Pre-transplant donor-specific Interferon-gamma-producing cells and acute rejection of the kidney allograft
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F15%3A00059552" target="_blank" >RIV/00023001:_____/15:00059552 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.sciencedirect.com/science/article/pii/S0966327415300125" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0966327415300125</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.trim.2015.07.007" target="_blank" >10.1016/j.trim.2015.07.007</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Pre-transplant donor-specific Interferon-gamma-producing cells and acute rejection of the kidney allograft
Popis výsledku v původním jazyce
Background: Our retrospective study included a cohort of 47 patients who underwent living donor kidney transplantation. The pre-transplant frequencies of donor-specific Interferon-gamma (IFN-gamma) producing cells were defined using enzyme-linked immunosorbent spot (ELISpot) assay and correlated with incidence of acute cellular (ACR), antibody-mediated rejection (AMR) and kidney graft survival up to one year after transplantation. Results: We found a statistically significant correlation between the frequencies of IFN-gamma-producing cells and the number of mismatches in HLA antigens between patients and their respective donors - for Class I - A and B (r = 0399, p <0.01) and for Class land Class II antigens - A, B and DR Cr = 0.409,p <0.01). No significant relationship was observed between the numbers of IFN-gamma-secreting cells and incidence of acute rejection (neither ACR, nor AMR). However, there was a trend of elevated frequencies of IFN-gamma-producing cells in patients who developed ACR or AMR in comparison with kidney recipients free of rejection (91 82 and 114 75 vs. 72 70/5 x 10(4) peripheral blood mononuclear cells respectively). Patients with concurrent acute cellular and antibody-mediated rejection had also higher numbers of IFN-y-producing memory/effector cells compared to patients with cellular rejection only. Conclusion: Pre-transplant determination of the numbers of IFN-y-producing donor-specific memory cells using the ELISpot technique may provide clinically relevant results when evaluating the risk of development of acute cellular and antibody-mediated rejection. These frequencies are influenced by the degree of HLA mismatching between patients and their respective kidney donors.
Název v anglickém jazyce
Pre-transplant donor-specific Interferon-gamma-producing cells and acute rejection of the kidney allograft
Popis výsledku anglicky
Background: Our retrospective study included a cohort of 47 patients who underwent living donor kidney transplantation. The pre-transplant frequencies of donor-specific Interferon-gamma (IFN-gamma) producing cells were defined using enzyme-linked immunosorbent spot (ELISpot) assay and correlated with incidence of acute cellular (ACR), antibody-mediated rejection (AMR) and kidney graft survival up to one year after transplantation. Results: We found a statistically significant correlation between the frequencies of IFN-gamma-producing cells and the number of mismatches in HLA antigens between patients and their respective donors - for Class I - A and B (r = 0399, p <0.01) and for Class land Class II antigens - A, B and DR Cr = 0.409,p <0.01). No significant relationship was observed between the numbers of IFN-gamma-secreting cells and incidence of acute rejection (neither ACR, nor AMR). However, there was a trend of elevated frequencies of IFN-gamma-producing cells in patients who developed ACR or AMR in comparison with kidney recipients free of rejection (91 82 and 114 75 vs. 72 70/5 x 10(4) peripheral blood mononuclear cells respectively). Patients with concurrent acute cellular and antibody-mediated rejection had also higher numbers of IFN-y-producing memory/effector cells compared to patients with cellular rejection only. Conclusion: Pre-transplant determination of the numbers of IFN-y-producing donor-specific memory cells using the ELISpot technique may provide clinically relevant results when evaluating the risk of development of acute cellular and antibody-mediated rejection. These frequencies are influenced by the degree of HLA mismatching between patients and their respective kidney donors.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FN - Epidemiologie, infekční nemoci a klinická imunologie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/NT14022" target="_blank" >NT14022: DONOR-SPECIFICKÉ INTERFERON-GAMA PRODUKUJÍCÍ BUŇKY A PREDIKCE REJEKCE TRANSPLANTOVANÉ LEDVINY</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Transplant immunology
ISSN
0966-3274
e-ISSN
—
Svazek periodika
33
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
6
Strana od-do
63-68
Kód UT WoS článku
000363818200003
EID výsledku v databázi Scopus
—