Frontiers in Immunology (Dec 2024)

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,
  • John B. Haanen,
  • John B. Haanen,
  • Rupert Handgretinger,
  • Ian R. Hardy,
  • Bianca Heemskerk,
  • Andrzej Dzionek

DOI
https://doi.org/10.3389/fimmu.2024.1483254
Journal volume & issue
Vol. 15

Abstract

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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.

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