<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Chang YH</submitter><pubmed_abstract>The repertoire of IgG antibody responses to infection and vaccination varies depending on the characteristics of the immunogen and the ability of the host to mount a protective immune response. Chronic hepatitis B virus (HBV) infections are marked by persistent infection and immune tolerance to vaccination. This disease offers a unique opportunity to discover key repertoire signatures during infection and in response to vaccination. Complementarity determining region 3 of an antibody heavy chain (CDR-H3) has a major impact on the antigenic specificity of an antibody. We used next-generation sequencing to characterize the CDR-H3 sequences in paired siblings of 4 families in which only one member of each pair had chronic HBV infection. Blood samples were obtained before and 2 weeks after HBV</pubmed_abstract><journal>Scientific reports</journal><pagination>26556</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4879636</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Network Signatures of IgG Immune Repertoires in Hepatitis B Associated Chronic Infection and Vaccination Responses.</pubmed_title><pmcid>PMC4879636</pmcid><pubmed_authors>Chang YH</pubmed_authors><pubmed_authors>Ma KH</pubmed_authors><pubmed_authors>Hsieh TC</pubmed_authors><pubmed_authors>Tsai SF</pubmed_authors><pubmed_authors>Liu HH</pubmed_authors><pubmed_authors>Hsu WB</pubmed_authors><pubmed_authors>Kuan HC</pubmed_authors><pubmed_authors>Yang CH</pubmed_authors><pubmed_authors>Chao A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Network Signatures of IgG Immune Repertoires in Hepatitis B Associated Chronic Infection and Vaccination Responses.</name><description>The repertoire of IgG antibody responses to infection and vaccination varies depending on the characteristics of the immunogen and the ability of the host to mount a protective immune response. Chronic hepatitis B virus (HBV) infections are marked by persistent infection and immune tolerance to vaccination. This disease offers a unique opportunity to discover key repertoire signatures during infection and in response to vaccination. Complementarity determining region 3 of an antibody heavy chain (CDR-H3) has a major impact on the antigenic specificity of an antibody. We used next-generation sequencing to characterize the CDR-H3 sequences in paired siblings of 4 families in which only one member of each pair had chronic HBV infection. Blood samples were obtained before and 2 weeks after HBV</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 May</publication><modification>2026-05-30T08:48:55.084Z</modification><creation>2019-03-27T02:14:30Z</creation></dates><accession>S-EPMC4879636</accession><cross_references><pubmed>27222149</pubmed><doi>10.1038/srep26556</doi></cross_references></HashMap>