Detail
Článek
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Intrarenal cytokine and chemokine gene expression and kidney graft outcome

P. Hribova, J. Lacha, K. Kotsch, H.D. Volk, I. Brabcova, J. Skibova, S. Vitko, O. Viklicky

. 2007 ; 30 (5) : 273-282.

Jazyk angličtina Země Švýcarsko

Typ dokumentu srovnávací studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc10012811

E-zdroje NLK

Karger Journals od 1996 do 2009
ProQuest Central od 1994-05-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2005-01-01
Health & Medicine (ProQuest) od 1994-05-01 do Před 1 rokem
ROAD: Directory of Open Access Scholarly Resources od 1996

AIMS: Proinflammatory cytokines are thought to play an important role in various kidney graft diseases resulting in interstitial fibrosis and tubular atrophy frequently found in case biopsies. To explore the role of various cytokines and chemokines in the long-term graft outcome, the transcription patterns of their genes in kidney allograft biopsies were evaluated. METHODS: The real-time RT-PCR was used to identify intragraft mRNA expression of cytokines and chemokines in 74 kidney graft recipients and the results were correlated with histological and clinical parameters and long-term graft outcome. RESULTS: We observed up-regulated IL-10 (p < 0.001), TGF-beta1, IL-6, MCP-1, RANTES (p < 0.01) and TNF-alpha (p < 0.05) mRNA expression in patients with chronic allograft nephropathy (CAN) as compared to controls. There were positive correlations between the mRNA expression of IL-6 (p < 0.001), IL-10 (p < 0.01), TNF-alpha, MCP-1 (p < 0.05) and the proteinuria. The up-regulation of intrarenal MCP-1 in patients with CAN increased the risk for the graft failure within the next 42 months (OR 5.1, p < 0.05). Kaplan-Meier survival analysis revealed that proteinuria and higher intragraft expression of TGF-beta1 and MCP-1 predict a poor kidney graft outcome. CONCLUSION: Expression patterns of intrarenal proinflammatory genes might discriminate patients at a higher risk for the earlier allograft failure. 2007 S. Karger AG, Basel

000      
03205naa 2200505 a 4500
001      
bmc10012811
003      
CZ-PrNML
005      
20130627204614.0
008      
100527s2007 sz e eng||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Hřibová, Petra $7 xx0143051
245    10
$a Intrarenal cytokine and chemokine gene expression and kidney graft outcome / $c P. Hribova, J. Lacha, K. Kotsch, H.D. Volk, I. Brabcova, J. Skibova, S. Vitko, O. Viklicky
314    __
$a Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
520    9_
$a AIMS: Proinflammatory cytokines are thought to play an important role in various kidney graft diseases resulting in interstitial fibrosis and tubular atrophy frequently found in case biopsies. To explore the role of various cytokines and chemokines in the long-term graft outcome, the transcription patterns of their genes in kidney allograft biopsies were evaluated. METHODS: The real-time RT-PCR was used to identify intragraft mRNA expression of cytokines and chemokines in 74 kidney graft recipients and the results were correlated with histological and clinical parameters and long-term graft outcome. RESULTS: We observed up-regulated IL-10 (p < 0.001), TGF-beta1, IL-6, MCP-1, RANTES (p < 0.01) and TNF-alpha (p < 0.05) mRNA expression in patients with chronic allograft nephropathy (CAN) as compared to controls. There were positive correlations between the mRNA expression of IL-6 (p < 0.001), IL-10 (p < 0.01), TNF-alpha, MCP-1 (p < 0.05) and the proteinuria. The up-regulation of intrarenal MCP-1 in patients with CAN increased the risk for the graft failure within the next 42 months (OR 5.1, p < 0.05). Kaplan-Meier survival analysis revealed that proteinuria and higher intragraft expression of TGF-beta1 and MCP-1 predict a poor kidney graft outcome. CONCLUSION: Expression patterns of intrarenal proinflammatory genes might discriminate patients at a higher risk for the earlier allograft failure. 2007 S. Karger AG, Basel
650    _2
$a dospělí $7 D000328
650    _2
$a chemokiny $x biosyntéza $x genetika $7 D018925
650    _2
$a cytokiny $x biosyntéza $x genetika $7 D016207
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a následné studie $7 D005500
650    _2
$a regulace genové exprese $x fyziologie $7 D005786
650    _2
$a rejekce štěpu $x genetika $x metabolismus $7 D006084
650    _2
$a přežívání štěpu $x genetika $7 D006085
650    _2
$a lidé $7 D006801
650    _2
$a ledviny $x metabolismus $x patologie $7 D007668
650    _2
$a transplantace ledvin $7 D016030
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a výsledek terapie $7 D016896
650    _2
$a financování organizované $7 D005381
655    _2
$a srovnávací studie $7 D003160
700    1_
$a Lácha, Jiří, $d 1960-2005 $7 nlk20010095504
700    1_
$a Kotsch, Katja
700    1_
$a Volk, Hans-Dieter
700    1_
$a Brabcová, Irena $7 xx0079327
700    1_
$a Skibová, Jelena $7 xx0061183
700    1_
$a Vítko, Štefan, $d 1953- $7 jn20000402658
700    1_
$a Viklický, Ondřej, $d 1966- $7 nlk20050170291
773    0_
$t Kidney & Blood Pressure Research $w MED00003064 $g Roč. 30, č. 5 (2007), s. 273-282
910    __
$a ABA008 $b x $y 8
990    __
$a 20100602083136 $b ABA008
991    __
$a 20130627205106 $b ABA008
999    __
$a ok $b bmc $g 726666 $s 589823
BAS    __
$a 3
BMC    __
$a 2007 $b 30 $c 5 $d 273-282 $m Kidney & blood pressure research $n Kidney Blood Press Res $x MED00003064
LZP    __
$a 2010-B2/vtme