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瘤内注射和保留有望改善癌症的细胞因子疗法。

Intratumoral injection and retention hold promise to improve cytokine therapies for cancer.

作者信息

Sauer Karsten, Rakhra Kavya, Wu Kaida, Mehta Naveen K, Michaelson Jennifer S, Baeuerle Patrick A

机构信息

Cullinan Therapeutics, Cambridge, MA, United States.

Institute of Immunology, Ludwig Maximilians Universitaet Muenchen, Planegg, Germany.

出版信息

Front Oncol. 2024 Aug 26;14:1456658. doi: 10.3389/fonc.2024.1456658. eCollection 2024.


DOI:10.3389/fonc.2024.1456658
PMID:39252938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11381304/
Abstract

As powerful activators of the immune system, cytokines have been extensively explored for treating various cancers. But despite encouraging advances and some drug approvals, the broad adoption of cytokine therapies in the clinic has been limited by low response rates and sometimes severe toxicities. This in part reflects an inefficient biodistribution to tumors or a pleiotropic action on bystander cells and tissues. Here, we first review these issues and then argue for the intratumoral delivery of engineered cytokine fusion proteins that have been optimized for tumor retention as a potential solution to overcome these limitations and realize the potential of cytokines as highly effective therapeutics for cancer.

摘要

作为免疫系统的强大激活剂,细胞因子已被广泛研究用于治疗各种癌症。尽管取得了令人鼓舞的进展并获得了一些药物批准,但细胞因子疗法在临床上的广泛应用受到低反应率和有时严重毒性的限制。这在一定程度上反映了其对肿瘤的生物分布效率低下,或对旁观者细胞和组织的多效性作用。在这里,我们首先回顾这些问题,然后论证肿瘤内递送经过优化以保留在肿瘤中的工程化细胞因子融合蛋白,作为克服这些限制并实现细胞因子作为癌症高效治疗药物潜力的潜在解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9db/11381304/e2c0792acbe6/fonc-14-1456658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9db/11381304/e2c0792acbe6/fonc-14-1456658-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9db/11381304/e2c0792acbe6/fonc-14-1456658-g001.jpg

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[1]
Intratumoral injection and retention hold promise to improve cytokine therapies for cancer.

Front Oncol. 2024-8-26

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本文引用的文献

[1]
Tumor-Localized Interleukin-2 and Interleukin-12 Combine with Radiation Therapy to Safely Potentiate Regression of Advanced Malignant Melanoma in Pet Dogs.

Clin Cancer Res. 2024-9-13

[2]
CLN-617 Retains IL2 and IL12 in Injected Tumors to Drive Robust and Systemic Immune-Mediated Antitumor Activity.

Cancer Immunol Res. 2024-8-1

[3]
Strategies to therapeutically modulate cytokine action.

Nat Rev Drug Discov. 2023-10

[4]
Spatiotemporally programming cytokine immunotherapies through protein engineering.

Immunol Rev. 2023-11

[5]
A systematic review of interleukin-2-based immunotherapies in clinical trials for cancer and autoimmune diseases.

EBioMedicine. 2023-4

[6]
Therapy with oncolytic viruses: progress and challenges.

Nat Rev Clin Oncol. 2023-3

[7]
A Review of the Abscopal Effect in the Era of Immunotherapy.

Cureus. 2022-9-26

[8]
PD-1 combination therapy with IL-2 modifies CD8 T cell exhaustion program.

Nature. 2022-10

[9]
Emerging principles of cytokine pharmacology and therapeutics.

Nat Rev Drug Discov. 2023-1

[10]
Current clinical landscape of oncolytic viruses as novel cancer immunotherapeutic and recent preclinical advancements.

Front Immunol. 2022

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