Sequential immunotherapy: towards cures for autoimmunity

Despite major progress in the treatment of autoimmune diseases in the past two decades, most therapies do not cure disease and can be associated with increased risk of infection through broad suppression of the immune system. However, advances in understanding the causes of autoimmune disease and cl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature reviews. Drug discovery 2024-07, Vol.23 (7), p.501-524
Hauptverfasser: Ramírez-Valle, Francisco, Maranville, Joseph C., Roy, Sophie, Plenge, Robert M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 524
container_issue 7
container_start_page 501
container_title Nature reviews. Drug discovery
container_volume 23
creator Ramírez-Valle, Francisco
Maranville, Joseph C.
Roy, Sophie
Plenge, Robert M.
description Despite major progress in the treatment of autoimmune diseases in the past two decades, most therapies do not cure disease and can be associated with increased risk of infection through broad suppression of the immune system. However, advances in understanding the causes of autoimmune disease and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cell therapies provide evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. Here, we propose a ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal. This framework encompasses three steps: controlling inflammation; resetting the immune system through elimination of pathogenic immune memory cells; and promoting and maintaining immune homeostasis via immune regulatory agents and tissue repair. We discuss existing drugs and those in development for each of the three steps. We also highlight the importance of causal human biology in identifying and prioritizing novel immunotherapeutic strategies as well as informing their application in specific patient subsets, enabling precision medicine approaches that have the potential to transform clinical care. Advances in understanding of the cause of autoimmune diseases and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cells are providing evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. This article proposes a three-step ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal, and discusses existing drugs and those in development for each of the three steps.
doi_str_mv 10.1038/s41573-024-00959-8
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3065272455</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3065272455</sourcerecordid><originalsourceid>FETCH-LOGICAL-c256t-e7703c51dcf6a468c9afd8e4d39bb31ff6c27340bf3be30b1d7aae5fb8e38b203</originalsourceid><addsrcrecordid>eNp9kE1LxDAQhoMo7rr6BzxIwYuXaj6b1JssfsGCB_UckjTRLm2zJi2y_964XVfw4GkG5pl3hgeAUwQvESTiKlLEOMkhpjmEJStzsQemiHKaIy7o_q7nxQQcxbiEEBWI40MwIUKQskR4CsSz_Rhs19eqyeq2HTrfv9ugVuvrrPefKlQxM0OwMXM-ZGro_Qaq-_UxOHCqifZkW2fg9e72Zf6QL57uH-c3i9xgVvS55RwSw1BlXKFoIUypXCUsrUipNUHOFQZzQqF2RFsCNaq4UpY5LSwRGkMyAxdj7ir49GnsZVtHY5tGddYPURJYMMwxZSyh53_QpR9Cl75LFGcMMiJ4ovBImeBjDNbJVahbFdYSQfntVY5eZfIqN16lSEtn2-hBt7barfyITAAZgZhG3ZsNv7f_if0Cq-yDoQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3075505387</pqid></control><display><type>article</type><title>Sequential immunotherapy: towards cures for autoimmunity</title><source>Nature Journals Online</source><source>SpringerLink Journals - AutoHoldings</source><creator>Ramírez-Valle, Francisco ; Maranville, Joseph C. ; Roy, Sophie ; Plenge, Robert M.</creator><creatorcontrib>Ramírez-Valle, Francisco ; Maranville, Joseph C. ; Roy, Sophie ; Plenge, Robert M.</creatorcontrib><description>Despite major progress in the treatment of autoimmune diseases in the past two decades, most therapies do not cure disease and can be associated with increased risk of infection through broad suppression of the immune system. However, advances in understanding the causes of autoimmune disease and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cell therapies provide evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. Here, we propose a ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal. This framework encompasses three steps: controlling inflammation; resetting the immune system through elimination of pathogenic immune memory cells; and promoting and maintaining immune homeostasis via immune regulatory agents and tissue repair. We discuss existing drugs and those in development for each of the three steps. We also highlight the importance of causal human biology in identifying and prioritizing novel immunotherapeutic strategies as well as informing their application in specific patient subsets, enabling precision medicine approaches that have the potential to transform clinical care. Advances in understanding of the cause of autoimmune diseases and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cells are providing evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. This article proposes a three-step ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal, and discusses existing drugs and those in development for each of the three steps.