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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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