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Clinical-scale, modular manufacturing of tumor-reactive TILs using a closed and automated culture system.

Christina Völzke ,
Lisa Ehrhardt ,
Laura Fischer ,
Peter Maul ,
Carina Wenzel ,
Arina Riabinska ,
Elvira Criado-Moronati ,
Mike Dienstbier ,
Jessica Hassel ,
Danmei Zhang ,
John B Haanen ,
Rupert Handgretinger ,
Ian R Hardy ,
Bianca Heemskerk ,
Andrzej Dzionek

Abstract

Recent studies have revealed the potential of tumor-infiltrating lymphocytes (TILs) to treat solid tumors effectively and safely. However, the translation of TIL therapy for patients is still hampered by non-standardized and laborious manufacturing procedures that are expensive and produce highly variable cellular products. To address these limitations, the CliniMACS Prodigy® Tumor Reactive T cell (TRT) Process has been developed. The TRT Process allows the automated isolation, transduction, and expansion of tumor-reactive T cells in a clinically compliant and closed system under GMP conditions. The TRT Process can generate tumor-reactive T cells using several methodologies which reflect clinically relevant applications. It can manage an automated Rapid Expansion Protocol (REP) using GMP-compliant reagents to generate a TIL cell product from solid tumors, including melanoma. Additionally, the TRT Process automates the closed selection of CD137-expressing TILs directly from tumor digest followed by the direct expansion of selected cells. Enriched CD137+ TILs could be robustly expanded even when as few as 1x104 TILs were used to seed the REP phase. These data provide proof-of-concept for the isolation and expansion of tumor-reactive T cells from tumor digest in a closed, automated manner in the CliniMACS Prodigy, allowing for an efficient, simple, and reproducible manufacturing of TIL products. The direct selection of CD137+ TILs from tumor digest removes the need for the pre-REP phase, selects for therapeutically relevant cells, and can dramatically shorten the manufacturing time compared to conventional methods.

More about this publication

Frontiers in immunology

Volume 15
Pages 1483254
Publication date 24-12-2024

Full text links

Publisher website (DOI) 10.3389/fimmu.2024.1483254
Europe PubMed Central 39717766
Pubmed 39717766

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