Identification of Anti-tumor Cells Carrying Natural Killer (NK) Cell Antigens in Patients With Hematological Cancers
Ewelina Krzywinska,
Nerea Allende-Vega,
Amelie Cornillon,
Dang-Nghiem Vo,
Laure Cayrefourcq,
Catherine Panabieres,
Carlos Vilches,
Julie Déchanet-Merville,
Yosr Hicheri,
Jean-François Rossi,
Guillaume Cartron,
Martin Villalba
Affiliations
Ewelina Krzywinska
INSERM U1183, Université de Montpellier, UFR Médecine, Montpellier, France
Nerea Allende-Vega
INSERM U1183, Université de Montpellier, UFR Médecine, Montpellier, France
Amelie Cornillon
INSERM U1183, Université de Montpellier, UFR Médecine, Montpellier, France
Dang-Nghiem Vo
INSERM U1183, Université de Montpellier, UFR Médecine, Montpellier, France
Laure Cayrefourcq
Laboratory of Rare Human Circulating Cells (LCCRH), Department of Cellular and Tissular Biopathology of Tumors, University Medical Centre, Montpellier, France
Catherine Panabieres
Laboratory of Rare Human Circulating Cells (LCCRH), Department of Cellular and Tissular Biopathology of Tumors, University Medical Centre, Montpellier, France
Carlos Vilches
Inmunogenética-HLA, Hospital Univ. Puerta de Hierro, Manuel de Falla 1, 28220 Majadahonda, Madrid, Spain
Julie Déchanet-Merville
CNRS UMR 5164, Université Bordeaux, 33076 Bordeaux, France
Yosr Hicheri
Département d'Hématologie Clinique, CHU Montpellier, Université Montpellier, 80 Avenue Augustin Fliche, 34295 Montpellier, France
Jean-François Rossi
Département d'Hématologie Clinique, CHU Montpellier, Université Montpellier, 80 Avenue Augustin Fliche, 34295 Montpellier, France
Guillaume Cartron
Département d'Hématologie Clinique, CHU Montpellier, Université Montpellier, 80 Avenue Augustin Fliche, 34295 Montpellier, France
Martin Villalba
INSERM U1183, Université de Montpellier, UFR Médecine, Montpellier, France
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 CD56dimCD16+ 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.