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Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction
Invariant natural killer T (iNKT) cells are a non-conventional T-cell population expressing a conserved semi-invariant T-cell receptor (TCR) that reacts to lipid antigens, such as α-galactosyl ceramide (α-GalCer), presented by the monomorphic molecule CD1d. iNKT cells play a central role in tumor im...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Bio-Protocol
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336563/ https://www.ncbi.nlm.nih.gov/pubmed/37449036 http://dx.doi.org/10.21769/BioProtoc.4707 |
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author | Delfanti, Gloria Dellabona, Paolo Casorati, Giulia |
author_facet | Delfanti, Gloria Dellabona, Paolo Casorati, Giulia |
author_sort | Delfanti, Gloria |
collection | PubMed |
description | Invariant natural killer T (iNKT) cells are a non-conventional T-cell population expressing a conserved semi-invariant T-cell receptor (TCR) that reacts to lipid antigens, such as α-galactosyl ceramide (α-GalCer), presented by the monomorphic molecule CD1d. iNKT cells play a central role in tumor immunosurveillance and represent a powerful tool for anti-cancer treatment, notably because they can be efficiently redirected against hematological or solid malignancies by engineering with tumor-specific chimeric antigen receptors (CARs) or TCRs. However, iNKT cells are rare and require specific ex vivo pre-selection and substantial in vitro expansion to be exploited for adoptive cell therapy (ACT). This protocol describes a robust method to obtain a large number of mouse iNKT cells that can be effectually engineered by retroviral (RV) transduction. A major advantage of this protocol is that it requires neither particular instrumentation nor a high number of mice. iNKT cells are enriched from the spleens of iVα14-Jα18 transgenic mice; the rapid purification protocol yields a highly enriched iNKT cell population that is activated by anti-CD3/CD28 beads, which is more reproducible and less time consuming than using bone marrow–derived dendritic cells loaded with α-GalCer, without risks of expanding contaminant T cells. Forty-eight hours after activation, iNKT cells are transduced with the selected RV by spin inoculation. This protocol allows to obtain, in 15 days, millions of ready-to-use, highly pure, and stably transduced iNKT cells that might be exploited for in vitro assays and ACT experiments in preclinical studies. |
format | Online Article Text |
id | pubmed-10336563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bio-Protocol |
record_format | MEDLINE/PubMed |
spelling | pubmed-103365632023-07-13 Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction Delfanti, Gloria Dellabona, Paolo Casorati, Giulia Bio Protoc Methods Article Invariant natural killer T (iNKT) cells are a non-conventional T-cell population expressing a conserved semi-invariant T-cell receptor (TCR) that reacts to lipid antigens, such as α-galactosyl ceramide (α-GalCer), presented by the monomorphic molecule CD1d. iNKT cells play a central role in tumor immunosurveillance and represent a powerful tool for anti-cancer treatment, notably because they can be efficiently redirected against hematological or solid malignancies by engineering with tumor-specific chimeric antigen receptors (CARs) or TCRs. However, iNKT cells are rare and require specific ex vivo pre-selection and substantial in vitro expansion to be exploited for adoptive cell therapy (ACT). This protocol describes a robust method to obtain a large number of mouse iNKT cells that can be effectually engineered by retroviral (RV) transduction. A major advantage of this protocol is that it requires neither particular instrumentation nor a high number of mice. iNKT cells are enriched from the spleens of iVα14-Jα18 transgenic mice; the rapid purification protocol yields a highly enriched iNKT cell population that is activated by anti-CD3/CD28 beads, which is more reproducible and less time consuming than using bone marrow–derived dendritic cells loaded with α-GalCer, without risks of expanding contaminant T cells. Forty-eight hours after activation, iNKT cells are transduced with the selected RV by spin inoculation. This protocol allows to obtain, in 15 days, millions of ready-to-use, highly pure, and stably transduced iNKT cells that might be exploited for in vitro assays and ACT experiments in preclinical studies. Bio-Protocol 2023-07-05 /pmc/articles/PMC10336563/ /pubmed/37449036 http://dx.doi.org/10.21769/BioProtoc.4707 Text en ©Copyright : © 2023 The Authors; This is an open access article under the CC BY-NC license https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/). |
spellingShingle | Methods Article Delfanti, Gloria Dellabona, Paolo Casorati, Giulia Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title | Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title_full | Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title_fullStr | Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title_full_unstemmed | Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title_short | Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction |
title_sort | primary mouse invariant natural killer t (inkt) cell purification and transduction |
topic | Methods Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336563/ https://www.ncbi.nlm.nih.gov/pubmed/37449036 http://dx.doi.org/10.21769/BioProtoc.4707 |
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