</description><identifier>ISSN: 1474-1776</identifier><identifier>ISSN: 1474-1784</identifier><identifier>EISSN: 1474-1784</identifier><identifier>DOI: 10.1038/s41573-024-00959-8</identifier><identifier>PMID: 38839912</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/154 ; 631/250/38 ; Antigens ; Autoimmune diseases ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Cancer Research ; Homeostasis ; Immune system ; Immunotherapy ; Medicinal Chemistry ; Molecular Medicine ; Pharmacology/Toxicology ; Remission (Medicine) ; Review Article</subject><ispartof>Nature reviews. Drug discovery, 2024-07, Vol.23 (7), p.501-524</ispartof><rights>Springer Nature Limited 2024. corrected publication 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. Springer Nature Limited.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c256t-e7703c51dcf6a468c9afd8e4d39bb31ff6c27340bf3be30b1d7aae5fb8e38b203</cites><orcidid>0000-0002-1688-1573 ; 0000-0002-8625-5869</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41573-024-00959-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41573-024-00959-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38839912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramírez-Valle, Francisco</creatorcontrib><creatorcontrib>Maranville, Joseph C.</creatorcontrib><creatorcontrib>Roy, Sophie</creatorcontrib><creatorcontrib>Plenge, Robert M.</creatorcontrib><title>Sequential immunotherapy: towards cures for autoimmunity</title><title>Nature reviews. Drug discovery</title><addtitle>Nat Rev Drug Discov</addtitle><addtitle>Nat Rev Drug Discov</addtitle><description>Despite major progress in the treatment of autoimmune diseases in the past two decades, most therapies do not cure disease and can be associated with increased risk of infection through broad suppression of the immune system. However, advances in understanding the causes of autoimmune disease and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cell therapies provide evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. Here, we propose a ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal. This framework encompasses three steps: controlling inflammation; resetting the immune system through elimination of pathogenic immune memory cells; and promoting and maintaining immune homeostasis via immune regulatory agents and tissue repair. We discuss existing drugs and those in development for each of the three steps. We also highlight the importance of causal human biology in identifying and prioritizing novel immunotherapeutic strategies as well as informing their application in specific patient subsets, enabling precision medicine approaches that have the potential to transform clinical care. Advances in understanding of the cause of autoimmune diseases and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cells are providing evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. This article proposes a three-step ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal, and discusses existing drugs and those in development for each of the three steps.</description><subject>631/154</subject><subject>631/250/38</subject><subject>Antigens</subject><subject>Autoimmune diseases</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Cancer Research</subject><subject>Homeostasis</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>Medicinal Chemistry</subject><subject>Molecular Medicine</subject><subject>Pharmacology/Toxicology</subject><subject>Remission (Medicine)</subject><subject>Review Article</subject><issn>1474-1776</issn><issn>1474-1784</issn><issn>1474-1784</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMo7rr6BzxIwYuXaj6b1JssfsGCB_UckjTRLm2zJi2y_964XVfw4GkG5pl3hgeAUwQvESTiKlLEOMkhpjmEJStzsQemiHKaIy7o_q7nxQQcxbiEEBWI40MwIUKQskR4CsSz_Rhs19eqyeq2HTrfv9ugVuvrrPefKlQxM0OwMXM-ZGro_Qaq-_UxOHCqifZkW2fg9e72Zf6QL57uH-c3i9xgVvS55RwSw1BlXKFoIUypXCUsrUipNUHOFQZzQqF2RFsCNaq4UpY5LSwRGkMyAxdj7ir49GnsZVtHY5tGddYPURJYMMwxZSyh53_QpR9Cl75LFGcMMiJ4ovBImeBjDNbJVahbFdYSQfntVY5eZfIqN16lSEtn2-hBt7barfyITAAZgZhG3ZsNv7f_if0Cq-yDoQ</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Ramírez-Valle, Francisco</creator><creator>Maranville, Joseph C.</creator><creator>Roy, Sophie</creator><creator>Plenge, Robert M.