine receptors: CCR2, CCR4, CXCR3 and CXCR4. Frequencies of PBMC subpopulations expressing chemokine receptors were correlated with clinical parameters indicating disease activity (HbA1c and insulin dose), vascular complications (blood pressure and lipid profile) and inflammation (CRP and fibrinogen). RESULTS: Major immune population frequencies did not differ between groups, however there was a decrease of CCR2+ monocytes in T1D group (p=0.019) as well as expansion, though nonsignificant, of CCR4+ T-cells. Expression of CXCR3 and CXCR4 on PBMCs was similar among T1D patients and controls. Monocytes expressing CCR2 were negatively associated with HbA1c levels (ρ=-0.459) and T-cells expressing CCR4 were negatively associated with systolic blood pressure (ρ=-0.389). CONCLUSION: Because of the migratory role of CCR2, we propose the decrease in CCR2+ monocyte subpopulation is due to the increased peripheral sequestration that contributes to the disease pathogenesis and its vascular complications. In contrast, T-cells expressing CCR4 may have a protective role and are therefore, decreased, in children with vascular complications. SUPPORT: Croatian Science Foundation projects IP- 2018-01-2414, IP-2014-09-7406 and DOK2018-09-4276.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
IP-2018-01-2414 - Notch signaling in osteoclast progenitors induced by rheumatoid arthritis (NORA) (Grčević, Danka, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Nataša Kovačić
(autor)
Darja Flegar
(autor)
Danka Grčević
(autor)
Anita Špehar Uroić
(autor)
Alan Šućur
(autor)
Maša Filipović
(autor)