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Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma

Few approaches have been made toward exploring autologous NK cells in settings of cancer immunotherapy. Here, we demonstrate the feasibility of infusing multiple doses of ex vivo activated and expanded autologous NK cells in patients with multiple myeloma (MM) post-autologous stem cell transplantati...

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Autores principales: Nahi, Hareth, Chrobok, Michael, Meinke, Stephan, Gran, Charlotte, Marquardt, Nicole, Afram, Gabriel, Sutlu, Tolga, Gilljam, Mari, Stellan, Birgitta, Wagner, Arnika K., Blomberg, Pontus, Holmqvist, Per-Henrik, Walther-Jallow, Lilian, Mellström, Karin, Liwing, Johan, Gustafsson, Charlotte, Månsson, Robert, Klimkowska, Monika, Gahrton, Gösta, Lund, Johan, Ljungman, Per, Ljunggren, Hans-Gustaf, Alici, Evren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861830/
https://www.ncbi.nlm.nih.gov/pubmed/35243416
http://dx.doi.org/10.1016/j.xcrm.2022.100508
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author Nahi, Hareth
Chrobok, Michael
Meinke, Stephan
Gran, Charlotte
Marquardt, Nicole
Afram, Gabriel
Sutlu, Tolga
Gilljam, Mari
Stellan, Birgitta
Wagner, Arnika K.
Blomberg, Pontus
Holmqvist, Per-Henrik
Walther-Jallow, Lilian
Mellström, Karin
Liwing, Johan
Gustafsson, Charlotte
Månsson, Robert
Klimkowska, Monika
Gahrton, Gösta
Lund, Johan
Ljungman, Per
Ljunggren, Hans-Gustaf
Alici, Evren
author_facet Nahi, Hareth
Chrobok, Michael
Meinke, Stephan
Gran, Charlotte
Marquardt, Nicole
Afram, Gabriel
Sutlu, Tolga
Gilljam, Mari
Stellan, Birgitta
Wagner, Arnika K.
Blomberg, Pontus
Holmqvist, Per-Henrik
Walther-Jallow, Lilian
Mellström, Karin
Liwing, Johan
Gustafsson, Charlotte
Månsson, Robert
Klimkowska, Monika
Gahrton, Gösta
Lund, Johan
Ljungman, Per
Ljunggren, Hans-Gustaf
Alici, Evren
author_sort Nahi, Hareth
collection PubMed
description Few approaches have been made toward exploring autologous NK cells in settings of cancer immunotherapy. Here, we demonstrate the feasibility of infusing multiple doses of ex vivo activated and expanded autologous NK cells in patients with multiple myeloma (MM) post-autologous stem cell transplantation. Infused NK cells were detected in circulation up to 4 weeks after the last infusion. Elevations in plasma granzyme B levels were observed following each consecutive NK cell infusion. Moreover, increased granzyme B levels were detected in bone marrow 4 weeks after the last infusion. All measurable patients had objective, detectable responses after NK cell infusions in terms of reduction in M-component and/or minimal residual disease. The present study demonstrates that autologous NK cell-based immunotherapy is feasible in a setting of MM consolidation therapy. It opens up the possibility for usage of autologous NK cells in clinical settings where patients are not readily eligible for allogeneic NK cell-based immunotherapies.
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spelling pubmed-88618302022-03-02 Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma Nahi, Hareth Chrobok, Michael Meinke, Stephan Gran, Charlotte Marquardt, Nicole Afram, Gabriel Sutlu, Tolga Gilljam, Mari Stellan, Birgitta Wagner, Arnika K. Blomberg, Pontus Holmqvist, Per-Henrik Walther-Jallow, Lilian Mellström, Karin Liwing, Johan Gustafsson, Charlotte Månsson, Robert Klimkowska, Monika Gahrton, Gösta Lund, Johan Ljungman, Per Ljunggren, Hans-Gustaf Alici, Evren Cell Rep Med Article Few approaches have been made toward exploring autologous NK cells in settings of cancer immunotherapy. Here, we demonstrate the feasibility of infusing multiple doses of ex vivo activated and expanded autologous NK cells in patients with multiple myeloma (MM) post-autologous stem cell transplantation. Infused NK cells were detected in circulation up to 4 weeks after the last infusion. Elevations in plasma granzyme B levels were observed following each consecutive NK cell infusion. Moreover, increased granzyme B levels were detected in bone marrow 4 weeks after the last infusion. All measurable patients had objective, detectable responses after NK cell infusions in terms of reduction in M-component and/or minimal residual disease. The present study demonstrates that autologous NK cell-based immunotherapy is feasible in a setting of MM consolidation therapy. It opens up the possibility for usage of autologous NK cells in clinical settings where patients are not readily eligible for allogeneic NK cell-based immunotherapies. Elsevier 2022-01-28 /pmc/articles/PMC8861830/ /pubmed/35243416 http://dx.doi.org/10.1016/j.xcrm.2022.100508 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nahi, Hareth
Chrobok, Michael
Meinke, Stephan
Gran, Charlotte
Marquardt, Nicole
Afram, Gabriel
Sutlu, Tolga
Gilljam, Mari
Stellan, Birgitta
Wagner, Arnika K.
Blomberg, Pontus
Holmqvist, Per-Henrik
Walther-Jallow, Lilian
Mellström, Karin
Liwing, Johan
Gustafsson, Charlotte
Månsson, Robert
Klimkowska, Monika
Gahrton, Gösta
Lund, Johan
Ljungman, Per
Ljunggren, Hans-Gustaf
Alici, Evren
Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title_full Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title_fullStr Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title_full_unstemmed Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title_short Autologous NK cells as consolidation therapy following stem cell transplantation in multiple myeloma
title_sort autologous nk cells as consolidation therapy following stem cell transplantation in multiple myeloma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861830/
https://www.ncbi.nlm.nih.gov/pubmed/35243416
http://dx.doi.org/10.1016/j.xcrm.2022.100508
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