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Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer
Chimeric antigen receptor (CAR) T cells represent a novel targeted approach to overcome both quantitative and qualitative shortfalls of the host immune system relating to the detection and subsequent destruction of tumors. The identification of antigens expressed specifically on the surface of tumor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895166/ https://www.ncbi.nlm.nih.gov/pubmed/29239915 http://dx.doi.org/10.1097/CJI.0000000000000203 |
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author | Owens, Gemma L. Sheard, Victoria E. Kalaitsidou, Milena Blount, Daniel Lad, Yatish Cheadle, Eleanor J. Edmondson, Richard J. Kooner, Gurdeep Gilham, David E. Harrop, Richard |
author_facet | Owens, Gemma L. Sheard, Victoria E. Kalaitsidou, Milena Blount, Daniel Lad, Yatish Cheadle, Eleanor J. Edmondson, Richard J. Kooner, Gurdeep Gilham, David E. Harrop, Richard |
author_sort | Owens, Gemma L. |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cells represent a novel targeted approach to overcome both quantitative and qualitative shortfalls of the host immune system relating to the detection and subsequent destruction of tumors. The identification of antigens expressed specifically on the surface of tumor cells is a critical first step in the ability to utilize CAR T cells for the treatment of cancer. The 5T4 is a tumor-associated antigen which is expressed on the cell surface of most solid tumors including ovarian cancer. Matched blood and tumor samples were collected from 12 patients with ovarian cancer; all tumors were positive for 5T4 expression by immunohistochemistry. Patient T cells were effectively transduced with 2 different anti-5T4 CAR constructs which differed in their affinity for the target antigen. Co-culture of CAR T cells with matched autologous tumor disaggregates resulted in antigen-specific secretion of IFN-gamma. Furthermore, assessment of the efficacy of anti-5T4 CAR T cells in a mouse model resulted in therapeutic benefit against established ovarian tumors. These results demonstrate proof of principle that 5T4 is an attractive target for immune intervention in ovarian cancer and that patient T cells engineered to express a 5T4-specific CAR can recognize and respond physiologically to autologous tumor cells. |
format | Online Article Text |
id | pubmed-5895166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-58951662018-04-27 Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer Owens, Gemma L. Sheard, Victoria E. Kalaitsidou, Milena Blount, Daniel Lad, Yatish Cheadle, Eleanor J. Edmondson, Richard J. Kooner, Gurdeep Gilham, David E. Harrop, Richard J Immunother Basic Studies Chimeric antigen receptor (CAR) T cells represent a novel targeted approach to overcome both quantitative and qualitative shortfalls of the host immune system relating to the detection and subsequent destruction of tumors. The identification of antigens expressed specifically on the surface of tumor cells is a critical first step in the ability to utilize CAR T cells for the treatment of cancer. The 5T4 is a tumor-associated antigen which is expressed on the cell surface of most solid tumors including ovarian cancer. Matched blood and tumor samples were collected from 12 patients with ovarian cancer; all tumors were positive for 5T4 expression by immunohistochemistry. Patient T cells were effectively transduced with 2 different anti-5T4 CAR constructs which differed in their affinity for the target antigen. Co-culture of CAR T cells with matched autologous tumor disaggregates resulted in antigen-specific secretion of IFN-gamma. Furthermore, assessment of the efficacy of anti-5T4 CAR T cells in a mouse model resulted in therapeutic benefit against established ovarian tumors. These results demonstrate proof of principle that 5T4 is an attractive target for immune intervention in ovarian cancer and that patient T cells engineered to express a 5T4-specific CAR can recognize and respond physiologically to autologous tumor cells. Lippincott Williams & Wilkins 2018-04 2018-03-20 /pmc/articles/PMC5895166/ /pubmed/29239915 http://dx.doi.org/10.1097/CJI.0000000000000203 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Basic Studies Owens, Gemma L. Sheard, Victoria E. Kalaitsidou, Milena Blount, Daniel Lad, Yatish Cheadle, Eleanor J. Edmondson, Richard J. Kooner, Gurdeep Gilham, David E. Harrop, Richard Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title | Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title_full | Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title_fullStr | Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title_full_unstemmed | Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title_short | Preclinical Assessment of CAR T-Cell Therapy Targeting the Tumor Antigen 5T4 in Ovarian Cancer |
title_sort | preclinical assessment of car t-cell therapy targeting the tumor antigen 5t4 in ovarian cancer |
topic | Basic Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895166/ https://www.ncbi.nlm.nih.gov/pubmed/29239915 http://dx.doi.org/10.1097/CJI.0000000000000203 |
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