-
Je něco špatně v tomto záznamu ?
Molecular profiling of acute and chronic rejections of renal allografts
H. Petra, H. Eva, B. Irena, H. Petra, V. Ondřej,
Jazyk angličtina Země Egypt
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2003
Free Medical Journals
od 1990
PubMed Central
od 2003 do 2013
Europe PubMed Central
od 2003 do 2013
Open Access Digital Library
od 2003-01-01 do 2013-12-31
Open Access Digital Library
od 2003-01-01 do 2013-12-31
Open Access Digital Library
od 2003-01-01
Medline Complete (EBSCOhost)
od 2003-03-01 do 2013-01-31
ROAD: Directory of Open Access Scholarly Resources
od 2003 do 2013
PubMed
24302958
DOI
10.1155/2013/509259
Knihovny.cz E-zdroje
- MeSH
- alografty imunologie metabolismus MeSH
- biopsie MeSH
- dospělí MeSH
- hodnocení výsledků pacienta MeSH
- ledviny imunologie metabolismus patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- prognóza MeSH
- regulace genové exprese MeSH
- rejekce štěpu genetika imunologie mortalita MeSH
- rizikové faktory MeSH
- ROC křivka MeSH
- shluková analýza MeSH
- stanovení celkové genové exprese * MeSH
- transkriptom MeSH
- transplantace ledvin škodlivé účinky MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Both antibody mediated (AMR) and T-cell mediated (TCMR) rejections either acute or chronic represent the main reason for late graft dysfunction. In this study we aimed to evaluate differences in the intrarenal expression patterns of immune system related genes in acute and chronic rejections. Graft biopsies were performed and evaluated according to Banff classification. Using the TaqMan Low Density Array, the intrarenal expressions of 376 genes relating to immune response (B-cell activation, T-cell activation, chemokines, growth factors, immune regulators, and apoptosis) were analyzed in the four rejection categories: chronic AMR, chronic TCMR, acute AMR, and acute TCMR. The set of genes significantly upregulated in acute TCMR as compared to acute AMR was identified, while no difference in gene expressions between chronic rejections groups was found. In comparison with functioning grafts, grafts that failed within the next 24 months after the chronic rejection morphological confirmation presented at biopsy already established severe graft injury (low eGFR, higher proteinuria), longer followup, higher expression of CDC20, CXCL6, DIABLO, GABRP, KIAA0101, ME2, MMP7, NFATC4, and TGFB3 mRNA, and lower expression of CCL19 and TRADD mRNA. In conclusion, both Banff 2007 chronic rejection categories did not differ in intrarenal expression of 376 selected genes associated with immune response.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14063825
- 003
- CZ-PrNML
- 005
- 20140708102733.0
- 007
- ta
- 008
- 140704s2013 ua f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1155/2013/509259 $2 doi
- 035 __
- $a (PubMed)24302958
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ua
- 100 1_
- $a Petra, Hřibová $u Transplant Laboratory, Institute for Clinical and Experimental Medicine, Vídeňská 1958/9, 14021 Prague, Czech Republic.
- 245 10
- $a Molecular profiling of acute and chronic rejections of renal allografts / $c H. Petra, H. Eva, B. Irena, H. Petra, V. Ondřej,
- 520 9_
- $a Both antibody mediated (AMR) and T-cell mediated (TCMR) rejections either acute or chronic represent the main reason for late graft dysfunction. In this study we aimed to evaluate differences in the intrarenal expression patterns of immune system related genes in acute and chronic rejections. Graft biopsies were performed and evaluated according to Banff classification. Using the TaqMan Low Density Array, the intrarenal expressions of 376 genes relating to immune response (B-cell activation, T-cell activation, chemokines, growth factors, immune regulators, and apoptosis) were analyzed in the four rejection categories: chronic AMR, chronic TCMR, acute AMR, and acute TCMR. The set of genes significantly upregulated in acute TCMR as compared to acute AMR was identified, while no difference in gene expressions between chronic rejections groups was found. In comparison with functioning grafts, grafts that failed within the next 24 months after the chronic rejection morphological confirmation presented at biopsy already established severe graft injury (low eGFR, higher proteinuria), longer followup, higher expression of CDC20, CXCL6, DIABLO, GABRP, KIAA0101, ME2, MMP7, NFATC4, and TGFB3 mRNA, and lower expression of CCL19 and TRADD mRNA. In conclusion, both Banff 2007 chronic rejection categories did not differ in intrarenal expression of 376 selected genes associated with immune response.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a alografty $x imunologie $x metabolismus $7 D064591
- 650 _2
- $a biopsie $7 D001706
- 650 _2
- $a shluková analýza $7 D016000
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 12
- $a stanovení celkové genové exprese $7 D020869
- 650 _2
- $a regulace genové exprese $7 D005786
- 650 _2
- $a rejekce štěpu $x genetika $x imunologie $x mortalita $7 D006084
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a ledviny $x imunologie $x metabolismus $x patologie $7 D007668
- 650 _2
- $a transplantace ledvin $x škodlivé účinky $7 D016030
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a hodnocení výsledků pacienta $7 D063868
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a ROC křivka $7 D012372
- 650 _2
- $a rizikové faktory $7 D012307
- 650 _2
- $a transkriptom $7 D059467
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Eva, Honsová
- 700 1_
- $a Irena, Brabcová
- 700 1_
- $a Petra, Hrubá
- 700 1_
- $a Ondřej, Viklický
- 773 0_
- $w MED00013777 $t Clinical & developmental immunology $x 1740-2530 $g Roč. 2013, č. - (2013), s. 509259
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24302958 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20140704 $b ABA008
- 991 __
- $a 20140708103023 $b ABA008
- 999 __
- $a ok $b bmc $g 1031309 $s 862557
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 2013 $c - $d 509259 $i 1740-2530 $m Clinical & developmental immunology $n Clin Dev Immunol $x MED00013777
- LZP __
- $a Pubmed-20140704