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Use of a Contained Mycobacterium tuberculosis Mouse Infection Model to Predict Active Disease and Containment in Humans
Abstract Previous studies have identified whole-blood transcriptional risk and disease signatures for tuberculosis; however, several lines of evidence suggest that these signatures primarily reflect bacterial burden, which increases before symptomatic disease. We found that the peripheral blood tran...
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Published in: | The Journal of infectious diseases 2022-05, Vol.225 (10), p.1832-1840 |
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creator | Duffy, Fergal J Olson, Gregory S Gold, Elizabeth S Jahn, Ana Aderem, Alan Aitchison, John D Rothchild, Alissa C Diercks, Alan H Nemeth, Johannes |
description | Abstract
Previous studies have identified whole-blood transcriptional risk and disease signatures for tuberculosis; however, several lines of evidence suggest that these signatures primarily reflect bacterial burden, which increases before symptomatic disease. We found that the peripheral blood transcriptome of mice with contained Mycobacterium tuberculosis infection (CMTI) has striking similarities to that of humans with active tuberculosis and that a signature derived from these mice predicts human disease with accuracy comparable to that of signatures derived directly from humans. A set of genes associated with immune defense are up-regulated in mice with CMTI but not in humans with active tuberculosis, suggesting that their up-regulation is associated with bacterial containment. A signature comprising these genes predicts both protection from tuberculosis disease and successful treatment at early time points where current signatures are not predictive. These results suggest that detailed study of the CMTI model may enable identification of biomarkers for human tuberculosis.
We previously described the mouse contained tuberculosis model, which protects mice against aerosol challenge. Here we show that blood RNA signatures derived from this model correlate with disease and tuberculosis containment in multiple human cohorts. |
doi_str_mv | 10.1093/infdis/jiab130 |
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Previous studies have identified whole-blood transcriptional risk and disease signatures for tuberculosis; however, several lines of evidence suggest that these signatures primarily reflect bacterial burden, which increases before symptomatic disease. We found that the peripheral blood transcriptome of mice with contained Mycobacterium tuberculosis infection (CMTI) has striking similarities to that of humans with active tuberculosis and that a signature derived from these mice predicts human disease with accuracy comparable to that of signatures derived directly from humans. A set of genes associated with immune defense are up-regulated in mice with CMTI but not in humans with active tuberculosis, suggesting that their up-regulation is associated with bacterial containment. A signature comprising these genes predicts both protection from tuberculosis disease and successful treatment at early time points where current signatures are not predictive. These results suggest that detailed study of the CMTI model may enable identification of biomarkers for human tuberculosis.
We previously described the mouse contained tuberculosis model, which protects mice against aerosol challenge. Here we show that blood RNA signatures derived from this model correlate with disease and tuberculosis containment in multiple human cohorts.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiab130</identifier><identifier>PMID: 33693706</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Animals ; Biomarkers ; Humans ; Immune system ; Major and Brief Reports ; Mice ; Mycobacterium tuberculosis ; Peripheral blood ; Rodents ; Transcriptome ; Transcriptomes ; Tuberculosis</subject><ispartof>The Journal of infectious diseases, 2022-05, Vol.225 (10), p.1832-1840</ispartof><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-88dfae8ecc468025a9e0a282cccd5810673dc7a31218d0901cc5e37b206a9a893</citedby><cites>FETCH-LOGICAL-c452t-88dfae8ecc468025a9e0a282cccd5810673dc7a31218d0901cc5e37b206a9a893</cites><orcidid>0000-0002-9153-6497 ; 0000-0002-4675-0937</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33693706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duffy, Fergal J</creatorcontrib><creatorcontrib>Olson, Gregory S</creatorcontrib><creatorcontrib>Gold, Elizabeth S</creatorcontrib><creatorcontrib>Jahn, Ana</creatorcontrib><creatorcontrib>Aderem, Alan</creatorcontrib><creatorcontrib>Aitchison, John D</creatorcontrib><creatorcontrib>Rothchild, Alissa C</creatorcontrib><creatorcontrib>Diercks, Alan H</creatorcontrib><creatorcontrib>Nemeth, Johannes</creatorcontrib><title>Use of a Contained Mycobacterium tuberculosis Mouse Infection Model to Predict Active Disease and Containment in Humans</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Abstract
Previous studies have identified whole-blood transcriptional risk and disease signatures for tuberculosis; however, several lines of evidence suggest that these signatures primarily reflect bacterial burden, which increases before symptomatic disease. We found that the peripheral blood transcriptome of mice with contained Mycobacterium tuberculosis infection (CMTI) has striking similarities to that of humans with active tuberculosis and that a signature derived from these mice predicts human disease with accuracy comparable to that of signatures derived directly from humans. A set of genes associated with immune defense are up-regulated in mice with CMTI but not in humans with active tuberculosis, suggesting that their up-regulation is associated with bacterial containment. A signature comprising these genes predicts both protection from tuberculosis disease and successful treatment at early time points where current signatures are not predictive. These results suggest that detailed study of the CMTI model may enable identification of biomarkers for human tuberculosis.
