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Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers

Natural killer (NK) cells, a cytotoxic lymphocyte lineage, are able to kill tumor cells in vitro and in mouse models. However, whether these cells display an anti-tumor activity in cancer patients has not been demonstrated. Here we have addressed this issue in patients with several hematological can...

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Autores principales: Krzywinska, Ewelina, Allende-Vega, Nerea, Cornillon, Amelie, Vo, Dang-Nghiem, Cayrefourcq, Laure, Panabieres, Catherine, Vilches, Carlos, Déchanet-Merville, Julie, Hicheri, Yosr, Rossi, Jean-François, Cartron, Guillaume, Villalba, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634619/
https://www.ncbi.nlm.nih.gov/pubmed/26629531
http://dx.doi.org/10.1016/j.ebiom.2015.08.021
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author Krzywinska, Ewelina
Allende-Vega, Nerea
Cornillon, Amelie
Vo, Dang-Nghiem
Cayrefourcq, Laure
Panabieres, Catherine
Vilches, Carlos
Déchanet-Merville, Julie
Hicheri, Yosr
Rossi, Jean-François
Cartron, Guillaume
Villalba, Martin
author_facet Krzywinska, Ewelina
Allende-Vega, Nerea
Cornillon, Amelie
Vo, Dang-Nghiem
Cayrefourcq, Laure
Panabieres, Catherine
Vilches, Carlos
Déchanet-Merville, Julie
Hicheri, Yosr
Rossi, Jean-François
Cartron, Guillaume
Villalba, Martin
author_sort Krzywinska, Ewelina
collection PubMed
description Natural killer (NK) cells, a cytotoxic lymphocyte lineage, are able to kill tumor cells in vitro and in mouse models. However, whether these cells display an anti-tumor activity in cancer patients has not been demonstrated. Here we have addressed this issue in patients with several hematological cancers. We found a population of highly activated CD56(dim)CD16(+) NK cells that have recently degranulated, evidence of killing activity, and it is absent in healthy donors. A high percentage of these cells expressed natural killer cell p46-related protein (NKp46), natural-killer group 2, member D (NKG2D) and killer inhibitory receptors (KIRs) and a low percentage expressed NKG2A and CD94. They are also characterized by a high metabolic activity and active proliferation. Notably, we found that activated NK cells from hematological cancer patients have non-NK tumor cell antigens on their surface, evidence of trogocytosis during tumor cell killing. Finally, we found that these activated NK cells are distinguished by their CD45RA(+)RO(+) phenotype, as opposed to non-activated cells in patients or in healthy donors displaying a CD45RA(+)RO(−) phenotype similar to naïve T cells. In summary, we show that CD45RA(+)RO(+) cells, which resemble a unique NK population, have recognized tumor cells and degranulate in patients with hematological neoplasias.
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spelling pubmed-46346192015-12-01 Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers Krzywinska, Ewelina Allende-Vega, Nerea Cornillon, Amelie Vo, Dang-Nghiem Cayrefourcq, Laure Panabieres, Catherine Vilches, Carlos Déchanet-Merville, Julie Hicheri, Yosr Rossi, Jean-François Cartron, Guillaume Villalba, Martin EBioMedicine Research Article Natural killer (NK) cells, a cytotoxic lymphocyte lineage, are able to kill tumor cells in vitro and in mouse models. However, whether these cells display an anti-tumor activity in cancer patients has not been demonstrated. Here we have addressed this issue in patients with several hematological cancers. We found a population of highly activated CD56(dim)CD16(+) NK cells that have recently degranulated, evidence of killing activity, and it is absent in healthy donors. A high percentage of these cells expressed natural killer cell p46-related protein (NKp46), natural-killer group 2, member D (NKG2D) and killer inhibitory receptors (KIRs) and a low percentage expressed NKG2A and CD94. They are also characterized by a high metabolic activity and active proliferation. Notably, we found that activated NK cells from hematological cancer patients have non-NK tumor cell antigens on their surface, evidence of trogocytosis during tumor cell killing. Finally, we found that these activated NK cells are distinguished by their CD45RA(+)RO(+) phenotype, as opposed to non-activated cells in patients or in healthy donors displaying a CD45RA(+)RO(−) phenotype similar to naïve T cells. In summary, we show that CD45RA(+)RO(+) cells, which resemble a unique NK population, have recognized tumor cells and degranulate in patients with hematological neoplasias. Elsevier 2015-08-13 /pmc/articles/PMC4634619/ /pubmed/26629531 http://dx.doi.org/10.1016/j.ebiom.2015.08.021 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Krzywinska, Ewelina
Allende-Vega, Nerea
Cornillon, Amelie
Vo, Dang-Nghiem
Cayrefourcq, Laure
Panabieres, Catherine
Vilches, Carlos
Déchanet-Merville, Julie
Hicheri, Yosr
Rossi, Jean-François
Cartron, Guillaume
Villalba, Martin
Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title_full Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title_fullStr Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title_full_unstemmed Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title_short Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
title_sort identification of anti-tumor cells carrying natural killer (nk) cell antigens in patients with hematological cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634619/
https://www.ncbi.nlm.nih.gov/pubmed/26629531
http://dx.doi.org/10.1016/j.ebiom.2015.08.021
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