Harnessing regulatory T cells to suppress asthma: from potential to therapy
Regulatory T cells (Tregs) play an essential role in maintaining the homeostatic balance of immune responses. Asthma is an inflammatory condition of the airways that is driven by dysregulated immune responses toward normally innocuous antigens. Individuals with asthma have fewer and less functional...
Gespeichert in:
Veröffentlicht in: | American journal of respiratory cell and molecular biology 2010-11, Vol.43 (5), p.511-519 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 519 |
---|---|
container_issue | 5 |
container_start_page | 511 |
container_title | American journal of respiratory cell and molecular biology |
container_volume | 43 |
creator | Thorburn, Alison N Hansbro, Philip M |
description | Regulatory T cells (Tregs) play an essential role in maintaining the homeostatic balance of immune responses. Asthma is an inflammatory condition of the airways that is driven by dysregulated immune responses toward normally innocuous antigens. Individuals with asthma have fewer and less functional Tregs, which may lead to uncontrolled effector cell responses and promote proasthmatic responses of T helper type 2, T helper 17, natural killer T, antigen-presenting, and B cells. Tregs have the capacity to either directly or indirectly suppress these responses. Hence, the induced expansion of functional Tregs in predisposed or individuals with asthma is a potential approach for the prevention and treatment of asthma. Infection by a number of micro-organisms has been associated with reduced prevalence of asthma, and many infectious agents have been shown to induce Tregs and reduce allergic airways disease in mouse models. The translation of the regulatory and therapeutic properties of infectious agents for use in asthma requires the identification of key modulatory components and the development and trial of effective immunoregulatory therapies. Further translational and clinical research is required for the induction of Tregs to be harnessed as a therapeutic strategy for asthma. |
doi_str_mv | 10.1165/rcmb.2009-0342TR |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2970851</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>760154488</sourcerecordid><originalsourceid>FETCH-LOGICAL-c333t-6dd56cf3dd660b7904a24db590479e629e98071ff146a7e248da201c72ed73623</originalsourceid><addsrcrecordid>eNpdkUtLxDAUhYMoPkb3rqS4cVW9eTRpXAgivnBAkHEdMm0606FtapIK8-9NmVHUVS7kO4d77kHoFMMlxjy7ckU7vyQAMgXKyOxtBx3ijGYpk7ncjTMwluKMyQN05P0KAJMc4310MEpETuEQvTxp1xnv626ROLMYGh2sWyezpDBN45NgEz_0vYtEon1Ytvo6qZxtk94G04VaNyMSlsbpfn2M9irdeHOyfSfo_eF-dveUTl8fn-9up2lBKQ0pL8uMFxUtS85hLiQwTVg5z-IgpOFEGpmDwFWFGdfCEJaXmgAuBDGloJzQCbrZ-PbDvDVlERdxulG9q1vt1srqWv396eqlWthPRaSAPMPR4GJr4OzHYHxQbe3HwLozdvBKcIhXY3keyfN_5MoOrovpIkQIphx4hGADFc5670z1swoGNfakxp7UeHS16SlKzn5H-BF8F0O_AGQPj-U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>762213606</pqid></control><display><type>article</type><title>Harnessing regulatory T cells to suppress asthma: from potential to therapy</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><source>Journals@Ovid Complete</source><creator>Thorburn, Alison N ; Hansbro, Philip M</creator><creatorcontrib>Thorburn, Alison N ; Hansbro, Philip M</creatorcontrib><description>Regulatory T cells (Tregs) play an essential role in maintaining the homeostatic balance of immune responses. Asthma is an inflammatory condition of the airways that is driven by dysregulated immune responses toward normally innocuous antigens. Individuals with asthma have fewer and less functional Tregs, which may lead to uncontrolled effector cell responses and promote proasthmatic responses of T helper type 2, T helper 17, natural killer T, antigen-presenting, and B cells. Tregs have the capacity to either directly or indirectly suppress these responses. Hence, the induced expansion of functional Tregs in predisposed or individuals with asthma is a potential approach for the prevention and treatment of asthma. Infection by a number of micro-organisms has been associated with reduced prevalence of asthma, and many infectious agents have been shown to induce Tregs and reduce allergic airways disease in mouse models. The translation of the regulatory and therapeutic properties of infectious agents for use in asthma requires the identification of key modulatory components and the development and trial of effective immunoregulatory therapies. Further translational and clinical research is required for the induction of Tregs to be harnessed as a therapeutic strategy for asthma.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/rcmb.2009-0342TR</identifier><identifier>PMID: 20097830</identifier><identifier>CODEN: AJRBEL</identifier><language>eng</language><publisher>United States: American Thoracic Society</publisher><subject>Animals ; Asthma - immunology ; Asthma - therapy ; Biomarkers ; Humans ; Immune Tolerance - immunology ; T-Lymphocytes, Regulatory - immunology ; Translational Reviews</subject><ispartof>American journal of respiratory cell and molecular biology, 2010-11, Vol.43 (5), p.511-519</ispartof><rights>Copyright American Thoracic Society Nov 2010</rights><rights>Copyright © 2010, American Thoracic Society 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c333t-6dd56cf3dd660b7904a24db590479e629e98071ff146a7e248da201c72ed73623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20097830$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thorburn, Alison N</creatorcontrib><creatorcontrib>Hansbro, Philip M</creatorcontrib><title>Harnessing regulatory T cells to suppress asthma: from potential to therapy</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>Regulatory T cells (Tregs) play an essential role in maintaining the homeostatic balance of immune responses. Asthma is an inflammatory condition of the airways that is driven by dysregulated immune responses toward normally innocuous antigens. Individuals with asthma have fewer and less