<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Spitznagel T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Indication biopsies for deterioration of kidney allograft function often require follow-up biopsies to assess treatment response or lack of improvement. Immune-mediated injury, namely borderline rejection (BLR), T-cell mediated rejection (TCMR), or antibody-mediated rejection (ABMR), results from preformed or &lt;i>de novo&lt;/i> alloreactivity due to donor and recipient HLA-mismatches. The impact of HLA-mismatches on alloreactivity is determined by highly immunogenic HLA-epitopes.&lt;h4>Methods&lt;/h4>We analyzed 123 kidney transplant recipients (KTRs) from 2009 to 2019 who underwent a first indication and a follow-up biopsy. KTRs were divided into three groups according to the first biopsy: No rejection (NR)/BLR (n=68); TCMR (n=21); ABMR (n=34). The HLA-derived epitope-mismatches </pubmed_abstract><journal>Frontiers in immunology</journal><pagination>949933</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9428698</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PIRCHE-II scores prove useful as a predictive biomarker among kidney transplant recipients with rejection: An analysis of indication and follow-up biopsies.</pubmed_title><pmcid>PMC9428698</pmcid><pubmed_authors>von Moos S</pubmed_authors><pubmed_authors>Schachtner T</pubmed_authors><pubmed_authors>Nilsson J</pubmed_authors><pubmed_authors>Kaufmann YL</pubmed_authors><pubmed_authors>Matter LS</pubmed_authors><pubmed_authors>Spitznagel T</pubmed_authors></additional><is_claimable>false</is_claimable><name>PIRCHE-II scores prove useful as a predictive biomarker among kidney transplant recipients with rejection: An analysis of indication and follow-up biopsies.</name><description>&lt;h4>Background&lt;/h4>Indication biopsies for deterioration of kidney allograft function often require follow-up biopsies to assess treatment response or lack of improvement. Immune-mediated injury, namely borderline rejection (BLR), T-cell mediated rejection (TCMR), or antibody-mediated rejection (ABMR), results from preformed or &lt;i>de novo&lt;/i> alloreactivity due to donor and recipient HLA-mismatches. The impact of HLA-mismatches on alloreactivity is determined by highly immunogenic HLA-epitopes.&lt;h4>Methods&lt;/h4>We analyzed 123 kidney transplant recipients (KTRs) from 2009 to 2019 who underwent a first indication and a follow-up biopsy. KTRs were divided into three groups according to the first biopsy: No rejection (NR)/BLR (n=68); TCMR (n=21); ABMR (n=34). The HLA-derived epitope-mismatches </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-05T12:11:00.163Z</modification><creation>2025-04-05T12:11:00.163Z</creation></dates><accession>S-EPMC9428698</accession><cross_references><pubmed>36059499</pubmed><doi>10.3389/fimmu.2022.949933</doi></cross_references></HashMap>