Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia

<p>CD19-NKCEs efficiently promote NK-cell antileukemia activity in a transplantation setting. <b>A,</b> Evaluation of NKp46, NKp30, CD16, perforin, and granzyme B expression in NK cells from transplanted patients (Post1–3M; <i>n</i> = 12) and healthy donors (HD; <i&g...

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Главный автор: Natalia Colomar-Carando (14611340) (author)
Другие авторы: Laurent Gauthier (15129623) (author), Pietro Merli (15129626) (author), Fabrizio Loiacono (5306981) (author), Paolo Canevali (332990) (author), Michela Falco (368897) (author), Federica Galaverna (8825531) (author), Benjamin Rossi (15129629) (author), Frédéric Bosco (15129632) (author), Mélody Caratini (15129635) (author), Maria Cristina Mingari (8409327) (author), Franco Locatelli (15127797) (author), Eric Vivier (48284) (author), Raffaella Meazza (7179467) (author), Daniela Pende (15129638) (author)
Опубликовано: 2025
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_version_ 1849927631567323136
author Natalia Colomar-Carando (14611340)
author2 Laurent Gauthier (15129623)
Pietro Merli (15129626)
Fabrizio Loiacono (5306981)
Paolo Canevali (332990)
Michela Falco (368897)
Federica Galaverna (8825531)
Benjamin Rossi (15129629)
Frédéric Bosco (15129632)
Mélody Caratini (15129635)
Maria Cristina Mingari (8409327)
Franco Locatelli (15127797)
Eric Vivier (48284)
Raffaella Meazza (7179467)
Daniela Pende (15129638)
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Natalia Colomar-Carando (14611340)
Laurent Gauthier (15129623)
Pietro Merli (15129626)
Fabrizio Loiacono (5306981)
Paolo Canevali (332990)
Michela Falco (368897)
Federica Galaverna (8825531)
Benjamin Rossi (15129629)
Frédéric Bosco (15129632)
Mélody Caratini (15129635)
Maria Cristina Mingari (8409327)
Franco Locatelli (15127797)
Eric Vivier (48284)
Raffaella Meazza (7179467)
Daniela Pende (15129638)
author_role author
dc.creator.none.fl_str_mv Natalia Colomar-Carando (14611340)
Laurent Gauthier (15129623)
Pietro Merli (15129626)
Fabrizio Loiacono (5306981)
Paolo Canevali (332990)
Michela Falco (368897)
Federica Galaverna (8825531)
Benjamin Rossi (15129629)
Frédéric Bosco (15129632)
Mélody Caratini (15129635)
Maria Cristina Mingari (8409327)
Franco Locatelli (15127797)
Eric Vivier (48284)
Raffaella Meazza (7179467)
Daniela Pende (15129638)
dc.date.none.fl_str_mv 2025-11-25T13:42:39Z
dc.identifier.none.fl_str_mv 10.1158/2326-6066.30710194
dc.relation.none.fl_str_mv https://figshare.com/articles/figure/Figure_4_from_Exploiting_Natural_Killer_Cell_Engagers_to_Control_Pediatric_B-cell_Precursor_Acute_Lymphoblastic_Leukemia/30710194
dc.rights.none.fl_str_mv CC BY
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Cancer
Immuno-oncology
Hematological Cancers
Leukemias
Immunology
NK cells
Immunotherapy
Stem cell transplantation
dc.title.none.fl_str_mv Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
dc.type.none.fl_str_mv Image
Figure
info:eu-repo/semantics/publishedVersion
image
description <p>CD19-NKCEs efficiently promote NK-cell antileukemia activity in a transplantation setting. <b>A,</b> Evaluation of NKp46, NKp30, CD16, perforin, and granzyme B expression in NK cells from transplanted patients (Post1–3M; <i>n</i> = 12) and healthy donors (HD; <i>n</i> = 5–11). <b>B,</b> Representative experiment of cytototoxicity (7AAD/AnnV staining). MHH-CALL-4 or ALL#06 primary leukemia target cells were cultured either alone (only target) or with resting NK cells from a transplanted patient (3 months after haplo-HSCT) and the indicated NKCEs (10<sup>0</sup> μg/mL). Numbers indicate the percentage of cells in each quadrant. Percent of specific lysis (7AAD/AnnV staining; <b>C</b>) and CD107a degranulation of resting NK cells (<b>D</b>) from transplanted patients against MHH-CALL-4 (left) or primary leukemia blasts (ALL#04 and ALL#06; right) in the presence of the indicated NKCE at 10<sup>0</sup> μg/mL. Pooled data obtained with primary leukemia blasts are shown. Results from 5–8 independent experiments are reported. The incubation time for all the tests was 4 hours. Bar show mean ± SEM. Statistical significance: *, <i>P</i> ≤ 0.05; **, <i>P</i> ≤ 0.01; ***, <i>P</i> ≤ 0.001. Mann–Whitney test was used to calculate statistical differences.</p>
