Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy

Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancers 2023-07, Vol.15 (13), p.3476
Hauptverfasser: Zheng, Zhibo, Li, Siyuan, Liu, Mohan, Chen, Chuyan, Zhang, Lu, Zhou, Daobin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 13
container_start_page 3476
container_title Cancers
container_volume 15
creator Zheng, Zhibo
Li, Siyuan
Liu, Mohan
Chen, Chuyan
Zhang, Lu
Zhou, Daobin
description Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of cancer. However, the initial success of first-generation CAR-T cells was limited due to inadequate proliferation and undesirable outcomes. Nonetheless, significant progress has been made in CAR-T cell engineering, leading to the development of the latest fifth-generation CAR-T cells that can target multiple antigens and overcome individual limitations. Despite these advancements, some shortcomings prevent the widespread use of CAR-T therapy, including life-threatening toxicities, T-cell exhaustion, and inadequate infiltration for solid tumors. Researchers have made considerable efforts to address these issues by developing new strategies for improving CAR-T cell function and reducing toxicities. This review provides an overview of the path of CAR-T cell development and highlights some of the prominent advances in its structure and manufacturing process, which include the strategies to improve antigen recognition, enhance T-cell activation and persistence, and overcome immune escape. Finally, the review briefly covers other immune cells for cancer therapy and ends with the discussion on the broad prospects of CAR-T in the treatment of various diseases, not just hematological tumors, and the challenges that need to be addressed for the widespread clinical application of CAR-T cell therapies.
doi_str_mv 10.3390/cancers15133476
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10340266</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A757714556</galeid><sourcerecordid>A757714556</sourcerecordid><originalsourceid>FETCH-LOGICAL-c489t-e976d3258d4c1dae7218166097d5b1f6d5a301d8616175e903db15ed158de31b3</originalsourceid><addsrcrecordid>eNptkk1v1DAQhiMEolXpmRuyxIVLWk_8lXBBq1VbKlUCwcLV8tqTXVdZe7GTSv33OOoHbYV98Nh-3nc09lTVe6AnjHX01JpgMWUQwBhX8lV12FDV1FJ2_PWT-KA6zvmalsEYKKneVgdMcc5FKw-r3-c-YL2agg8bMm5TnDZbcoEBkxl9DPkzWbibOU8mPpCfY5rsOCUkJjjyPUVXtgUjsSfLxY96RVbbotzfvqve9GbIeHy_HlW_zs9Wy6_11beLy-Xiqra87cYaOyUda0TruAVnUDXQgpS0U06soZdOGEbBtRIkKIEdZW4NAh0UBTJYs6Pqy53vflrv0FkMYzKD3ie_M-lWR-P185vgt3oTbzRQxmkjZXH4dO-Q4p8J86h3PlscBhMwTlk3LWsbzhnwgn58gV7HKYVS30zJ2VC0_6iNGVD70MeS2M6meqGEUsCFmNOe_Icq0-HO2xiw9-X8meD0TmBTzDlh_1gkUD23g37RDkXx4enbPPIPn8_-Arfhr2g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2836340258</pqid></control><display><type>article</type><title>Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy</title><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Zheng, Zhibo ; Li, Siyuan ; Liu, Mohan ; Chen, Chuyan ; Zhang, Lu ; Zhou, Daobin</creator><creatorcontrib>Zheng, Zhibo ; Li, Siyuan ; Liu, Mohan ; Chen, Chuyan ; Zhang, Lu ; Zhou, Daobin</creatorcontrib><description>Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of cancer. However, the initial success of first-generation CAR-T cells was limited due to inadequate proliferation and undesirable outcomes. Nonetheless, significant progress has been made in CAR-T cell engineering, leading to the development of the latest fifth-generation CAR-T cells that can target multiple antigens and overcome individual limitations. Despite these advancements, some shortcomings prevent the widespread use of CAR-T therapy, including life-threatening toxicities, T-cell exhaustion, and inadequate infiltration for solid tumors. Researchers have made considerable efforts to address these issues by developing new strategies for improving CAR-T cell function and reducing toxicities. This review provides an overview of the path of CAR-T cell development and highlights some of the prominent advances in its structure and manufacturing process, which include the strategies to improve antigen recognition, enhance T-cell activation and persistence, and overcome immune escape. Finally, the review briefly covers other immune cells for cancer therapy and ends with the discussion on the broad prospects of CAR-T in the treatment of various diseases, not just hematological tumors, and the challenges that need to be addressed for the widespread clinical application of CAR-T cell therapies.