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Article: Optimization and Validation of a Harmonized Protocol for Generating Therapeutic-Grade Dendritic Cells in a Randomized Phase II Clinical Trial, Using Two Varied Antigenic Sources.

Seetharaman, Abirami / Christopher, Vasanth / Dhandapani, Hemavathi / Jayakumar, Hascitha / Dhanushkodi, Manikandan / Bhaskaran, Narmadha / Rajaraman, Swaminathan / Ranganathan, Rama / Sunder Singh, Shirley / Vijayakumar, Varalakshmi / Rajamanickam, Arivazhagan / Suri, Anil / Jagadish, Nirmala / Rajkumar, Thangarajan / Ramanathan, Priya

Vaccines

2024  Volume 12, Issue 2

Abstract: Autologous dendritic cell (DC)-based immunotherapy is a cell-based advanced therapy medicinal product (ATMP) that was first introduced more than three decades ago. In the current study, our objective was to establish a harmonized protocol using two ... ...

Abstract Autologous dendritic cell (DC)-based immunotherapy is a cell-based advanced therapy medicinal product (ATMP) that was first introduced more than three decades ago. In the current study, our objective was to establish a harmonized protocol using two varied antigenic sources and a good manufacturing practice (GMP)-compliant, manual method for generating clinical-grade DCs at a limited-resource academic setting. After obtaining ethical committee-approved informed consent, the recruited patients underwent leukapheresis, and single-batch DC production was carried out. Using responder-independent flow cytometric assays as quality control (QC) criteria, we propose a differentiation and maturation index (DI and MI, respectively), calculated with the QC cut-off and actual scores of each batch for comparison. Changes during cryopreservation and personnel variation were assessed periodically for up to two to three years. Using our harmonized batch production protocol, the average DI was 1.39 and MI was 1.25. Allogenic responder proliferation was observed in all patients, while IFN-gamma secretion, evaluated using flow cytometry, was detected in 10/36 patients and significantly correlated with CD8+ T cell proliferation (
Language English
Publishing date 2024-01-23
Publishing country Switzerland
Document type Journal Article
ZDB-ID 2703319-3
ISSN 2076-393X
ISSN 2076-393X
DOI 10.3390/vaccines12020112
Database MEDical Literature Analysis and Retrieval System OnLINE

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