functional Tregs, which may lead to uncontrolled effector cell responses and promote proasthmatic responses of T helper type 2, T helper 17, natural killer T, antigen-presenting, and B cells. Tregs have the capacity to either directly or indirectly suppress these responses. Hence, the induced expansion of functional Tregs in predisposed or individuals with asthma is a potential approach for the prevention and treatment of asthma. Infection by a number of micro-organisms has been associated with reduced prevalence of asthma, and many infectious agents have been shown to induce Tregs and reduce allergic airways disease in mouse models. The translation of the regulatory and therapeutic properties of infectious agents for use in asthma requires the identification of key modulatory components and the development and trial of effective immunoregulatory therapies. Further translational and clinical research is required for the induction of Tregs to be harnessed as a therapeutic strategy for asthma.</description><subject>Animals</subject><subject>Asthma - immunology</subject><subject>Asthma - therapy</subject><subject>Biomarkers</subject><subject>Humans</subject><subject>Immune Tolerance - immunology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Translational Reviews</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkUtLxDAUhYMoPkb3rqS4cVW9eTRpXAgivnBAkHEdMm0606FtapIK8-9NmVHUVS7kO4d77kHoFMMlxjy7ckU7vyQAMgXKyOxtBx3ijGYpk7ncjTMwluKMyQN05P0KAJMc4310MEpETuEQvTxp1xnv626ROLMYGh2sWyezpDBN45NgEz_0vYtEon1Ytvo6qZxtk94G04VaNyMSlsbpfn2M9irdeHOyfSfo_eF-dveUTl8fn-9up2lBKQ0pL8uMFxUtS85hLiQwTVg5z-IgpOFEGpmDwFWFGdfCEJaXmgAuBDGloJzQCbrZ-PbDvDVlERdxulG9q1vt1srqWv396eqlWthPRaSAPMPR4GJr4OzHYHxQbe3HwLozdvBKcIhXY3keyfN_5MoOrovpIkQIphx4hGADFc5670z1swoGNfakxp7UeHS16SlKzn5H-BF8F0O_AGQPj-U</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Thorburn, Alison N</creator><creator>Hansbro, Philip M</creator><general>American Thoracic Society</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20101101</creationdate><title>Harnessing regulatory T cells to suppress asthma: from potential to therapy</title><author>Thorburn, Alison N ; Hansbro, Philip M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-6dd56cf3dd660b7904a24db590479e629e98071ff146a7e248da201c72ed73623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Asthma - immunology</topic><topic>Asthma - therapy</topic><topic>Biomarkers</topic><topic>Humans</topic><topic>Immune Tolerance - immunology</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Translational Reviews</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thorburn, Alison N</creatorcontrib><creatorcontrib>Hansbro, Philip M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of respiratory cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thorburn, Alison N</au><au>Hansbro, Philip M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Harnessing regulatory T cells to suppress asthma: from potential to therapy</atitle><jtitle>American journal of respiratory cell and molecular biology</jtitle><addtitle>Am J Respir Cell Mol Biol</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>43</volume><issue>5</issue><spage>511</spage><epage>519</epage><pages>511-519</pages><issn>1044-1549</issn><eissn>1535-4989</eissn><coden>AJRBEL</coden><abstract>Regulatory T cells (Tregs) play an essential role in maintaining the homeostatic balance of immune responses. Asthma is an inflammatory condition of the airways that is driven by dysregulated immune responses toward normally innocuous antigens. Individuals with asthma have fewer and less functional Tregs, which may lead to uncontrolled effector cell responses and promote proasthmatic responses of T helper type 2, T helper 17, natural killer T, antigen-presenting, and B cells. Tregs have the capacity to either directly or indirectly suppress these responses. Hence, the induced expansion of functional Tregs in predisposed or individuals with asthma is a potential approach for the prevention and treatment of asthma. Infection by a number of micro-organisms has been associated with reduced prevalence of asthma, and many infectious agents have been shown to induce Tregs and reduce allergic airways disease in mouse models. The translation of the regulatory and therapeutic properties of infectious agents for use in asthma requires the identification of key modulatory components and the development and trial of effective immunoregulatory therapies. Further translational and clinical research is required for the induction of Tregs to be harnessed as a therapeutic strategy for asthma.</abstract><cop>United States</cop><pub>American Thoracic Society</pub><pmid>20097830</pmid><doi>10.1165/rcmb.2009-0342TR</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1044-1549 |
ispartof | American journal of respiratory cell and molecular biology, 2010-11, Vol.43 (5), p.511-519 |
issn | 1044-1549 1535-4989 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2970851 |
source | MEDLINE; Alma/SFX Local Collection; EZB Electronic Journals Library; Journals@Ovid Complete |
subjects | Animals Asthma - immunology Asthma - therapy Biomarkers Humans Immune Tolerance - immunology T-Lymphocytes, Regulatory - immunology Translational Reviews |
title | Harnessing regulatory T cells to suppress asthma: from potential to therapy |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T22%3A40%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Harnessing%20regulatory%20T%20cells%20to%20suppress%20asthma:%20from%20potential%20to%20therapy&rft.jtitle=American%20journal%20of%20respiratory%20cell%20and%20molecular%20biology&rft.au=Thorburn,%20Alison%20N&rft.date=2010-11-01&rft.volume=43&rft.issue=5&rft.spage=511&rft.epage=519&rft.pages=511-519&rft.issn=1044-1549&rft.eissn=1535-4989&rft.coden=AJRBEL&rft_id=info:doi/10.1165/rcmb.2009-0342TR&rft_dat=%3Cproquest_pubme%3E760154488%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=762213606&rft_id=info:pmid/20097830&rfr_iscdi=true |