Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/139674
Title: Immune response generated with the administration of autologous dendritic cells pulsed with an allogenic tumoral cell lines lysate in patients with newly diagnosed DIPG.
Author: Benítez-Ribas, Daniel
Cabezón Cabello, Raquel
Flórez Grau, Georgina
Molero, Mari Carmen
Puerta, Patricia
Guillen, Antonio
González Navarro, E. Azucena
Paco, Sonia
Carcaboso, Angel M.
Santa-Maria Lopez, Vicente
Cruz Martínez, Ofelia
Torres, Carmen de
Salvador, Noelia
Juan, Manel
Mora, Jaume
Morales La Madrid, Andres
Keywords: Immunoteràpia
Tumors
Vacunació
Cèl·lules dendrítiques
Immunotheraphy
Tumors
Vaccination
Dendritic cells
Issue Date: 26-Apr-2018
Publisher: Frontiers Media
Abstract: Background and objective. Diffuse intrinsic pontine glioma (DIPG) is a lethal brainstem tumor in children. Dendritic cells (DCs) have T-cell stimulatory capacity and, therefore, potential antitumor activity for disease control. DCs vaccines have been shown to reactivate tumor-specific T cells in both clinical and pre-clinical settings. We designed a phase Ib immunotherapy (IT) clinical trial with the use of autologous dendritic cells (ADCs) pulsed with an allogeneic tumors cell-lines lysate (ATCL) in patients with newly diagnosed DIPG after irradiation (RT). Methods. Nine patients with newly diagnosed DIPG met enrollment criteria. Autologous dendritic cell vaccines (ADCV) were prepared from monocytes obtained by leukapheresis. Five ADCV doses were administered intradermally during induction phase. In the absence of tumor progression, patients received 3 boosts of tumor lysate every three months during the maintenance phase. Results. Vaccine fabrication was feasible in all patients included in the study. Non-specific KLH (9/9 patients) and specific (8/9 patients) antitumor response was identified by immunologic studies in peripheral blood mononuclear cells (PBMC). Immunological responses were also confirmed in the T lymphocytes isolated from the cerebrospinal fluid (CSF) of 2 patients. Vaccine administration resulted safe in all patients treated with this schema. Conclusions. These preliminary results demonstrate that ADCV preparation is feasible, safe and generate a DIPG-specific immune response detected in PBMC and CSF. This strategy shows a promising backbone for future schemas of combination immunotherapy.
Note: Reproducció del document publicat a: https://doi.org/10.3389/fonc.2018.00127
It is part of: Frontiers in Oncology, 2018, vol. 8, p. 127
URI: http://hdl.handle.net/2445/139674
Related resource: https://doi.org/10.3389/fonc.2018.00127
ISSN: 2234-943X
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)

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