<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Paschold L</submitter><funding>Deutsche Krebshilfe</funding><funding>Martin-Luther-Universität Halle-Wittenberg</funding><pagination>9516</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10258752</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>We set out to gain insight into peripheral blood B and T cell repertoires from 120 infants of the LoewenKIDS birth cohort to investigate potential determinants of early life respiratory infections. Low antigen-dependent somatic hypermutation of B cell repertoires, as well as low T and B cell repertoire clonality, high diversity, and high richness especially in public T cell clonotypes reflected the immunological naivety at 12 months of age when high thymic and bone marrow output are associated with relatively few prior antigen encounters. Infants with inadequately low T cell repertoire diversity or high clonality showed higher numbers of acute respiratory infections over the first 4 years of life. No correlation of T or B cell repertoire metrics with other parameters such as sex, birth mod</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>T cell repertoire breadth is associated with the number of acute respiratory infections in the LoewenKIDS birth cohort.</pubmed_title><pmcid>PMC10258752</pmcid><funding_grant_id>70114663</funding_grant_id><pubmed_authors>Riese P</pubmed_authors><pubmed_authors>Trittel S</pubmed_authors><pubmed_authors>Schultheiß C</pubmed_authors><pubmed_authors>Mikolajczyk R</pubmed_authors><pubmed_authors>Langer S</pubmed_authors><pubmed_authors>Strowig T</pubmed_authors><pubmed_authors>Gottschick C</pubmed_authors><pubmed_authors>Paschold L</pubmed_authors><pubmed_authors>Eberl W</pubmed_authors><pubmed_authors>Dressler F</pubmed_authors><pubmed_authors>Hubner J</pubmed_authors><pubmed_authors>Guzman CA</pubmed_authors><pubmed_authors>Binder M</pubmed_authors><pubmed_authors>Diexer S</pubmed_authors><pubmed_authors>Purschke O</pubmed_authors><pubmed_authors>Aksentijevich I</pubmed_authors><pubmed_authors>Klee B</pubmed_authors><pubmed_authors>Haase R</pubmed_authors></additional><is_claimable>false</is_claimable><name>T cell repertoire breadth is associated with the number of acute respiratory infections in the LoewenKIDS birth cohort.</name><description>We set out to gain insight into peripheral blood B and T cell repertoires from 120 infants of the LoewenKIDS birth cohort to investigate potential determinants of early life respiratory infections. Low antigen-dependent somatic hypermutation of B cell repertoires, as well as low T and B cell repertoire clonality, high diversity, and high richness especially in public T cell clonotypes reflected the immunological naivety at 12 months of age when high thymic and bone marrow output are associated with relatively few prior antigen encounters. Infants with inadequately low T cell repertoire diversity or high clonality showed higher numbers of acute respiratory infections over the first 4 years of life. No correlation of T or B cell repertoire metrics with other parameters such as sex, birth mod</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-05-29T01:14:39.668Z</modification><creation>2024-12-03T19:33:25.488Z</creation></dates><accession>S-EPMC10258752</accession><cross_references><pubmed>37308563</pubmed><doi>10.1038/s41598-023-36144-x</doi></cross_references></HashMap>