Extracellular vesicles as next generation immunotherapeutics

Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of vario...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Seminars in cancer biology 2023-05, Vol.90, p.73-100
Hauptverfasser: Greening, David W., Xu, Rong, Ale, Anukreity, Hagemeyer, Christoph E., Chen, Weisan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 100
container_issue
container_start_page 73
container_title Seminars in cancer biology
container_volume 90
creator Greening, David W.
Xu, Rong
Ale, Anukreity
Hagemeyer, Christoph E.
Chen, Weisan
description Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.
doi_str_mv 10.1016/j.semcancer.2023.02.002
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2775619880</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1044579X23000172</els_id><sourcerecordid>2775619880</sourcerecordid><originalsourceid>FETCH-LOGICAL-c371t-44b37c33dfd6833f9680fb50a06631920b79869fc2b9db8597c1b0f0f09904963</originalsourceid><addsrcrecordid>eNqFkE1LxDAQhoMorq7-Be3RS-skaZMGvCyyfoDgRcFbSNOpZunHmrSL_nuz7OpV5jAz8L7z8RBySSGjQMX1KgvYWdNb9BkDxjNgGQA7ICcUlEi5KOBwW-d5Wkj1NiOnIawAQOU0PyYzLqTkJYMTcrP8Gr2x2LZTa3yyweBsiyExIenxa0zesUdvRjf0ieu6qR_Gj9ivcRqdDWfkqDFtwPN9npPXu-XL7UP69Hz_eLt4Si2XdEzzvOLScl43tSg5b5QooakKMCAEp4pBJVUpVGNZpeqqLJS0tIImhlKQK8Hn5Go3d-2HzwnDqDsXtjebHocpaCZlIagqS4hSuZNaP4TgsdFr7zrjvzUFvUWnV_oPnd6i08B0RBedF_slU9Vh_ef7ZRUFi50A46sbF-3BOoxzaufRjroe3L9LfgBbqIPA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2775619880</pqid></control><display><type>article</type><title>Extracellular vesicles as next generation immunotherapeutics</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Greening, David W. ; Xu, Rong ; Ale, Anukreity ; Hagemeyer, Christoph E. ; Chen, Weisan</creator><creatorcontrib>Greening, David W. ; Xu, Rong ; Ale, Anukreity ; Hagemeyer, Christoph E. ; Chen, Weisan</creatorcontrib><description>Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.</description><identifier>ISSN: 1044-579X</identifier><identifier>EISSN: 1096-3650</identifier><identifier>DOI: 10.1016/j.semcancer.2023.02.002</identifier><identifier>PMID: 36773820</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Antigen Presentation ; Cancer ; Extracellular vesicles ; Extracellular Vesicles - metabolism ; Humans ; Immunity ; Immunologic Surveillance ; Immunoregulation ; Immunosurveillance ; Immunotherapy ; Microenvironment ; Nanovesicles ; Neoplasms - pathology ; Tumor Microenvironment ; Vaccine</subject><ispartof>Seminars in cancer biology, 2023-05, Vol.90, p.73-100</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-44b37c33dfd6833f9680fb50a06631920b79869fc2b9db8597c1b0f0f09904963</citedby><cites>FETCH-LOGICAL-c371t-44b37c33dfd6833f9680fb50a06631920b79869fc2b9db8597c1b0f0f09904963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1044579X23000172$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36773820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Greening, David W.</creatorcontrib><creatorcontrib>Xu, Rong</creatorcontrib><creatorcontrib>Ale, Anukreity</creatorcontrib><creatorcontrib>Hagemeyer, Christoph E.</creatorcontrib><creatorcontrib>Chen, Weisan</creatorcontrib><title>Extracellular vesicles as next generation immunotherapeutics</title><title>Seminars in cancer biology</title><addtitle>Semin Cancer Biol</addtitle><description>Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.</description><subject>Antigen Presentation</subject><subject>Cancer</subject><subject>Extracellular vesicles</subject><subject>Extracellular Vesicles - metabolism</subject><subject>Humans</subject><subject>Immunity</subject><subject>Immunologic Surveillance</subject><subject>Immunoregulation</subject><subject>Immunosurveillance</subject><subject>Immunotherapy</subject><subject>Microenvironment</subject><subject>Nanovesicles</subject><subject>Neoplasms - pathology</subject><subject>Tumor Microenvironment</subject><subject>Vaccine</subject><issn>1044-579X</issn><issn>1096-3650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAQhoMorq7-Be3RS-skaZMGvCyyfoDgRcFbSNOpZunHmrSL_nuz7OpV5jAz8L7z8RBySSGjQMX1KgvYWdNb9BkDxjNgGQA7ICcUlEi5KOBwW-d5Wkj1NiOnIawAQOU0PyYzLqTkJYMTcrP8Gr2x2LZTa3yyweBsiyExIenxa0zesUdvRjf0ieu6qR_Gj9ivcRqdDWfkqDFtwPN9npPXu-XL7UP69Hz_eLt4Si2XdEzzvOLScl43tSg5b5QooakKMCAEp4pBJVUpVGNZpeqqLJS0tIImhlKQK8Hn5Go3d-2HzwnDqDsXtjebHocpaCZlIagqS4hSuZNaP4TgsdFr7zrjvzUFvUWnV_oPnd6i08B0RBedF_slU9Vh_ef7ZRUFi50A46sbF-3BOoxzaufRjroe3L9LfgBbqIPA</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Greening, David W.</creator><creator>Xu, Rong</creator><creator>Ale, Anukreity</creator><creator>Hagemeyer, Christoph E.