<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Oseroff C</submitter><funding>NIAID NIH HHS</funding><pagination>1800-11</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3411923</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>189(4)</volume><pubmed_abstract>A panel of 133 allergens derived from 28 different sources, including fungi, trees, grasses, weeds, and indoor allergens, was surveyed utilizing prediction of HLA class II-binding peptides and ELISPOT assays with PBMC from allergic donors, resulting in the identification of 257 T cell epitopes. More than 90% of the epitopes were novel, and for 14 allergen sources were the first ever identified to our knowledge. The epitopes identified in the different allergen sources summed up to a variable fraction of the total extract response. In cases of allergens in which the identified T cell epitopes accounted for a minor fraction of the extract response, fewer known protein sequences were available, suggesting that for low epitope coverage allergen sources, additional allergen proteins remain to b</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>T cell responses to known allergen proteins are differently polarized and account for a variable fraction of total response to allergen extracts.</pubmed_title><pmcid>PMC3411923</pmcid><funding_grant_id>U19AI100275</funding_grant_id><funding_grant_id>N01 AI040023</funding_grant_id><funding_grant_id>R37 AI038425</funding_grant_id><funding_grant_id>R01 AI091614</funding_grant_id><funding_grant_id>U19 AI100275</funding_grant_id><pubmed_authors>McKinney DM</pubmed_authors><pubmed_authors>Brodie TM</pubmed_authors><pubmed_authors>Sallusto F</pubmed_authors><pubmed_authors>Alam R</pubmed_authors><pubmed_authors>Peters B</pubmed_authors><pubmed_authors>Sette A</pubmed_authors><pubmed_authors>Sidney J</pubmed_authors><pubmed_authors>Vita R</pubmed_authors><pubmed_authors>Oseroff C</pubmed_authors><pubmed_authors>Kolla R</pubmed_authors><pubmed_authors>Southwood S</pubmed_authors><pubmed_authors>Grey H</pubmed_authors><pubmed_authors>Broide D</pubmed_authors><pubmed_authors>Tripple V</pubmed_authors><pubmed_authors>Greenbaum JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>T cell responses to known allergen proteins are differently polarized and account for a variable fraction of total response to allergen extracts.</name><description>A panel of 133 allergens derived from 28 different sources, including fungi, trees, grasses, weeds, and indoor allergens, was surveyed utilizing prediction of HLA class II-binding peptides and ELISPOT assays with PBMC from allergic donors, resulting in the identification of 257 T cell epitopes. More than 90% of the epitopes were novel, and for 14 allergen sources were the first ever identified to our knowledge. The epitopes identified in the different allergen sources summed up to a variable fraction of the total extract response. In cases of allergens in which the identified T cell epitopes accounted for a minor fraction of the extract response, fewer known protein sequences were available, suggesting that for low epitope coverage allergen sources, additional allergen proteins remain to b</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Aug</publication><modification>2025-04-22T07:45:38.587Z</modification><creation>2019-03-26T23:42:57Z</creation></dates><accession>S-EPMC3411923</accession><cross_references><pubmed>22786768</pubmed><doi>10.4049/jimmunol.1200850</doi></cross_references></HashMap>