Adoptively transferred macrophages for cancer immunotherapy

Owing to their inherent ability to home to and infiltrate inflamed tissues, macrophage-based cancer immunotherapies exhibited a unique in vivo trafficking behavior, efficiently reaching and persisting within tumors. Macrophages orchestrated a multiarmed immune attack led by CD8+T cells, with the potential for local, intratumoral activation of effector cells, demonstrating a novel cancer immunotherapy platform with meaningfully different characteristics than clinically evaluated alternatives.

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Publication Details

Journal
Journal for ImmunoTherapy of Cancer
Published
2025-05-01
DOI
https://doi.org/10.1136/jitc-2024-010437
Citations
3
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
2.39
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Adoptively transferred macrophages for cancer immunotherapy

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Journal for ImmunoTherapy of Cancer
Immunotherapy and Immune Responses
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Adoptively transferred macrophages for cancer immunotherapy

Kyong Soo Park, Vineeth Chandran Suja, Supriya Prakash, Morgan E. Janes, Neha Kapate, Alexander P. Gottlieb, Samir Mitragotri, Liwen Wang, Jennifer L. Guerriero
article en
3 citations

Abstract

Owing to their inherent ability to home to and infiltrate inflamed tissues, macrophage-based cancer immunotherapies exhibited a unique in vivo trafficking behavior, efficiently reaching and persisting within tumors. Macrophages orchestrated a multiarmed immune attack led by CD8+T cells, with the potential for local, intratumoral activation of effector cells, demonstrating a novel cancer immunotherapy platform with meaningfully different characteristics than clinically evaluated alternatives.

Journal for ImmunoTherapy of CancerVol. 13(5)
Brigham and Women's Hospital (US), Harvard University (US), Harvard–MIT Division of Health Sciences and Technology (US), Dana-Farber/Harvard Cancer Center (US), Dana-Farber Brigham Cancer Center (US), Massachusetts Institute of Technology (US)
Good health and well-being
Openalex Percentile: Top 11%
Immunotherapy and Immune Responses
2.39
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