Determinants for Effective ALECSAT Immunotherapy Treatment on Autologous Patient-Derived Glioblastoma Stem Cells
Adult
Male
0301 basic medicine
Original article
Medicinska och farmaceutiska grundvetenskaper
Brain Neoplasms
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Basic Medicine
Fibroblasts
Middle Aged
Combined Modality Therapy
Immunotherapy, Adoptive
3. Good health
03 medical and health sciences
T-Lymphocyte Subsets
Cell Line, Tumor
Neoplastic Stem Cells
Humans
Female
Radiotherapy, Adjuvant
Lymphocyte Count
Glioblastoma
RC254-282
Aged
DOI:
10.1016/j.neo.2017.10.006
Publication Date:
2017-12-01T20:36:34Z
AUTHORS (10)
ABSTRACT
Glioblastoma (GBM) is the most aggressive primary brain tumor with a median survival of less than 15 months, emphasizing the need for better treatments. Immunotherapy as a treatment for improving or aiding the patient's own immune defense to target the tumor has been suggested for GBM. A randomized clinical trial of adoptive cell transfer using ALECSAT (Autologous Lymphoid Effector Cells Specific Against Tumor Cells) is currently ongoing in Sweden. Here we performed a paired pre-clinical study to investigate the composition and in vitro effect of ALECSAT and identify determinants for the effect using autologous GBM-derived cancer stem cells (CSC), immunocytochemistry and flow cytometry. We show a clear dose-response relationship of ALECSAT on CSC, suggesting that the number of infused cells is of importance. In addition, the in vitro effect of ALECSAT on CSC correlated significantly to the blood count of T helper (Th) cells in the patient indicating a potential benefit of collecting cells for ALECSAT preparation at an even earlier stage when patients generally have a better blood count. The factors identified in this study will be important to consider in the design of future immunotherapy trials to achieve prolonged survival.
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