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Nano-immunotherapy: Merging immunotherapy precision with nanomaterial delivery.

作者信息

Ngo Thu Ha, Menon Soumya, Rivero-Müller Adolfo

机构信息

Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.

出版信息

iScience. 2025 Mar 30;28(5):112319. doi: 10.1016/j.isci.2025.112319. eCollection 2025 May 16.


DOI:10.1016/j.isci.2025.112319
PMID:40292310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12033950/
Abstract

In current landscape of cancer treatment, nanotherapy and cellular therapy stand out as promising and innovative approaches. Nanotherapy have excelled in delivering functional molecules effectively to target cancer cells, however the targetability is mostly the result of the enhanced permeability and retention effect. Meanwhile, cellular therapies such recently emerging chimeric antigen receptor (CAR)-T therapy are proficient at specifically targeting cancer cells by using engineered receptors on T cells. Yet, cellular therapies preform poor in solid tumors due to immunosuppression and cancer cell resistance to immuno-stimulation, in other words their delivery of deadly cargo is deficient. Therefore, combining nanotherapy and immunotherapy is an emerging trend, with ongoing clinical trials exploring their synergistic effects. This 2-input approach holds promise for enhancing treatment efficacy and overcoming limitations in cancer therapy. In this review, we will discuss two aspects: targetability and delivery for each individual therapy and what the combined nano-immunotherapy strategies have achieved up to now. In the last section, some future perspectives for this combination are suggested.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/2ffed8670b3f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/6dac4967652a/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/15bd224005bc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/e924742b7714/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/293d9719fca5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/b5b01f9b4f74/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/9a603fd90f49/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/5763e348f53b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/2ffed8670b3f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/6dac4967652a/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/15bd224005bc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/e924742b7714/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/293d9719fca5/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/b5b01f9b4f74/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/9a603fd90f49/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/5763e348f53b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7d/12033950/2ffed8670b3f/gr7.jpg

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[1]
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[2]
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[3]
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[6]
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[8]
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[10]
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引用本文的文献

[1]
Nano-enabled strategies for targeted immunotherapy in gastrointestinal cancers.

Front Immunol. 2025-8-14

本文引用的文献

[1]
10 years of BiTE immunotherapy: an overview with a focus on pancreatic cancer.

Front Oncol. 2024-12-20

[2]
Silver nanoparticle induced immunogenic cell death can improve immunotherapy.

J Nanobiotechnology. 2024-11-10

[3]
Glypican-3-targeted macrophages delivering drug-loaded exosomes offer efficient cytotherapy in mouse models of solid tumours.

Nat Commun. 2024-9-23

[4]
Programmed death receptor (PD-)1/PD-ligand (L)1 in urological cancers : the "all-around warrior" in immunotherapy.

Mol Cancer. 2024-9-2

[5]
PD1/PD-L1 blockade in clear cell renal cell carcinoma: mechanistic insights, clinical efficacy, and future perspectives.

Mol Cancer. 2024-7-16

[6]
Progresses of T-cell-engaging bispecific antibodies in treatment of solid tumors.

Int Immunopharmacol. 2024-9-10

[7]
Autologous patient-derived exhausted nano T-cells exploit tumor immune evasion to engage an effective cancer therapy.

Mol Cancer. 2024-5-9

[8]
CAR affinity modulates the sensitivity of CAR-T cells to PD-1/PD-L1-mediated inhibition.

Nat Commun. 2024-4-26

[9]
Targeting novel regulated cell death: Ferroptosis, pyroptosis and necroptosis in anti-PD-1/PD-L1 cancer immunotherapy.

Cell Prolif. 2024-8

[10]
Oncolytic mineralized bacteria as potent locally administered immunotherapeutics.

Nat Biomed Eng. 2024-5

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