<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ye J</submitter><funding>Natural Science Foundation of Zhejiang Province</funding><pagination>778500</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8739481</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>&lt;b>Background:&lt;/b> Biliary atresia (BA) is considered to be an autoimmune-mediating inflammatory injury. The pathogenesis of BA has been proposed with the clonal transformation of T cells expressing analogous T-cell receptor β-chain variable regions (TRBVs). &lt;b>Methods:&lt;/b> The TRBV profile of the peripheral blood mononuclear cells (PBMCs) in infants with BA and control infants (healthy donors, HDs), respectively, were characterized by using high-throughput sequencing (HTS). The diversity of T cells was analyzed based on the frequency of complementarity-determining region 3 (CDR3) or V(CDR3)J. Moreover, the correlation between absolute lymphocyte count (ALC) and lactate dehydrogenase (LDH) or diversity (clonality) indices, respectively, were analyzed for subjects with BA and HD. &lt;b>Results</pubmed_abstract><journal>Frontiers in medicine</journal><pubmed_title>Altered T-Cell Receptor β-Chain and Lactate Dehydrogenase Are Associated With the Immune Pathogenesis of Biliary Atresia.</pubmed_title><pmcid>PMC8739481</pmcid><funding_grant_id>LY19H190004</funding_grant_id><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Shu Q</pubmed_authors><pubmed_authors>Lai D</pubmed_authors><pubmed_authors>Cao D</pubmed_authors><pubmed_authors>Hu L</pubmed_authors><pubmed_authors>Ye J</pubmed_authors><pubmed_authors>Zha H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Altered T-Cell Receptor β-Chain and Lactate Dehydrogenase Are Associated With the Immune Pathogenesis of Biliary Atresia.</name><description>&lt;b>Background:&lt;/b> Biliary atresia (BA) is considered to be an autoimmune-mediating inflammatory injury. The pathogenesis of BA has been proposed with the clonal transformation of T cells expressing analogous T-cell receptor β-chain variable regions (TRBVs). &lt;b>Methods:&lt;/b> The TRBV profile of the peripheral blood mononuclear cells (PBMCs) in infants with BA and control infants (healthy donors, HDs), respectively, were characterized by using high-throughput sequencing (HTS). The diversity of T cells was analyzed based on the frequency of complementarity-determining region 3 (CDR3) or V(CDR3)J. Moreover, the correlation between absolute lymphocyte count (ALC) and lactate dehydrogenase (LDH) or diversity (clonality) indices, respectively, were analyzed for subjects with BA and HD. &lt;b>Results</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T05:32:13.752Z</modification><creation>2022-02-11T15:05:59.58Z</creation></dates><accession>S-EPMC8739481</accession><cross_references><pubmed>35004747</pubmed><doi>10.3389/fmed.2021.778500</doi></cross_references></HashMap>