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Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia
OBJECTIVES: Natural killer (NK) cells are an attractive source of cells for an ‘off the shelf’ cellular therapy because of their innate capacity to target malignant cells, and ability to be transferred between donors and patients. However, since not all NK cells are equally effective at targeting ca...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365579/ https://www.ncbi.nlm.nih.gov/pubmed/32695339 http://dx.doi.org/10.1002/cti2.1151 |
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author | Foley, Bree Ta, Clara Barnes, Samantha de Jong, Emma Nguyen, Michelle Cheung, Laurence C Buzzai, Anthony Wagner, Teagan Wylie, Ben Fernandez, Sonia Cruickshank, Mark Endersby, Raelene Kees, Ursula Waithman, Jason |
author_facet | Foley, Bree Ta, Clara Barnes, Samantha de Jong, Emma Nguyen, Michelle Cheung, Laurence C Buzzai, Anthony Wagner, Teagan Wylie, Ben Fernandez, Sonia Cruickshank, Mark Endersby, Raelene Kees, Ursula Waithman, Jason |
author_sort | Foley, Bree |
collection | PubMed |
description | OBJECTIVES: Natural killer (NK) cells are an attractive source of cells for an ‘off the shelf’ cellular therapy because of their innate capacity to target malignant cells, and ability to be transferred between donors and patients. However, since not all NK cells are equally effective at targeting cancer, selecting the right donor for cellular therapy is critical for the success of the treatment. Recently, cellular therapies utilising NK cells from cytomegalovirus (CMV)‐seropositive donors have been explored. However, whether these NK cells are the best source to treat paediatric acute lymphoblastic leukaemia (ALL) remains unclear. METHODS: Using a panel of patient‐derived paediatric B‐ and T‐ALL, we assessed the ability of NK cells from 49 healthy donors to mount an effective functional response against these two major subtypes of ALL. RESULTS: From this cohort, we have identified a pool of donors with superior activity against multiple ALL cells. While these donors were more likely to be CMV(+), we identified multiple CMV(neg) donors within this group. Furthermore, NK cells from these donors recognised B‐ and T‐ALL through different activating receptors. Dividing functional NK cells into 29 unique subsets, we observed that within each individual the same NK cell subsets dominated across all ALL cells. Intriguingly, this occurred despite the ALL cells in our panel expressing different combinations of NK cell ligands. Finally, we can demonstrate that cellular therapy products derived from these superior donors significantly delayed leukaemia progression in preclinical models of ALL. CONCLUSIONS: We have identified a pool of superior donors that are effective against a range of ALL cells, representing a potential pool of donors that can be used as an adoptive NK cell therapy to treat paediatric ALL. |
format | Online Article Text |
id | pubmed-7365579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73655792020-07-20 Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia Foley, Bree Ta, Clara Barnes, Samantha de Jong, Emma Nguyen, Michelle Cheung, Laurence C Buzzai, Anthony Wagner, Teagan Wylie, Ben Fernandez, Sonia Cruickshank, Mark Endersby, Raelene Kees, Ursula Waithman, Jason Clin Transl Immunology Original Articles OBJECTIVES: Natural killer (NK) cells are an attractive source of cells for an ‘off the shelf’ cellular therapy because of their innate capacity to target malignant cells, and ability to be transferred between donors and patients. However, since not all NK cells are equally effective at targeting cancer, selecting the right donor for cellular therapy is critical for the success of the treatment. Recently, cellular therapies utilising NK cells from cytomegalovirus (CMV)‐seropositive donors have been explored. However, whether these NK cells are the best source to treat paediatric acute lymphoblastic leukaemia (ALL) remains unclear. METHODS: Using a panel of patient‐derived paediatric B‐ and T‐ALL, we assessed the ability of NK cells from 49 healthy donors to mount an effective functional response against these two major subtypes of ALL. RESULTS: From this cohort, we have identified a pool of donors with superior activity against multiple ALL cells. While these donors were more likely to be CMV(+), we identified multiple CMV(neg) donors within this group. Furthermore, NK cells from these donors recognised B‐ and T‐ALL through different activating receptors. Dividing functional NK cells into 29 unique subsets, we observed that within each individual the same NK cell subsets dominated across all ALL cells. Intriguingly, this occurred despite the ALL cells in our panel expressing different combinations of NK cell ligands. Finally, we can demonstrate that cellular therapy products derived from these superior donors significantly delayed leukaemia progression in preclinical models of ALL. CONCLUSIONS: We have identified a pool of superior donors that are effective against a range of ALL cells, representing a potential pool of donors that can be used as an adoptive NK cell therapy to treat paediatric ALL. John Wiley and Sons Inc. 2020-07-16 /pmc/articles/PMC7365579/ /pubmed/32695339 http://dx.doi.org/10.1002/cti2.1151 Text en © 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Foley, Bree Ta, Clara Barnes, Samantha de Jong, Emma Nguyen, Michelle Cheung, Laurence C Buzzai, Anthony Wagner, Teagan Wylie, Ben Fernandez, Sonia Cruickshank, Mark Endersby, Raelene Kees, Ursula Waithman, Jason Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title | Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title_full | Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title_fullStr | Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title_full_unstemmed | Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title_short | Identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric B‐ and T‐cell acute lymphoblastic leukaemia |
title_sort | identifying the optimal donor for natural killer cell adoptive therapy to treat paediatric b‐ and t‐cell acute lymphoblastic leukaemia |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365579/ https://www.ncbi.nlm.nih.gov/pubmed/32695339 http://dx.doi.org/10.1002/cti2.1151 |
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