We previously described the mouse contained tuberculosis model, which protects mice against aerosol challenge. Here we show that blood RNA signatures derived from this model correlate with disease and tuberculosis containment in multiple human cohorts.</description><subject>Animals</subject><subject>Biomarkers</subject><subject>Humans</subject><subject>Immune system</subject><subject>Major and Brief Reports</subject><subject>Mice</subject><subject>Mycobacterium tuberculosis</subject><subject>Peripheral blood</subject><subject>Rodents</subject><subject>Transcriptome</subject><subject>Transcriptomes</subject><subject>Tuberculosis</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqFkc9vFCEUx4nR2G316tGQeLGHaR-wA8zFpFl_tEkbPdgzYeCNspmBFWZq-t-L2W2jXjwReB8-ee99CXnF4IxBJ85DHHwo59tgeybgCVmxVqhGSiaekhUA5w3TXXdEjkvZAsBaSPWcHAkhO6FArsjP24I0DdTSTYqzDRE9vbl3qbduxhyWic5Lj9ktYyqh0Ju0VP4qDujmkGK9exzpnOiXjD64mV7U9zuk70NBW0kb_YN4wjjTEOnlMtlYXpBngx0LvjycJ-T244evm8vm-vOnq83FdePWLZ8brf1gUaNza6mBt7ZDsFxz55xvNQOphHfKCsaZ9tABc65FoXoO0nZWd-KEvNt7d0s_oXe1iWxHs8thsvneJBvM35UYvptv6c50jIm1klXw9iDI6ceCZTZTKA7H0UasyzC8BRBKgFxX9M0_6DYtOdbxDJeq1a1WoCp1tqdcTqVkHB6bYWB-Z2r2mZpDpvXD6z9HeMQfQqzA6R5Iy-5_sl-pmq9M</recordid><startdate>20220516</startdate><enddate>20220516</enddate><creator>Duffy, Fergal J</creator><creator>Olson, Gregory S</creator><creator>Gold, Elizabeth S</creator><creator>Jahn, Ana</creator><creator>Aderem, Alan</creator><creator>Aitchison, John D</creator><creator>Rothchild, Alissa C</creator><creator>Diercks, Alan H</creator><creator>Nemeth, Johannes</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9153-6497</orcidid><orcidid>https://orcid.org/0000-0002-4675-0937</orcidid></search><sort><creationdate>20220516</creationdate><title>Use of a Contained Mycobacterium tuberculosis Mouse Infection Model to Predict Active Disease and Containment in Humans</title><author>Duffy, Fergal J ; Olson, Gregory S ; Gold, Elizabeth S ; Jahn, Ana ; Aderem, Alan ; Aitchison, John D ; Rothchild, Alissa C ; Diercks, Alan H ; Nemeth, Johannes</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-88dfae8ecc468025a9e0a282cccd5810673dc7a31218d0901cc5e37b206a9a893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Biomarkers</topic><topic>Humans</topic><topic>Immune system</topic><topic>Major and Brief Reports</topic><topic>Mice</topic><topic>Mycobacterium tuberculosis</topic><topic>Peripheral blood</topic><topic>Rodents</topic><topic>Transcriptome</topic><topic>Transcriptomes</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duffy, Fergal J</creatorcontrib><creatorcontrib>Olson, Gregory S</creatorcontrib><creatorcontrib>Gold, Elizabeth S</creatorcontrib><creatorcontrib>Jahn, Ana</creatorcontrib><creatorcontrib>Aderem, Alan</creatorcontrib><creatorcontrib>Aitchison, John D</creatorcontrib><creatorcontrib>Rothchild, Alissa C</creatorcontrib><creatorcontrib>Diercks, Alan H</creatorcontrib><creatorcontrib>Nemeth, Johannes</creatorcontrib><collection>Oxford University Press Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duffy, Fergal J</au><au>Olson, Gregory S</au><au>Gold, Elizabeth S</au><au>Jahn, Ana</au><au>Aderem, Alan</au><au>Aitchison, John D</au><au>Rothchild, Alissa C</au><au>Diercks, Alan H</au><au>Nemeth, Johannes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of a Contained Mycobacterium tuberculosis Mouse Infection Model to Predict Active Disease and Containment in Humans</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2022-05-16</date><risdate>2022</risdate><volume>225</volume><issue>10</issue><spage>1832</spage><epage>1840</epage><pages>1832-1840</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Abstract
Previous studies have identified whole-blood transcriptional risk and disease signatures for tuberculosis; however, several lines of evidence suggest that these signatures primarily reflect bacterial burden, which increases before symptomatic disease. We found that the peripheral blood transcriptome of mice with contained Mycobacterium tuberculosis infection (CMTI) has striking similarities to that of humans with active tuberculosis and that a signature derived from these mice predicts human disease with accuracy comparable to that of signatures derived directly from humans. A set of genes associated with immune defense are up-regulated in mice with CMTI but not in humans with active tuberculosis, suggesting that their up-regulation is associated with bacterial containment. A signature comprising these genes predicts both protection from tuberculosis disease and successful treatment at early time points where current signatures are not predictive. These results suggest that detailed study of the CMTI model may enable identification of biomarkers for human tuberculosis.
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subjects | Animals Biomarkers Humans Immune system Major and Brief Reports Mice Mycobacterium tuberculosis Peripheral blood Rodents Transcriptome Transcriptomes Tuberculosis |
title | Use of a Contained Mycobacterium tuberculosis Mouse Infection Model to Predict Active Disease and Containment in Humans |
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