Non-invasive cell-tracking methods for adoptive T cell therapies

Jelter Van Hoeck1, Christian Vanhove2, Stefaan C De Smedt1

  • 1Ghent Research Group on Nanomedicines, Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmaceutical Sciences, Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Drug Discovery Today
|October 31, 2021
PubMed

Insights

Adoptive T cell therapies (ACT) show promise but face challenges. In vivo cell-tracking offers non-invasive monitoring to improve patient management and overcome hurdles in solid tumors.

Area of Science:

  • Immunology
  • Biomedical Engineering
  • Oncology

Background:

  • Adoptive T cell therapies (ACT) have achieved success in hematologic malignancies and melanoma.
  • Significant challenges remain, including high costs, severe adverse events, and limited efficacy in solid tumors.

Purpose of the Study:

  • To review the principles and potential of in vivo cell-tracking for adoptive T cell therapies.
  • To discuss clinically relevant labeling strategies and their application in ACT.

Main Methods:

  • Review of existing literature on in vivo cell-tracking techniques.
  • Analysis of labeling strategies for T cells used in adoptive cell therapy.
  • Discussion of the clinical implications of cell-tracking in patient management.

Main Results:

  • In vivo cell-tracking enables real-time, non-invasive monitoring of T cell distribution, tumor homing, persistence, and organ redistribution.
  • Cell-tracking can facilitate early detection of non-responders and adverse events.
  • Various labeling strategies exist with potential clinical relevance for ACT.

Conclusions:

  • In vivo cell-tracking is a valuable tool for monitoring and managing patients undergoing ACT.
  • Addressing challenges in cell-tracking and labeling is crucial for expanding ACT applicability, especially in solid tumors.
  • Further development and clinical integration of cell-tracking technologies can enhance the safety and efficacy of ACT.

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