eu_rights_str_mv openAccess
id Manara_51edda2d78b5d2883c32afc479a13056
identifier_str_mv 10.1158/2326-6066.30710194
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30710194
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
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rights_invalid_str_mv CC BY
spelling Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic LeukemiaNatalia Colomar-Carando (14611340)Laurent Gauthier (15129623)Pietro Merli (15129626)Fabrizio Loiacono (5306981)Paolo Canevali (332990)Michela Falco (368897)Federica Galaverna (8825531)Benjamin Rossi (15129629)Frédéric Bosco (15129632)Mélody Caratini (15129635)Maria Cristina Mingari (8409327)Franco Locatelli (15127797)Eric Vivier (48284)Raffaella Meazza (7179467)Daniela Pende (15129638)CancerImmuno-oncologyHematological CancersLeukemiasImmunologyNK cellsImmunotherapyStem cell transplantation<p>CD19-NKCEs efficiently promote NK-cell antileukemia activity in a transplantation setting. <b>A,</b> Evaluation of NKp46, NKp30, CD16, perforin, and granzyme B expression in NK cells from transplanted patients (Post1–3M; <i>n</i> = 12) and healthy donors (HD; <i>n</i> = 5–11). <b>B,</b> Representative experiment of cytototoxicity (7AAD/AnnV staining). MHH-CALL-4 or ALL#06 primary leukemia target cells were cultured either alone (only target) or with resting NK cells from a transplanted patient (3 months after haplo-HSCT) and the indicated NKCEs (10<sup>0</sup> μg/mL). Numbers indicate the percentage of cells in each quadrant. Percent of specific lysis (7AAD/AnnV staining; <b>C</b>) and CD107a degranulation of resting NK cells (<b>D</b>) from transplanted patients against MHH-CALL-4 (left) or primary leukemia blasts (ALL#04 and ALL#06; right) in the presence of the indicated NKCE at 10<sup>0</sup> μg/mL. Pooled data obtained with primary leukemia blasts are shown. Results from 5–8 independent experiments are reported. The incubation time for all the tests was 4 hours. Bar show mean ± SEM. Statistical significance: *, <i>P</i> ≤ 0.05; **, <i>P</i> ≤ 0.01; ***, <i>P</i> ≤ 0.001. Mann–Whitney test was used to calculate statistical differences.</p>2025-11-25T13:42:39ZImageFigureinfo:eu-repo/semantics/publishedVersionimage10.1158/2326-6066.30710194https://figshare.com/articles/figure/Figure_4_from_Exploiting_Natural_Killer_Cell_Engagers_to_Control_Pediatric_B-cell_Precursor_Acute_Lymphoblastic_Leukemia/30710194CC BYinfo:eu-repo/semantics/openAccessoai:figshare.com:article/307101942025-11-25T13:42:39Z
spellingShingle Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
Natalia Colomar-Carando (14611340)
Cancer
Immuno-oncology
Hematological Cancers
Leukemias
Immunology
NK cells
Immunotherapy
Stem cell transplantation
status_str publishedVersion
title Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
title_full Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
title_fullStr Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
title_full_unstemmed Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
title_short Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
title_sort Figure 4 from Exploiting Natural Killer Cell Engagers to Control Pediatric B-cell Precursor Acute Lymphoblastic Leukemia
topic Cancer
Immuno-oncology
Hematological Cancers
Leukemias
Immunology
NK cells
Immunotherapy
Stem cell transplantation