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1688-1573</orcidid><orcidid>https://orcid.org/0000-0002-8625-5869</orcidid></search><sort><creationdate>20240701</creationdate><title>Sequential immunotherapy: towards cures for autoimmunity</title><author>Ramírez-Valle, Francisco ; Maranville, Joseph C. ; Roy, Sophie ; Plenge, Robert M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-e7703c51dcf6a468c9afd8e4d39bb31ff6c27340bf3be30b1d7aae5fb8e38b203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>631/154</topic><topic>631/250/38</topic><topic>Antigens</topic><topic>Autoimmune diseases</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Cancer Research</topic><topic>Homeostasis</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>Medicinal Chemistry</topic><topic>Molecular Medicine</topic><topic>Pharmacology/Toxicology</topic><topic>Remission (Medicine)</topic><topic>Review Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramírez-Valle, Francisco</creatorcontrib><creatorcontrib>Maranville, Joseph C.</creatorcontrib><creatorcontrib>Roy, Sophie</creatorcontrib><creatorcontrib>Plenge, Robert M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Drug discovery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramírez-Valle, Francisco</au><au>Maranville, Joseph C.</au><au>Roy, Sophie</au><au>Plenge, Robert M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequential immunotherapy: towards cures for autoimmunity</atitle><jtitle>Nature reviews. Drug discovery</jtitle><stitle>Nat Rev Drug Discov</stitle><addtitle>Nat Rev Drug Discov</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>23</volume><issue>7</issue><spage>501</spage><epage>524</epage><pages>501-524</pages><issn>1474-1776</issn><issn>1474-1784</issn><eissn>1474-1784</eissn><abstract>Despite major progress in the treatment of autoimmune diseases in the past two decades, most therapies do not cure disease and can be associated with increased risk of infection through broad suppression of the immune system. However, advances in understanding the causes of autoimmune disease and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cell therapies provide evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. Here, we propose a ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal. This framework encompasses three steps: controlling inflammation; resetting the immune system through elimination of pathogenic immune memory cells; and promoting and maintaining immune homeostasis via immune regulatory agents and tissue repair. We discuss existing drugs and those in development for each of the three steps. We also highlight the importance of causal human biology in identifying and prioritizing novel immunotherapeutic strategies as well as informing their application in specific patient subsets, enabling precision medicine approaches that have the potential to transform clinical care. Advances in understanding of the cause of autoimmune diseases and clinical data from novel therapeutic modalities such as chimeric antigen receptor T cells are providing evidence that it may be possible to re-establish immune homeostasis and, potentially, prolong remission or even cure autoimmune diseases. This article proposes a three-step ‘sequential immunotherapy’ framework for immune system modulation to help achieve this ambitious goal, and discusses existing drugs and those in development for each of the three steps.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38839912</pmid><doi>10.1038/s41573-024-00959-8</doi><tpages>24</tpages><orcidid>https://orcid.org/0000-0002-1688-1573</orcidid><orcidid>https://orcid.org/0000-0002-8625-5869</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1474-1776
ispartof Nature reviews. Drug discovery, 2024-07, Vol.23 (7), p.501-524
issn 1474-1776
1474-1784
1474-1784
language eng
recordid cdi_proquest_miscellaneous_3065272455
source Nature Journals Online; SpringerLink Journals - AutoHoldings
subjects 631/154
631/250/38
Antigens
Autoimmune diseases
Biomedical and Life Sciences
Biomedicine
Biotechnology
Cancer Research
Homeostasis
Immune system
Immunotherapy
Medicinal Chemistry
Molecular Medicine
Pharmacology/Toxicology
Remission (Medicine)
Review Article
title Sequential immunotherapy: towards cures for autoimmunity
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T17%3A35%3A56IST&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=Sequential%20immunotherapy:%20towards%20cures%20for%20autoimmunity&rft.jtitle=Nature%20reviews.%20Drug%20discovery&rft.au=Ram%C3%ADrez-Valle,%20Francisco&rft.date=2024-07-01&rft.volume=23&rft.issue=7&rft.spage=501&rft.epage=524&rft.pages=501-524&rft.issn=1474-1776&rft.eissn=1474-1784&rft_id=info:doi/10.1038/s41573-024-00959-8&rft_dat=%3Cproquest_cross%3E3065272455%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=3075505387&rft_id=info:pmid/38839912&rfr_iscdi=true