The TNF superfamily in 2009: new pathways, new indications, and new drugs

Today's most successful class of biologics targets the inflammatory cytokine tumor necrosis factor in autoimmune diseases including rheumatoid arthritis, psoriasis and Crohn's. With five anti-TNF biologics now on the market, attention has turned toward novel strategies to improve the safet...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Drug discovery today 2009-12, Vol.14 (23-24), p.1082-1088
Hauptverfasser: Tansey, Malú G., Szymkowski, David E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1088
container_issue 23-24
container_start_page 1082
container_title Drug discovery today
container_volume 14
creator Tansey, Malú G.
Szymkowski, David E.
description Today's most successful class of biologics targets the inflammatory cytokine tumor necrosis factor in autoimmune diseases including rheumatoid arthritis, psoriasis and Crohn's. With five anti-TNF biologics now on the market, attention has turned toward novel strategies to improve the safety and efficacy of next-generation TNF inhibitors. Beyond TNF, drugs are under development that modulate many other ligands and receptors of the TNF superfamily. Biologics targeting at least 16 of the approximately 22 known ligand–receptor pairs are now in clinical development for autoimmune diseases, cancers and osteoporosis. A deeper understanding of intracellular signaling has also facilitated small-molecule interventions, opening the door to oral therapies. This report summarizes recent developments in this highly druggable superfamily, including highlights of the latest international TNF conference.
doi_str_mv 10.1016/j.drudis.2009.10.002
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_877571736</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1359644609003377</els_id><sourcerecordid>733785286</sourcerecordid><originalsourceid>FETCH-LOGICAL-c457t-4bb09ef91085f872e048fb05040405a329c967971857055b7d33299e481be0e13</originalsourceid><addsrcrecordid>eNqNkcFPwjAUxhujEUT_A2N28-KwXdu19WBiiCgJ0Quem257kxLYsN0k_Pd2QOJNSQ9tv_ze-17eh9A1wUOCSXq_GBauLawfJhirIA0xTk5Qn0ghYy5pchrelKs4ZSztoQvvFxiTRPH0HPWIklQQmfbRZDaHaPY2jny7BlealV1uI1tFXdOHqIJNtDbNfGO2_m73s1Vhc9PYugqCqYqdGAb59JforDRLD1eHe4A-xs-z0Ws8fX-ZjJ6mcc64aGKWZVhBqQiWvJQiAcxkmWGOWTjc0ETlKhUqTMcF5jwTBQ2aAiZJBhgIHaDbfd-1q79a8I1eWZ_DcmkqqFuvpRBcEEHTo8hUMUWPJAlj_5KCUiF5Ijt3tidzV3vvoNRrZ1fGbTXBuktQL_Q-Qd0tu1NDgqHs5mDQZisofosOkQXgcQ9AWPK3Bad9bqHKobAO8kYXtf3b4QdfH6og</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733785286</pqid></control><display><type>article</type><title>The TNF superfamily in 2009: new pathways, new indications, and new drugs</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Tansey, Malú G. ; Szymkowski, David E.</creator><creatorcontrib>Tansey, Malú G. ; Szymkowski, David E.</creatorcontrib><description>Today's most successful class of biologics targets the inflammatory cytokine tumor necrosis factor in autoimmune diseases including rheumatoid arthritis, psoriasis and Crohn's. With five anti-TNF biologics now on the market, attention has turned toward novel strategies to improve the safety and efficacy of next-generation TNF inhibitors. Beyond TNF, drugs are under development that modulate many other ligands and receptors of the TNF superfamily. Biologics targeting at least 16 of the approximately 22 known ligand–receptor pairs are now in clinical development for autoimmune diseases, cancers and osteoporosis. A deeper understanding of intracellular signaling has also facilitated small-molecule interventions, opening the door to oral therapies. This report summarizes recent developments in this highly druggable superfamily, including highlights of the latest international TNF conference.</description><identifier>ISSN: 1359-6446</identifier><identifier>EISSN: 1878-5832</identifier><identifier>DOI: 10.1016/j.drudis.2009.10.002</identifier><identifier>PMID: 19837186</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Autoimmune Diseases - drug therapy ; Autoimmune Diseases - immunology ; Autoimmune Diseases - metabolism ; Drug Discovery ; Humans ; Neoplasms - drug therapy ; Neoplasms - immunology ; Neoplasms - metabolism ; Osteoporosis - drug therapy ; Osteoporosis - immunology ; Osteoporosis - metabolism ; Tumor Necrosis Factors - antagonists &amp; inhibitors ; Tumor Necrosis Factors - physiology</subject><ispartof>Drug discovery today, 2009-12, Vol.14 (23-24), p.1082-1088</ispartof><rights>2009 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-4bb09ef91085f872e048fb05040405a329c967971857055b7d33299e481be0e13</citedby><cites>FETCH-LOGICAL-c457t-4bb09ef91085f872e048fb05040405a329c967971857055b7d33299e481be0e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.drudis.2009.10.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>310,311,315,781,785,790,791,3551,23932,23933,25142,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19837186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tansey, Malú G.</creatorcontrib><creatorcontrib>Szymkowski, David E.</creatorcontrib><title>The TNF superfamily in 2009: new pathways, new indications, and new drugs</title><title>Drug discovery today</title><addtitle>Drug Discov Today</addtitle><description>Today's most successful class of biologics targets the inflammatory cytokine tumor necrosis factor in autoimmune diseases including rheumatoid arthritis, psoriasis and Crohn's. With five anti-TNF biologics now on the market, attention has turned toward novel strategies to improve the safety and efficacy of next-generation TNF inhibitors. Beyond TNF, drugs are under development that modulate many other ligands and receptors of the TNF superfamily. Biologics targeting at least 16 of the approximately 22 known ligand–receptor pairs are now in clinical development for autoimmune diseases, cancers and osteoporosis. A deeper understanding of intracellular signaling has also facilitated small-molecule interventions, opening the door to oral therapies. This report summarizes recent developments in this highly druggable superfamily, including highlights of the latest international TNF conference.