<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ahmed M</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>eaay0233</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7354419</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(528)</volume><pubmed_abstract>One quarter of the world's population is infected with &lt;i>Mycobacterium tuberculosis&lt;/i> (&lt;i>Mtb&lt;/i>), the causative agent of tuberculosis (TB). Although most infected individuals successfully control or clear the infection, some individuals will progress to TB disease. Immune correlates identified using animal models are not always effectively translated to human TB, thus resulting in a slow pace of translational discoveries from animal models to human TB for many platforms including vaccines, therapeutics, biomarkers, and diagnostic discovery. Therefore, it is critical to improve our poor understanding of immune correlates of disease and protection that are shared across animal TB models and human TB. In this study, we have provided an in-depth identification of the conserved and diversi</pubmed_abstract><journal>Science translational medicine</journal><pubmed_title>Immune correlates of tuberculosis disease and risk translate across species.</pubmed_title><pmcid>PMC7354419</pmcid><funding_grant_id>P51 OD011104</funding_grant_id><funding_grant_id>R01 AI111943</funding_grant_id><funding_grant_id>R01 AI134236</funding_grant_id><funding_grant_id>P51 OD011133</funding_grant_id><funding_grant_id>AI111914-02</funding_grant_id><funding_grant_id>U42 OD010442</funding_grant_id><funding_grant_id>AI123780</funding_grant_id><funding_grant_id>HL105427</funding_grant_id><funding_grant_id>AI134236-02</funding_grant_id><funding_grant_id>U19 AI091036</funding_grant_id><funding_grant_id>R01 HL105427</funding_grant_id><funding_grant_id>R01 AI123780</funding_grant_id><funding_grant_id>U19 AI106772</funding_grant_id><funding_grant_id>R01 AI111914</funding_grant_id><pubmed_authors>Diamond MS</pubmed_authors><pubmed_authors>Means T</pubmed_authors><pubmed_authors>Das S</pubmed_authors><pubmed_authors>Khader SA</pubmed_authors><pubmed_authors>Ahmed M</pubmed_authors><pubmed_authors>Rangel-Moreno J</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Mitreva M</pubmed_authors><pubmed_authors>Thirunavukkarasu S</pubmed_authors><pubmed_authors>Thackray LB</pubmed_authors><pubmed_authors>Martin J</pubmed_authors><pubmed_authors>Scriba TJ</pubmed_authors><pubmed_authors>Mehra S</pubmed_authors><pubmed_authors>Mbandi SK</pubmed_authors><pubmed_authors>Thomas KA</pubmed_authors><pubmed_authors>Rosa BA</pubmed_authors><pubmed_authors>Murphy KM</pubmed_authors><pubmed_authors>Kaushal D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune correlates of tuberculosis disease and risk translate across species.</name><description>One quarter of the world's population is infected with &lt;i>Mycobacterium tuberculosis&lt;/i> (&lt;i>Mtb&lt;/i>), the causative agent of tuberculosis (TB). Although most infected individuals successfully control or clear the infection, some individuals will progress to TB disease. Immune correlates identified using animal models are not always effectively translated to human TB, thus resulting in a slow pace of translational discoveries from animal models to human TB for many platforms including vaccines, therapeutics, biomarkers, and diagnostic discovery. Therefore, it is critical to improve our poor understanding of immune correlates of disease and protection that are shared across animal TB models and human TB. In this study, we have provided an in-depth identification of the conserved and diversi</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2026-05-03T22:19:03.798Z</modification><creation>2020-10-29T14:49:50Z</creation></dates><accession>S-EPMC7354419</accession><cross_references><pubmed>31996462</pubmed><doi>10.1126/scitranslmed.aay0233</doi></cross_references></HashMap>