-
Je něco špatně v tomto záznamu ?
Contribution of non-HLA incompatibility between donor and recipient to kidney allograft survival: genome-wide analysis in a prospective cohort
R. Reindl-Schwaighofer, A. Heinzel, A. Kainz, J. van Setten, K. Jelencsics, K. Hu, BL. Loza, M. Kammer, G. Heinze, P. Hruba, A. Koňaříková, O. Viklicky, GA. Boehmig, F. Eskandary, G. Fischer, F. Claas, JC. Tan, TJ. Albert, J. Patel, B. Keating,...
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
NLK
ProQuest Central
od 1992-01-04 do Před 3 měsíci
Nursing & Allied Health Database (ProQuest)
od 1992-01-04 do Před 3 měsíci
Health & Medicine (ProQuest)
od 1992-01-04 do Před 3 měsíci
Family Health Database (ProQuest)
od 1992-01-04 do Před 3 měsíci
Psychology Database (ProQuest)
od 1992-01-04 do Před 3 měsíci
Health Management Database (ProQuest)
od 1992-01-04 do Před 3 měsíci
Public Health Database (ProQuest)
od 1992-01-04 do Před 3 měsíci
- MeSH
- alografty imunologie MeSH
- celogenomová asociační studie MeSH
- dárci tkání MeSH
- dospělí MeSH
- HLA antigeny imunologie MeSH
- hodnocení výsledků zdravotní péče MeSH
- jednonukleotidový polymorfismus MeSH
- Kaplanův-Meierův odhad MeSH
- lidé středního věku MeSH
- lidé MeSH
- přežívání štěpu * MeSH
- proporcionální rizikové modely MeSH
- prospektivní studie MeSH
- protilátky imunologie MeSH
- rejekce štěpu epidemiologie imunologie MeSH
- studie případů a kontrol MeSH
- testování histokompatibility statistika a číselné údaje MeSH
- transplantace ledvin statistika a číselné údaje MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: The introduction of HLA matching of donors and recipients was a breakthrough in kidney transplantation. However, half of all transplanted kidneys still fail within 15 years after transplantation. Epidemiological data suggest a fundamental role of non-HLA alloimmunity. METHODS: We genotyped 477 pairs of deceased donors and first kidney transplant recipients with stable graft function at three months that were transplanted between Dec 1, 2005, and April 30, 2015. Genome-wide genetic mismatches in non-synonymous single nucleotide polymorphisms (nsSNPs) were calculated to identify incompatibilities in transmembrane and secreted proteins. We estimated the association between nsSNP mismatch and graft loss in a Cox proportional hazard model, adjusting for HLA mismatch and clinical covariates. Customised peptide arrays were generated to screen for antibodies against genotype-derived mismatched epitopes in 25 patients with biopsy-confirmed chronic antibody-mediated rejection. FINDINGS: 59 268 nsSNPs affecting a transmembrane or secreted protein were analysed. The median number of nsSNP mismatches in immune-accessible transmembrane and secreted proteins between donors and recipients was 1892 (IQR 1850-1936). The degree of nsSNP mismatch was independently associated with graft loss in a multivariable model adjusted for HLA eplet mismatch (HLA-A, HLA-B, HLA-C, HLA-DP, HLA-DQ, and HLA-DR). Each increase by a unit of one IQR had an HR of 1·68 (95% CI 1·17-2·41, p=0·005). 5-year death censored graft survival was 98% in the quartile with the lowest mismatch, 91% in the second quartile, 89% in the third quartile, and 82% in the highest quartile (p=0·003, log-rank test). Customised peptide arrays verified a donor-specific alloimmune response to genetically predicted mismatched epitopes. INTERPRETATION: Genetic mismatch of non-HLA haplotypes coding for transmembrane or secreted proteins is associated with an increased risk of functional graft loss independently of HLA incompatibility. As in HLA alloimmunity, donor-specific alloantibodies can be identified against genotype derived non-HLA epitopes. FUNDING: Austrian Science Fund, WWTF (Vienna Science and Technology Fund), and Ministry of Health of the Czech Republic.