</description><subject>Autoimmune Diseases - drug therapy</subject><subject>Autoimmune Diseases - immunology</subject><subject>Autoimmune Diseases - metabolism</subject><subject>Drug Discovery</subject><subject>Humans</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - metabolism</subject><subject>Osteoporosis - drug therapy</subject><subject>Osteoporosis - immunology</subject><subject>Osteoporosis - metabolism</subject><subject>Tumor Necrosis Factors - antagonists &amp; inhibitors</subject><subject>Tumor Necrosis Factors - physiology</subject><issn>1359-6446</issn><issn>1878-5832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFPwjAUxhujEUT_A2N28-KwXdu19WBiiCgJ0Quem257kxLYsN0k_Pd2QOJNSQ9tv_ze-17eh9A1wUOCSXq_GBauLawfJhirIA0xTk5Qn0ghYy5pchrelKs4ZSztoQvvFxiTRPH0HPWIklQQmfbRZDaHaPY2jny7BlealV1uI1tFXdOHqIJNtDbNfGO2_m73s1Vhc9PYugqCqYqdGAb59JforDRLD1eHe4A-xs-z0Ws8fX-ZjJ6mcc64aGKWZVhBqQiWvJQiAcxkmWGOWTjc0ETlKhUqTMcF5jwTBQ2aAiZJBhgIHaDbfd-1q79a8I1eWZ_DcmkqqFuvpRBcEEHTo8hUMUWPJAlj_5KCUiF5Ijt3tidzV3vvoNRrZ1fGbTXBuktQL_Q-Qd0tu1NDgqHs5mDQZisofosOkQXgcQ9AWPK3Bad9bqHKobAO8kYXtf3b4QdfH6og</recordid><startdate>200912</startdate><enddate>200912</enddate><creator>Tansey, Malú G.</creator><creator>Szymkowski, David E.</creator><general>Elsevier Ltd</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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>200912</creationdate><title>The TNF superfamily in 2009: new pathways, new indications, and new drugs</title><author>Tansey, Malú G. ; Szymkowski, David E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-4bb09ef91085f872e048fb05040405a329c967971857055b7d33299e481be0e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Autoimmune Diseases - drug therapy</topic><topic>Autoimmune Diseases - immunology</topic><topic>Autoimmune Diseases - metabolism</topic><topic>Drug Discovery</topic><topic>Humans</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - metabolism</topic><topic>Osteoporosis - drug therapy</topic><topic>Osteoporosis - immunology</topic><topic>Osteoporosis - metabolism</topic><topic>Tumor Necrosis Factors - antagonists &amp; inhibitors</topic><topic>Tumor Necrosis Factors - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tansey, Malú G.</creatorcontrib><creatorcontrib>Szymkowski, David E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Drug discovery today</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tansey, Malú G.</au><au>Szymkowski, David E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The TNF superfamily in 2009: new pathways, new indications, and new drugs</atitle><jtitle>Drug discovery today</jtitle><addtitle>Drug Discov Today</addtitle><date>2009-12</date><risdate>2009</risdate><volume>14</volume><issue>23-24</issue><spage>1082</spage><epage>1088</epage><pages>1082-1088</pages><issn>1359-6446</issn><eissn>1878-5832</eissn><abstract>Today's most successful class of biologics targets the inflammatory cytokine tumor necrosis factor in autoimmune diseases including rheumatoid arthritis, psoriasis and Crohn's. With five anti-TNF biologics now on the market, attention has turned toward novel strategies to improve the safety and efficacy of next-generation TNF inhibitors. Beyond TNF, drugs are under development that modulate many other ligands and receptors of the TNF superfamily. Biologics targeting at least 16 of the approximately 22 known ligand–receptor pairs are now in clinical development for autoimmune diseases, cancers and osteoporosis. A deeper understanding of intracellular signaling has also facilitated small-molecule interventions, opening the door to oral therapies. This report summarizes recent developments in this highly druggable superfamily, including highlights of the latest international TNF conference.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19837186</pmid><doi>10.1016/j.drudis.2009.10.002</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1359-6446
ispartof Drug discovery today, 2009-12, Vol.14 (23-24), p.1082-1088
issn 1359-6446
1878-5832
language eng
recordid cdi_proquest_miscellaneous_877571736
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Autoimmune Diseases - drug therapy
Autoimmune Diseases - immunology
Autoimmune Diseases - metabolism
Drug Discovery
Humans
Neoplasms - drug therapy
Neoplasms - immunology
Neoplasms - metabolism
Osteoporosis - drug therapy
Osteoporosis - immunology
Osteoporosis - metabolism
Tumor Necrosis Factors - antagonists & inhibitors
Tumor Necrosis Factors - physiology
title The TNF superfamily in 2009: new pathways, new indications, and new drugs
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T02%3A16%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20TNF%20superfamily%20in%202009:%20new%20pathways,%20new%20indications,%20and%20new%20drugs&rft.jtitle=Drug%20discovery%20today&rft.au=Tansey,%20Mal%C3%BA%20G.&rft.date=2009-12&rft.volume=14&rft.issue=23-24&rft.spage=1082&rft.epage=1088&rft.pages=1082-1088&rft.issn=1359-6446&rft.eissn=1878-5832&rft_id=info:doi/10.1016/j.drudis.2009.10.002&rft_dat=%3Cproquest_cross%3E733785286%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733785286&rft_id=info:pmid/19837186&rft_els_id=S1359644609003377&rfr_iscdi=true