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

• Published in: Vaccines (Basel) 2024-01, Vol.12 (2), p.112
• Main Authors: 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
• Format: Article
• Language: English
• Subjects: Air cleanliness; Antigens; Batch production; CD8 antigen; Cell proliferation; cell therapy medicinal products (CTMP); Cervical cancer; clinical trial; Clinical trials; Composition; Cryopreservation; Cytokines; Dendritic cells; Flow cytometry; Growth; Health aspects; Human papillomavirus; Immunological adjuvants; Immunotherapy; Informed consent; large-scale dendritic cell production; Leukapheresis; Lymphocytes; Lymphocytes T; Patients; Phenotypes; Quality control; Radiation therapy; Testing; γ-Interferon
• ISSN: 2076-393X; 2076-393X
• DOI: 10.3390/vaccines12020112

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 ( value-0.0002). Tracking the viability and phenotype of cryopreserved MDCs showed a >90% viability for up to three years, while a mature DC phenotype was retained for up to one year. Our results confirm that the manual/semi-automated protocol was simple, consistent, and cost-effective, without the requirement for expensive equipment and without compromising on the quality of the final product.