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Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro

Stimulation of human primary T cells with immobilized anti-CD3 and anti-CD28 Abs in vitro provide a system to study T cell activation and proliferation and an avenue for expanding T cells for immunotherapy. Magnetic beads conjugated with anti-CD3 and anti-CD28 Abs (Dynabeads Human T-Activator [D-TCA...

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Autores principales: Lustig, Ana, Manor, Ty’Keemi, Shi, Guixin, Li, Jiangyuan, Wang, Ying-Ting, An, Yang, Liu, Yu-Tsueng, Weng, Nan-ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433792/
https://www.ncbi.nlm.nih.gov/pubmed/32769179
http://dx.doi.org/10.4049/immunohorizons.2000056
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author Lustig, Ana
Manor, Ty’Keemi
Shi, Guixin
Li, Jiangyuan
Wang, Ying-Ting
An, Yang
Liu, Yu-Tsueng
Weng, Nan-ping
author_facet Lustig, Ana
Manor, Ty’Keemi
Shi, Guixin
Li, Jiangyuan
Wang, Ying-Ting
An, Yang
Liu, Yu-Tsueng
Weng, Nan-ping
author_sort Lustig, Ana
collection PubMed
description Stimulation of human primary T cells with immobilized anti-CD3 and anti-CD28 Abs in vitro provide a system to study T cell activation and proliferation and an avenue for expanding T cells for immunotherapy. Magnetic beads conjugated with anti-CD3 and anti-CD28 Abs (Dynabeads Human T-Activator [D-TCA]) have been a golden standard for stimulating human primary T cells in vitro. In this study, we report that an application using anti-CD3 and anti-CD28 Abs conjugated on lipid microbubbles (microbubble-based human T cell activator [MB-TCA]) to stimulate primary human naive T cells resulted in expansion superior to D-TCA. In 56-d cultures with three repeated stimulation cycles (14 d per stimulation), we found that 1) MB-TCA induced significantly better expansion (20- and 10-fold increase) of naive CD4(+) and CD8(+) T cells than did D-TCA; 2) MB-TCA–and D-TCA–stimulated T cells had a similar number of initial cell divisions, but MB-TCA had significantly lower activation-induced cell death than D-TCA; 3) MB-TCA–stimulated T cells produced less TNF-a than did D-TCA; and 4) blocking TNF-a action via adding an Ab against TNF-αR (TNFRSF1A) significantly improved expansion of T cells activated by D-TCA in vitro. Together, we demonstrated that the MB-TCA induces a better expansion of human naive T cells in vitro and offers advantages in both basic and clinical applications in which the outcome depends on the number of T cells. ImmunoHorizons, 2020, 4: 475–484.
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spelling pubmed-104337922023-08-17 Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro Lustig, Ana Manor, Ty’Keemi Shi, Guixin Li, Jiangyuan Wang, Ying-Ting An, Yang Liu, Yu-Tsueng Weng, Nan-ping Immunohorizons Article Stimulation of human primary T cells with immobilized anti-CD3 and anti-CD28 Abs in vitro provide a system to study T cell activation and proliferation and an avenue for expanding T cells for immunotherapy. Magnetic beads conjugated with anti-CD3 and anti-CD28 Abs (Dynabeads Human T-Activator [D-TCA]) have been a golden standard for stimulating human primary T cells in vitro. In this study, we report that an application using anti-CD3 and anti-CD28 Abs conjugated on lipid microbubbles (microbubble-based human T cell activator [MB-TCA]) to stimulate primary human naive T cells resulted in expansion superior to D-TCA. In 56-d cultures with three repeated stimulation cycles (14 d per stimulation), we found that 1) MB-TCA induced significantly better expansion (20- and 10-fold increase) of naive CD4(+) and CD8(+) T cells than did D-TCA; 2) MB-TCA–and D-TCA–stimulated T cells had a similar number of initial cell divisions, but MB-TCA had significantly lower activation-induced cell death than D-TCA; 3) MB-TCA–stimulated T cells produced less TNF-a than did D-TCA; and 4) blocking TNF-a action via adding an Ab against TNF-αR (TNFRSF1A) significantly improved expansion of T cells activated by D-TCA in vitro. Together, we demonstrated that the MB-TCA induces a better expansion of human naive T cells in vitro and offers advantages in both basic and clinical applications in which the outcome depends on the number of T cells. ImmunoHorizons, 2020, 4: 475–484. 2020-08-07 /pmc/articles/PMC10433792/ /pubmed/32769179 http://dx.doi.org/10.4049/immunohorizons.2000056 Text en https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the CC BY 4.0 Unported license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lustig, Ana
Manor, Ty’Keemi
Shi, Guixin
Li, Jiangyuan
Wang, Ying-Ting
An, Yang
Liu, Yu-Tsueng
Weng, Nan-ping
Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title_full Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title_fullStr Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title_full_unstemmed Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title_short Lipid Microbubble–Conjugated Anti-CD3 and Anti-CD28 Antibodies (Microbubble-Based Human T Cell Activator) Offer Superior Long-Term Expansion of Human Naive T Cells In Vitro
title_sort lipid microbubble–conjugated anti-cd3 and anti-cd28 antibodies (microbubble-based human t cell activator) offer superior long-term expansion of human naive t cells in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433792/
https://www.ncbi.nlm.nih.gov/pubmed/32769179
http://dx.doi.org/10.4049/immunohorizons.2000056
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