Emerging Cellular Therapies: T Cells and Beyond
Cellular therapies, including those based on T cells, are becoming approved options for clinicians treating a range of diseases. Cytotoxic T lymphocytes (CTLs) can be modified ex vivo to express receptors such as chimeric antigen receptors (CARs) or T cell receptors, allowing them to target tumour c...
| 出版年: | Cells |
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| 主要な著者: | , , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
MDPI AG
2019-03-01
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| 主題: | |
| オンライン・アクセス: | https://www.mdpi.com/2073-4409/8/3/284 |
| _version_ | 1850311484580560896 |
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| author | Stephen Todryk Agnieszka Jozwik Julian de Havilland Joanna Hester |
| author_facet | Stephen Todryk Agnieszka Jozwik Julian de Havilland Joanna Hester |
| author_sort | Stephen Todryk |
| collection | DOAJ |
| container_title | Cells |
| description | Cellular therapies, including those based on T cells, are becoming approved options for clinicians treating a range of diseases. Cytotoxic T lymphocytes (CTLs) can be modified ex vivo to express receptors such as chimeric antigen receptors (CARs) or T cell receptors, allowing them to target tumour cells when infused back into patients with particular cancers. CTLs specific for viruses can be purified ex vivo and reinfused into patients transplanted with haematopoietic stem cells to help combat viral reactivation. Regulatory T cells (Tregs) can be expanded ex vivo for infusion into patients with autoimmunity or allergy, or into those at risk of rejecting transplanted cells or tissues, or suffering graft versus host disease. Effector and regulatory T cells can also be generated by infusion of patient-derived dendritic cells (DCs) conditioned in ways to elicit anti-tumour immunity (CTLs) or Tregs. All such therapies are resource-heavy (particularly in process regulation) and so must be initially targeted to patients that have limited treatment options, but also where they have a chance of being effective. |
| format | Article |
| id | doaj-art-24439b2f1e9f4eacb23e96bdc4954625 |
| institution | Directory of Open Access Journals |
| issn | 2073-4409 |
| language | English |
| publishDate | 2019-03-01 |
| publisher | MDPI AG |
| record_format | Article |
| spelling | doaj-art-24439b2f1e9f4eacb23e96bdc49546252025-08-19T23:26:55ZengMDPI AGCells2073-44092019-03-018328410.3390/cells8030284cells8030284Emerging Cellular Therapies: T Cells and BeyondStephen Todryk0Agnieszka Jozwik1Julian de Havilland2Joanna Hester3Department of Applied Sciences, Faculty of Health & Life Sciences, Northumbria University, Newcastle upon Tyne NE1 8ST, UKDepartment of Haematological Medicine, King’s College London, London SE5 9NU, UKNewcastle Biomedicine Cellular Therapies Facility, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 3BZ, UKTransplantation Research and Immunology Group, Nuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 9DU, UKCellular therapies, including those based on T cells, are becoming approved options for clinicians treating a range of diseases. Cytotoxic T lymphocytes (CTLs) can be modified ex vivo to express receptors such as chimeric antigen receptors (CARs) or T cell receptors, allowing them to target tumour cells when infused back into patients with particular cancers. CTLs specific for viruses can be purified ex vivo and reinfused into patients transplanted with haematopoietic stem cells to help combat viral reactivation. Regulatory T cells (Tregs) can be expanded ex vivo for infusion into patients with autoimmunity or allergy, or into those at risk of rejecting transplanted cells or tissues, or suffering graft versus host disease. Effector and regulatory T cells can also be generated by infusion of patient-derived dendritic cells (DCs) conditioned in ways to elicit anti-tumour immunity (CTLs) or Tregs. All such therapies are resource-heavy (particularly in process regulation) and so must be initially targeted to patients that have limited treatment options, but also where they have a chance of being effective.https://www.mdpi.com/2073-4409/8/3/284T cellsregulatory T cellscytotoxic T lymphocytesCARsadoptive therapy |
| spellingShingle | Stephen Todryk Agnieszka Jozwik Julian de Havilland Joanna Hester Emerging Cellular Therapies: T Cells and Beyond T cells regulatory T cells cytotoxic T lymphocytes CARs adoptive therapy |
| title | Emerging Cellular Therapies: T Cells and Beyond |
| title_full | Emerging Cellular Therapies: T Cells and Beyond |
| title_fullStr | Emerging Cellular Therapies: T Cells and Beyond |
| title_full_unstemmed | Emerging Cellular Therapies: T Cells and Beyond |
| title_short | Emerging Cellular Therapies: T Cells and Beyond |
| title_sort | emerging cellular therapies t cells and beyond |
| topic | T cells regulatory T cells cytotoxic T lymphocytes CARs adoptive therapy |
| url | https://www.mdpi.com/2073-4409/8/3/284 |
| work_keys_str_mv | AT stephentodryk emergingcellulartherapiestcellsandbeyond AT agnieszkajozwik emergingcellulartherapiestcellsandbeyond AT juliandehavilland emergingcellulartherapiestcellsandbeyond AT joannahester emergingcellulartherapiestcellsandbeyond |
