Membrane-bound IL-15 co-expression powers a potent and persistent CD70-targeted TRuC T-cell therapy

These findings characterize ADP-520 as a first-in-class, CD70-targeted, fratricide-resistant autologous TRuC T-cell therapy leveraging native TCR signaling combined with constitutive IL-15 signaling to impart T cells with enhanced persistence, tumor penetration, and antitumor efficacy. This makes ADP-520 a promising cell immunotherapy candidate for clinical development, with the potential to overcome hurdles intrinsic to the treatment of solid tumors.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-05-30
DOI
https://doi.org/10.3389/fimmu.2025.1609658
Citations
3
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
3.14
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article

Membrane-bound IL-15 co-expression powers a potent and persistent CD70-targeted TRuC T-cell therapy

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3 citations
Frontiers in Immunology
CAR-T cell therapy research
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article

Membrane-bound IL-15 co-expression powers a potent and persistent CD70-targeted TRuC T-cell therapy

Lindsay Webb, Jason Lajoie, Adam Zieba, Amy Watt, Troy Patterson, Robert M. Tighe, Michael Lofgren, Erica Liu, Jian Ding, Michelle Fleury
article en
3 citations

Abstract

These findings characterize ADP-520 as a first-in-class, CD70-targeted, fratricide-resistant autologous TRuC T-cell therapy leveraging native TCR signaling combined with constitutive IL-15 signaling to impart T cells with enhanced persistence, tumor penetration, and antitumor efficacy. This makes ADP-520 a promising cell immunotherapy candidate for clinical development, with the potential to overcome hurdles intrinsic to the treatment of solid tumors.

Frontiers in ImmunologyVol. 16
Fulcrum Therapeutics (United States) (US), Adaptimmune (United Kingdom) (GB)
Openalex Percentile: Top 8%
CAR-T cell therapy research
3.14
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