Immuno‐Packed T‐Cell‐Fusogenic Liposome Empowers Adoptive T Cell Therapy for Solid Tumor Treatment (Adv. Mater. 8/2026)

IMPACTFUL Adoptive T Cell Therapy In their Research Article (DOI: 10.1002/adma.202510842), Mingqiang Li, Yu Tao, Haochen Yao, and co-workers present an immuno-packed T-cell-fusogenic liposome (IMPACTFUL) that enables T-cell engineering through membrane fusion. This approach facilitates concurrent targeting across multiple cellular compartments, including the cell membrane and cytoplasm. By leveraging this dual-targeting strategy, T cells acquire enhanced functionalities, such as improved tumor infiltration, overcoming immune tolerance, and reversing the immunosuppressive tumor microenvironment. This versatile platform offers a promising approach to enhance the therapeutic efficacy of adoptive T cell therapies for solid tumors.

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Publication Details

Journal
Advanced Materials
Published
2026-02-01
DOI
https://doi.org/10.1002/adma.72147
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
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article

Immuno‐Packed T‐Cell‐Fusogenic Liposome Empowers Adoptive T Cell Therapy for Solid Tumor Treatment (Adv. Mater. 8/2026)

Ke Yi, Huimin KONG, Qingguo Zhong, Enguo Ju et al.
Advanced Materials
CAR-T cell therapy research
article

Immuno‐Packed T‐Cell‐Fusogenic Liposome Empowers Adoptive T Cell Therapy for Solid Tumor Treatment (Adv. Mater. 8/2026)

Ke Yi, Huimin KONG, Qingguo Zhong, Enguo Ju, Tao Yu, Yun Liu, Haochen Yao, Yongkang Du, Chunxiong Zheng, Yeh‐Hsing Lao
article en

Abstract

IMPACTFUL Adoptive T Cell Therapy In their Research Article (DOI: 10.1002/adma.202510842), Mingqiang Li, Yu Tao, Haochen Yao, and co-workers present an immuno-packed T-cell-fusogenic liposome (IMPACTFUL) that enables T-cell engineering through membrane fusion. This approach facilitates concurrent targeting across multiple cellular compartments, including the cell membrane and cytoplasm. By leveraging this dual-targeting strategy, T cells acquire enhanced functionalities, such as improved tumor infiltration, overcoming immune tolerance, and reversing the immunosuppressive tumor microenvironment. This versatile platform offers a promising approach to enhance the therapeutic efficacy of adoptive T cell therapies for solid tumors.

Advanced MaterialsVol. 38(8)
Union Hospital (HK), Sun Yat-sen University (CN), South China Normal University (CN), Third Affiliated Hospital of Sun Yat-sen University (CN), Union Hospital (CN), University at Buffalo, State University of New York (US)
Openalex Percentile: Top 63%
CAR-T cell therapy research
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