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Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells

Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a check point protein expressed on the surface of T cells and plays a central role in regulating the immune response. In recent years, CTLA-4 has become a popular target for cancer immunotherapy in which blocking CTLA-4 can restore T-cell funct...

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Autores principales: Wei, Dong, Horton, Kristin L., Chen, John, Dong, Linlin, Chen, Susan, Abdul-Hadi, Kojo, Zhang, Ting Ting, Casson, Cierra N., Shaw, Michael, Shiraishi, Tsubasa, Wilkinson, Brandon, Ji, Chengjie, Qian, Mark G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142971/
https://www.ncbi.nlm.nih.gov/pubmed/37110545
http://dx.doi.org/10.3390/molecules28083311
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author Wei, Dong
Horton, Kristin L.
Chen, John
Dong, Linlin
Chen, Susan
Abdul-Hadi, Kojo
Zhang, Ting Ting
Casson, Cierra N.
Shaw, Michael
Shiraishi, Tsubasa
Wilkinson, Brandon
Ji, Chengjie
Qian, Mark G.
author_facet Wei, Dong
Horton, Kristin L.
Chen, John
Dong, Linlin
Chen, Susan
Abdul-Hadi, Kojo
Zhang, Ting Ting
Casson, Cierra N.
Shaw, Michael
Shiraishi, Tsubasa
Wilkinson, Brandon
Ji, Chengjie
Qian, Mark G.
author_sort Wei, Dong
collection PubMed
description Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a check point protein expressed on the surface of T cells and plays a central role in regulating the immune response. In recent years, CTLA-4 has become a popular target for cancer immunotherapy in which blocking CTLA-4 can restore T-cell function and enhance the immune response against cancer. Currently, there are many CTLA-4 inhibitors in a variety of modalities, including cell therapies, which are being developed in both preclinical and clinical stages to further harness the potential of the target for the treatment of certain types of cancer. In drug discovery research, measuring the level of CTLA-4 in T cells is important for drug discovery and development because it provides key information for quantitative assessment of the pharmacodynamics, efficacy, and safety of the CTLA-4-based therapies. However, to our best knowledge, there is still no report of a sensitive, specific, accurate, and reliable assay for CTLA-4 measurement. In this work, an LC/MS-based method was developed to measure CTLA-4 in human T cells. The assay demonstrated high specificity with an LLOQ of 5 copies of CTLA-4 per cell when using 2.5 million T cells for analysis. As shown in the work, the assay was successfully used to measure CTLA-4 levels in subtype T-cell samples from individual healthy subjects. The assay could be applied in supporting the studies of CTLA-4-based cancer therapies.
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spelling pubmed-101429712023-04-29 Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells Wei, Dong Horton, Kristin L. Chen, John Dong, Linlin Chen, Susan Abdul-Hadi, Kojo Zhang, Ting Ting Casson, Cierra N. Shaw, Michael Shiraishi, Tsubasa Wilkinson, Brandon Ji, Chengjie Qian, Mark G. Molecules Article Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a check point protein expressed on the surface of T cells and plays a central role in regulating the immune response. In recent years, CTLA-4 has become a popular target for cancer immunotherapy in which blocking CTLA-4 can restore T-cell function and enhance the immune response against cancer. Currently, there are many CTLA-4 inhibitors in a variety of modalities, including cell therapies, which are being developed in both preclinical and clinical stages to further harness the potential of the target for the treatment of certain types of cancer. In drug discovery research, measuring the level of CTLA-4 in T cells is important for drug discovery and development because it provides key information for quantitative assessment of the pharmacodynamics, efficacy, and safety of the CTLA-4-based therapies. However, to our best knowledge, there is still no report of a sensitive, specific, accurate, and reliable assay for CTLA-4 measurement. In this work, an LC/MS-based method was developed to measure CTLA-4 in human T cells. The assay demonstrated high specificity with an LLOQ of 5 copies of CTLA-4 per cell when using 2.5 million T cells for analysis. As shown in the work, the assay was successfully used to measure CTLA-4 levels in subtype T-cell samples from individual healthy subjects. The assay could be applied in supporting the studies of CTLA-4-based cancer therapies. MDPI 2023-04-08 /pmc/articles/PMC10142971/ /pubmed/37110545 http://dx.doi.org/10.3390/molecules28083311 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Wei, Dong
Horton, Kristin L.
Chen, John
Dong, Linlin
Chen, Susan
Abdul-Hadi, Kojo
Zhang, Ting Ting
Casson, Cierra N.
Shaw, Michael
Shiraishi, Tsubasa
Wilkinson, Brandon
Ji, Chengjie
Qian, Mark G.
Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title_full Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title_fullStr Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title_full_unstemmed Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title_short Development of a Highly Sensitive Hybrid LC/MS Assay for the Quantitative Measurement of CTLA-4 in Human T Cells
title_sort development of a highly sensitive hybrid lc/ms assay for the quantitative measurement of ctla-4 in human t cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142971/
https://www.ncbi.nlm.nih.gov/pubmed/37110545
http://dx.doi.org/10.3390/molecules28083311
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