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15133476</identifier><identifier>PMID: 37444586</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antigens ; Autoimmune diseases ; B cells ; Cancer ; Cancer therapies ; Care and treatment ; CD19 antigen ; Cell activation ; Cell proliferation ; Cell therapy ; Chimeric antigen receptors ; Clinical trials ; Cytokines ; Design ; Drug approval ; Drug therapy ; Fibrosis ; Genetically modified organisms ; Graft-versus-host reaction ; Health aspects ; Hematology ; Immunotherapy ; Leukemia ; Lymphocytes ; Lymphocytes T ; Lymphoma ; Malignancy ; Melanoma ; Metastases ; Non-Hodgkin's lymphomas ; Patients ; Review ; Reviews ; Solid tumors ; T cells ; Tumors ; Virus diseases</subject><ispartof>Cancers, 2023-07, Vol.15 (13), p.3476</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-e976d3258d4c1dae7218166097d5b1f6d5a301d8616175e903db15ed158de31b3</citedby><cites>FETCH-LOGICAL-c489t-e976d3258d4c1dae7218166097d5b1f6d5a301d8616175e903db15ed158de31b3</cites><orcidid>0000-0003-1654-3571</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340266/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340266/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37444586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Zhibo</creatorcontrib><creatorcontrib>Li, Siyuan</creatorcontrib><creatorcontrib>Liu, Mohan</creatorcontrib><creatorcontrib>Chen, Chuyan</creatorcontrib><creatorcontrib>Zhang, Lu</creatorcontrib><creatorcontrib>Zhou, Daobin</creatorcontrib><title>Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of cancer. However, the initial success of first-generation CAR-T cells was limited due to inadequate proliferation and undesirable outcomes. Nonetheless, significant progress has been made in CAR-T cell engineering, leading to the development of the latest fifth-generation CAR-T cells that can target multiple antigens and overcome individual limitations. Despite these advancements, some shortcomings prevent the widespread use of CAR-T therapy, including life-threatening toxicities, T-cell exhaustion, and inadequate infiltration for solid tumors. Researchers have made considerable efforts to address these issues by developing new strategies for improving CAR-T cell function and reducing toxicities. This review provides an overview of the path of CAR-T cell development and highlights some of the prominent advances in its structure and manufacturing process, which include the strategies to improve antigen recognition, enhance T-cell activation and persistence, and overcome immune escape. Finally, the review briefly covers other immune cells for cancer therapy and ends with the discussion on the broad prospects of CAR-T in the treatment of various diseases, not just hematological tumors, and the challenges that need to be addressed for the widespread clinical application of CAR-T cell therapies.</description><subject>Antigens</subject><subject>Autoimmune diseases</subject><subject>B cells</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>CD19 antigen</subject><subject>Cell activation</subject><subject>Cell proliferation</subject><subject>Cell therapy</subject><subject>Chimeric antigen receptors</subject><subject>Clinical trials</subject><subject>Cytokines</subject><subject>Design</subject><subject>Drug approval</subject><subject>Drug therapy</subject><subject>Fibrosis</subject><subject>Genetically modified organisms</subject><subject>Graft-versus-host reaction</subject><subject>Health aspects</subject><subject>Hematology</subject><subject>Immunotherapy</subject><subject>Leukemia</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Lymphoma</subject><subject>Malignancy</subject><subject>Melanoma</subject><subject>Metastases</subject><subject>Non-Hodgkin's lymphomas</subject><subject>Patients</subject><subject>Review</subject><subject>Reviews</subject><subject>Solid tumors</subject><subject>T cells</subject><subject>Tumors</subject><subject>Virus diseases</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1v1DAQhiMEolXpmRuyxIVLWk_8lXBBq1VbKlUCwcLV8tqTXVdZe7GTSv33OOoHbYV98Nh-3nc09lTVe6AnjHX01JpgMWUQwBhX8lV12FDV1FJ2_PWT-KA6zvmalsEYKKneVgdMcc5FKw-r3-c-YL2agg8bMm5TnDZbcoEBkxl9DPkzWbibOU8mPpCfY5rsOCUkJjjyPUVXtgUjsSfLxY96RVbbotzfvqve9GbIeHy_HlW_zs9Wy6_11beLy-Xiqra87cYaOyUda0TruAVnUDXQgpS0U06soZdOGEbBtRIkKIEdZW4NAh0UBTJYs6Pqy53vflrv0FkMYzKD3ie_M-lWR-P185vgt3oTbzRQxmkjZXH4dO-Q4p8J86h3PlscBhMwTlk3LWsbzhnwgn58gV7HKYVS30zJ2VC0_6iNGVD70MeS2M6meqGEUsCFmNOe_Icq0-HO2xiw9-X8meD0TmBTzDlh_1gkUD23g37RDkXx4enbPPIPn8_-Arfhr2g</recordid><startdate>20230703</startdate><enddate>20230703</enddate><creator>Zheng, Zhibo</creator><creator>Li, Siyuan</creator><creator>Liu, Mohan</creator><creator>Chen, Chuyan</creator><creator>Zhang, Lu</creator><creator>Zhou, Daobin</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1654-3571</orcidid></search><sort><creationdate>20230703</creationdate><title>Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy</title><author>Zheng, Zhibo ; Li, Siyuan ; Liu, Mohan ; Chen, Chuyan ; Zhang, Lu ; Zhou, Daobin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-e976d3258d4c1dae7218166097d5b1f6d5a301d8616175e903db15ed158de31b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigens</topic><topic>Autoimmune