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231225s2021 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2021.108792
|2 doi
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|a pubmed24n1092.xml
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|a (DE-627)NLM327645075
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|a (NLM)34217849
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|a (PII)S1521-6616(21)00129-7
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Millán, Olga
|e verfasserin
|4 aut
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|a Advantages of plasmatic CXCL-10 as a prognostic and diagnostic biomarker for the risk of rejection and subclinical rejection in kidney transplantation
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|c 2021
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 16.09.2021
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|a Date Revised 16.09.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2021 Elsevier Inc. All rights reserved.
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|a This study evaluate the potential of plasmatic CXCL-10 (pCXCL-10) as a pre&post transplantation prognostic and diagnostic biomarker of T-cell-mediated rejection (TCMR), antibody-mediated rejection (ABMR) and subclinical rejection (SCR) risk in adult kidney recipients considering BKV and CMV infections as possible clinical confounder factors. Twenty-eight of 100 patients included experienced rejection (TCMR:14; ABMR:14); 8 SCR; 13 and 16 were diagnosed with BKV and CMV infection, respectively. Pre-transplantation pCXCL-10 was significantly increased in TCMR and ABMR and post-transplantation in TCMR, ABMR and SCR compared with nonrejectors. All CMV+ patients showed pCXCL-10 levels above the cutoff values established for rejection whereas the 80% of BKV+ patients showed pCXCL-10 concentration < 100 pg/mL. pCXCL-10 could improve pre-transplantation patient stratification and immunosuppressive treatment selection according to rejection risk; and after kidney transplantation could be a potential early prognostic biomarker for rejection. Clinical confounding factor in BKV+ and particularly in CMV+ patients must be discarded
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|a Journal Article
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|a Multicenter Study
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|a Observational Study
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|a Research Support, Non-U.S. Gov't
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|a ABMR
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|a BKV
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|a Biological matrix
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|a CMV
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|a CXCL-10
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|a Kidney transplantation
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|a Rejection (TCMR
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|a SCR)
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|a Biomarkers
|2 NLM
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|a CXCL10 protein, human
|2 NLM
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|a Chemokine CXCL10
|2 NLM
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|a Isoantibodies
|2 NLM
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|a Rovira, Jordi
|e verfasserin
|4 aut
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|a Guirado, Lluis
|e verfasserin
|4 aut
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|a Espinosa, Cristina
|e verfasserin
|4 aut
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|a Budde, Klemens
|e verfasserin
|4 aut
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|a Sommerer, Claudia
|e verfasserin
|4 aut
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|a Piñeiro, Gaston J
|e verfasserin
|4 aut
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|a Diekmann, Fritz
|e verfasserin
|4 aut
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|a Brunet, Mercè
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 229(2021) vom: 15. Aug., Seite 108792
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:229
|g year:2021
|g day:15
|g month:08
|g pages:108792
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|u http://dx.doi.org/10.1016/j.clim.2021.108792
|3 Volltext
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|a GBV_ILN_350
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|a AR
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|d 229
|j 2021
|b 15
|c 08
|h 108792
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