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...
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Veröffentlicht in: | Cancers 2023-07, Vol.15 (13), p.3476 |
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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 |
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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/). 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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> |
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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 |
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