</creator><creator>Chen, Weisan</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></search><sort><creationdate>202305</creationdate><title>Extracellular vesicles as next generation immunotherapeutics</title><author>Greening, David W. ; Xu, Rong ; Ale, Anukreity ; Hagemeyer, Christoph E. ; Chen, Weisan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-44b37c33dfd6833f9680fb50a06631920b79869fc2b9db8597c1b0f0f09904963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigen Presentation</topic><topic>Cancer</topic><topic>Extracellular vesicles</topic><topic>Extracellular Vesicles - metabolism</topic><topic>Humans</topic><topic>Immunity</topic><topic>Immunologic Surveillance</topic><topic>Immunoregulation</topic><topic>Immunosurveillance</topic><topic>Immunotherapy</topic><topic>Microenvironment</topic><topic>Nanovesicles</topic><topic>Neoplasms - pathology</topic><topic>Tumor Microenvironment</topic><topic>Vaccine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Greening, David W.</creatorcontrib><creatorcontrib>Xu, Rong</creatorcontrib><creatorcontrib>Ale, Anukreity</creatorcontrib><creatorcontrib>Hagemeyer, Christoph E.</creatorcontrib><creatorcontrib>Chen, Weisan</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><jtitle>Seminars in cancer biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Greening, David W.</au><au>Xu, Rong</au><au>Ale, Anukreity</au><au>Hagemeyer, Christoph E.</au><au>Chen, Weisan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extracellular vesicles as next generation immunotherapeutics</atitle><jtitle>Seminars in cancer biology</jtitle><addtitle>Semin Cancer Biol</addtitle><date>2023-05</date><risdate>2023</risdate><volume>90</volume><spage>73</spage><epage>100</epage><pages>73-100</pages><issn>1044-579X</issn><eissn>1096-3650</eissn><abstract>Extracellular vesicles (EVs) function as a mode of intercellular communication and molecular transfer to elicit diverse biological/functional response. Accumulating evidence has highlighted that EVs from immune, tumour, stromal cells and even bacteria and parasites mediate the communication of various immune cell types to dynamically regulate host immune response. EVs have an innate capacity to evade recognition, transport and transfer functional components to target cells, with subsequent removal by the immune system, where the immunological activities of EVs impact immunoregulation including modulation of antigen presentation and cross-dressing, immune activation, immune suppression, and immune surveillance, impacting the tumour immune microenvironment. In this review, we outline the recent progress of EVs in immunorecognition and therapeutic intervention in cancer, including vaccine and targeted drug delivery and summarise their utility towards clinical translation. We highlight the strategies where EVs (natural and engineered) are being employed as a therapeutic approach for immunogenicity, tumoricidal function, and vaccine development, termed immuno-EVs. With seminal studies providing significant progress in the sequential development of engineered EVs as therapeutic anti-tumour platforms, we now require direct assessment to tune and improve the efficacy of resulting immune responses - essential in their translation into the clinic. We believe such a review could strengthen our understanding of the progress in EV immunobiology and facilitate advances in engineering EVs for the development of novel EV-based immunotherapeutics as a platform for cancer treatment.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36773820</pmid><doi>10.1016/j.semcancer.2023.02.002</doi><tpages>28</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1044-579X
ispartof Seminars in cancer biology, 2023-05, Vol.90, p.73-100
issn 1044-579X
1096-3650
language eng
recordid cdi_proquest_miscellaneous_2775619880
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Antigen Presentation
Cancer
Extracellular vesicles
Extracellular Vesicles - metabolism
Humans
Immunity
Immunologic Surveillance
Immunoregulation
Immunosurveillance
Immunotherapy
Microenvironment
Nanovesicles
Neoplasms - pathology
Tumor Microenvironment
Vaccine
title Extracellular vesicles as next generation immunotherapeutics
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T13%3A32%3A12IST&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=Extracellular%20vesicles%20as%20next%20generation%20immunotherapeutics&rft.jtitle=Seminars%20in%20cancer%20biology&rft.au=Greening,%20David%20W.&rft.date=2023-05&rft.volume=90&rft.spage=73&rft.epage=100&rft.pages=73-100&rft.issn=1044-579X&rft.eissn=1096-3650&rft_id=info:doi/10.1016/j.semcancer.2023.02.002&rft_dat=%3Cproquest_cross%3E2775619880%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=2775619880&rft_id=info:pmid/36773820&rft_els_id=S1044579X23000172&rfr_iscdi=true