diseases</topic><topic>B cells</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>CD19 antigen</topic><topic>Cell activation</topic><topic>Cell proliferation</topic><topic>Cell therapy</topic><topic>Chimeric antigen receptors</topic><topic>Clinical trials</topic><topic>Cytokines</topic><topic>Design</topic><topic>Drug approval</topic><topic>Drug therapy</topic><topic>Fibrosis</topic><topic>Genetically modified organisms</topic><topic>Graft-versus-host reaction</topic><topic>Health aspects</topic><topic>Hematology</topic><topic>Immunotherapy</topic><topic>Leukemia</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Lymphoma</topic><topic>Malignancy</topic><topic>Melanoma</topic><topic>Metastases</topic><topic>Non-Hodgkin's lymphomas</topic><topic>Patients</topic><topic>Review</topic><topic>Reviews</topic><topic>Solid tumors</topic><topic>T cells</topic><topic>Tumors</topic><topic>Virus diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Zhibo</creatorcontrib><creatorcontrib>Li, Siyuan</creatorcontrib><creatorcontrib>Liu, Mohan</creatorcontrib><creatorcontrib>Chen, Chuyan</creatorcontrib><creatorcontrib>Zhang, Lu</creatorcontrib><creatorcontrib>Zhou, Daobin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Zhibo</au><au>Li, Siyuan</au><au>Liu, Mohan</au><au>Chen, Chuyan</au><au>Zhang, Lu</au><au>Zhou, Daobin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-07-03</date><risdate>2023</risdate><volume>15</volume><issue>13</issue><spage>3476</spage><pages>3476-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Chimeric antigen receptor (CAR)-T cell therapy is a promising form of immunotherapy that has seen significant advancements in the past few decades. It involves genetically modifying T cells to target cancer cells expressing specific antigens, providing a novel approach to treating various types of cancer. However, the initial success of first-generation CAR-T cells was limited due to inadequate proliferation and undesirable outcomes. Nonetheless, significant progress has been made in CAR-T cell engineering, leading to the development of the latest fifth-generation CAR-T cells that can target multiple antigens and overcome individual limitations. Despite these advancements, some shortcomings prevent the widespread use of CAR-T therapy, including life-threatening toxicities, T-cell exhaustion, and inadequate infiltration for solid tumors. Researchers have made considerable efforts to address these issues by developing new strategies for improving CAR-T cell function and reducing toxicities. This review provides an overview of the path of CAR-T cell development and highlights some of the prominent advances in its structure and manufacturing process, which include the strategies to improve antigen recognition, enhance T-cell activation and persistence, and overcome immune escape. Finally, the review briefly covers other immune cells for cancer therapy and ends with the discussion on the broad prospects of CAR-T in the treatment of various diseases, not just hematological tumors, and the challenges that need to be addressed for the widespread clinical application of CAR-T cell therapies.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37444586</pmid><doi>10.3390/cancers15133476</doi><orcidid>https://orcid.org/0000-0003-1654-3571</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2072-6694
ispartof Cancers, 2023-07, Vol.15 (13), p.3476
issn 2072-6694
2072-6694
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10340266
source PubMed Central Open Access; MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Antigens
Autoimmune diseases
B cells
Cancer
Cancer therapies
Care and treatment
CD19 antigen
Cell activation
Cell proliferation
Cell therapy
Chimeric antigen receptors
Clinical trials
Cytokines
Design
Drug approval
Drug therapy
Fibrosis
Genetically modified organisms
Graft-versus-host reaction
Health aspects
Hematology
Immunotherapy
Leukemia
Lymphocytes
Lymphocytes T
Lymphoma
Malignancy
Melanoma
Metastases
Non-Hodgkin's lymphomas
Patients
Review
Reviews
Solid tumors
T cells
Tumors
Virus diseases
title Fine-Tuning through Generations: Advances in Structure and Production of CAR-T Therapy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T18%3A09%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fine-Tuning%20through%20Generations:%20Advances%20in%20Structure%20and%20Production%20of%20CAR-T%20Therapy&rft.jtitle=Cancers&rft.au=Zheng,%20Zhibo&rft.date=2023-07-03&rft.volume=15&rft.issue=13&rft.spage=3476&rft.pages=3476-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers15133476&rft_dat=%3Cgale_pubme%3EA757714556%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2836340258&rft_id=info:pmid/37444586&rft_galeid=A757714556&rfr_iscdi=true