Department of Cardiology University Medical Center Utrecht University of Utrecht Utrecht Netherlands
Department of Nephrology Medical University of Vienna Vienna Austria
Department of Surgery University of Pennsylvania Philadelphia PA USA
Transplant Laboratory Institute for Clinical and Experimental Medicine Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19027806
- 003
- CZ-PrNML
- 005
- 20190823092908.0
- 007
- ta
- 008
- 190813s2019 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/S0140-6736(18)32473-5 $2 doi
- 035 __
- $a (PubMed)30773281
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Reindl-Schwaighofer, Roman $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 245 10
- $a Contribution of non-HLA incompatibility between donor and recipient to kidney allograft survival: genome-wide analysis in a prospective cohort / $c R. Reindl-Schwaighofer, A. Heinzel, A. Kainz, J. van Setten, K. Jelencsics, K. Hu, BL. Loza, M. Kammer, G. Heinze, P. Hruba, A. Koňaříková, O. Viklicky, GA. Boehmig, F. Eskandary, G. Fischer, F. Claas, JC. Tan, TJ. Albert, J. Patel, B. Keating, R. Oberbauer, iGeneTRAiN consortium,
- 520 9_
- $a BACKGROUND: The introduction of HLA matching of donors and recipients was a breakthrough in kidney transplantation. However, half of all transplanted kidneys still fail within 15 years after transplantation. Epidemiological data suggest a fundamental role of non-HLA alloimmunity. METHODS: We genotyped 477 pairs of deceased donors and first kidney transplant recipients with stable graft function at three months that were transplanted between Dec 1, 2005, and April 30, 2015. Genome-wide genetic mismatches in non-synonymous single nucleotide polymorphisms (nsSNPs) were calculated to identify incompatibilities in transmembrane and secreted proteins. We estimated the association between nsSNP mismatch and graft loss in a Cox proportional hazard model, adjusting for HLA mismatch and clinical covariates. Customised peptide arrays were generated to screen for antibodies against genotype-derived mismatched epitopes in 25 patients with biopsy-confirmed chronic antibody-mediated rejection. FINDINGS: 59 268 nsSNPs affecting a transmembrane or secreted protein were analysed. The median number of nsSNP mismatches in immune-accessible transmembrane and secreted proteins between donors and recipients was 1892 (IQR 1850-1936). The degree of nsSNP mismatch was independently associated with graft loss in a multivariable model adjusted for HLA eplet mismatch (HLA-A, HLA-B, HLA-C, HLA-DP, HLA-DQ, and HLA-DR). Each increase by a unit of one IQR had an HR of 1·68 (95% CI 1·17-2·41, p=0·005). 5-year death censored graft survival was 98% in the quartile with the lowest mismatch, 91% in the second quartile, 89% in the third quartile, and 82% in the highest quartile (p=0·003, log-rank test). Customised peptide arrays verified a donor-specific alloimmune response to genetically predicted mismatched epitopes. INTERPRETATION: Genetic mismatch of non-HLA haplotypes coding for transmembrane or secreted proteins is associated with an increased risk of functional graft loss independently of HLA incompatibility. As in HLA alloimmunity, donor-specific alloantibodies can be identified against genotype derived non-HLA epitopes. FUNDING: Austrian Science Fund, WWTF (Vienna Science and Technology Fund), and Ministry of Health of the Czech Republic.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a alografty $x imunologie $7 D064591
- 650 _2
- $a protilátky $x imunologie $7 D000906
- 650 _2
- $a studie případů a kontrol $7 D016022
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a celogenomová asociační studie $7 D055106
- 650 _2
- $a rejekce štěpu $x epidemiologie $x imunologie $7 D006084
- 650 12
- $a přežívání štěpu $7 D006085
- 650 _2
- $a HLA antigeny $x imunologie $7 D006680
- 650 _2
- $a testování histokompatibility $x statistika a číselné údaje $7 D006650
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a Kaplanův-Meierův odhad $7 D053208
- 650 _2
- $a transplantace ledvin $x statistika a číselné údaje $7 D016030
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a hodnocení výsledků zdravotní péče $7 D017063
- 650 _2
- $a jednonukleotidový polymorfismus $7 D020641
- 650 _2
- $a proporcionální rizikové modely $7 D016016
- 650 _2
- $a prospektivní studie $7 D011446
- 650 _2
- $a dárci tkání $7 D014019
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Heinzel, Andreas $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Kainz, Alexander $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a van Setten, Jessica $u Department of Cardiology, University Medical Center Utrecht, University of Utrecht, Utrecht, Netherlands.
- 700 1_
- $a Jelencsics, Kira $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Hu, Karin $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Loza, Bao-Li $u Department of Surgery, University of Pennsylvania, Philadelphia, PA, USA.
- 700 1_
- $a Kammer, Michael $u Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Heinze, Georg $u Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Hruba, Petra $u Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
- 700 1_
- $a Koňaříková, Alena $u Department of Nephrology, Transplant Center, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
- 700 1_
- $a Viklicky, Ondrej $u Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic; Department of Nephrology, Transplant Center, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
- 700 1_
- $a Boehmig, Georg A $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Eskandary, Farsad $u Department of Nephrology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Fischer, Gottfried $u Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Claas, Frans $u Department of Immunohematology and Blood Transfusion, Leiden University Medical Centre, Leiden, Netherlands.
- 700 1_
- $a Tan, John C $u Roche Madison, Madison, WI, USA.
- 700 1_
- $a Albert, Tom J $u Roche Madison, Madison, WI, USA.
- 700 1_
- $a Patel, Jigar $u Roche Madison, Madison, WI, USA.
- 700 1_
- $a Keating, Brendan $u Department of Surgery, University of Pennsylvania, Philadelphia, PA, USA.
- 700 1_
- $a Oberbauer, Rainer $u Department of Nephrology, Medical University of Vienna, Vienna, Austria. Electronic address: rainer.oberbauer@meduniwien.ac.at.
- 710 2_
- $a iGeneTRAiN consortium
- 773 0_
- $w MED00010161 $t Lancet (London, England) $x 1474-547X $g Roč. 393, č. 10174 (2019), s. 910-917
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30773281 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20190823093123 $b ABA008
- 999 __
- $a ok $b bmc $g 1432955 $s 1066266
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 393 $c 10174 $d 910-917 $e 20190214 $i 1474-547X $m Lancet $n Lancet $x MED00010161
- LZP __
- $a Pubmed-20190813