1. A Comprehensive Analysis of Primary Acute Myeloid Leukemia Identifies Biomarkers Predicting Susceptibility to Human Allogeneic Vγ9Vδ2 T Cells
- Author
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Martin Wilhelm, S Gundermann, Brigitte Kimmel, E Klinker, U Flierl, Hermann Einsele, and Kunzmann
- Subjects
Adult ,Cytotoxicity, Immunologic ,Male ,Cancer Research ,Myeloid ,T-Lymphocytes ,T cell ,medicine.medical_treatment ,Immunology ,Graft vs Leukemia Effect ,GPI-Linked Proteins ,Immunotherapy, Adoptive ,Cancer immunotherapy ,Antigen ,HLA Antigens ,Predictive Value of Tests ,hemic and lymphatic diseases ,medicine ,Humans ,Transplantation, Homologous ,Immunology and Allergy ,neoplasms ,Cells, Cultured ,Aged ,Aged, 80 and over ,Pharmacology ,business.industry ,Intracellular Signaling Peptides and Proteins ,Myeloid leukemia ,Receptors, Antigen, T-Cell, gamma-delta ,Immunotherapy ,Middle Aged ,Prognosis ,medicine.disease ,Transplantation ,Leukemia, Myeloid, Acute ,Leukemia ,medicine.anatomical_structure ,Histocompatibility ,Female ,business - Abstract
Allogeneic innate lymphocytes such as Vγ9Vδ2 T cells are attractive candidates for cancer immunotherapy as they provide MHC-unrestricted antitumor activity without clinical evidence for inducing graft-versus-host disease (GvHD). However, current cellular immunotherapy approaches lack predictive biomarkers identifying patient cohorts most susceptible to immune attack. For this purpose we performed a comprehensive analysis of clinical, genetic, metabolic, and immunophenotypic features of 19 primary acute myeloid leukemia (AML) samples and correlated these factors with AML blast recognition by allogeneic Vγ9Vδ2 T cells. We show that 36% of primary AML samples were intrinsically susceptible to allogeneic Vγ9Vδ2 T cells. Among several evaluated features, only UL-16 binding protein 1 (ULBP1) expression (P
- Published
- 2014
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