Suppr超能文献

免疫调节细胞因子疗法的工程策略——挑战与临床进展

Engineering Strategies for Immunomodulatory Cytokine Therapies - Challenges and Clinical Progress.

作者信息

Pires Ivan S, Hammond Paula T, Irvine Darrell J

机构信息

Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main Street, Cambridge, Massachusetts 02142, United States.

出版信息

Adv Ther (Weinh). 2021 Aug;4(8). doi: 10.1002/adtp.202100035. Epub 2021 Apr 2.

Abstract

Cytokines are immunoregulatory proteins involved in many pathological states with promising potential as therapeutic agents. A diverse array of cytokines have been studied in preclinical disease models since the 1950s, some of which became successful biopharmaceutical products with the advancement of recombinant protein technology in the 1980s. However, following these early approvals, clinical translation of these natural immune signaling molecules has been limited due to their pleiotropic action in many cell types, and the fact that they have evolved to act primarily locally in tissues. These characteristics, combined with poor pharmacokinetics, have hindered the delivery of cytokines via systemic administration routes due to dose-limiting toxicities. However, given their clinical potential and recent clinical successes in cancer immunotherapy, cytokines continue to be extensively pursued in preclinical and clinical studies, and a range of molecular and formulation engineering strategies are being applied to reduce treatment toxicity while maintaining or enhancing therapeutic efficacy. This review provides a brief background on the characteristics of cytokines and their history as clinical therapeutics, followed by a deeper discussion on the engineering strategies developed for cytokine therapies with a focus on the translational relevance of these approaches.

摘要

细胞因子是参与多种病理状态的免疫调节蛋白,作为治疗药物具有广阔的潜力。自20世纪50年代以来,人们在临床前疾病模型中对各种各样的细胞因子进行了研究,其中一些随着20世纪80年代重组蛋白技术的进步成为了成功的生物制药产品。然而,在这些早期获批之后,由于这些天然免疫信号分子在许多细胞类型中具有多效性作用,且它们主要在组织中局部发挥作用,其临床转化受到了限制。这些特性,再加上药代动力学不佳,由于剂量限制性毒性,阻碍了通过全身给药途径递送细胞因子。然而,鉴于其临床潜力以及近期在癌症免疫治疗中的临床成功,细胞因子在临床前和临床研究中仍被广泛探索,一系列分子和制剂工程策略正在被应用,以降低治疗毒性,同时维持或提高治疗效果。本综述简要介绍了细胞因子的特性及其作为临床治疗药物的历史,随后深入讨论了为细胞因子治疗开发的工程策略,重点关注这些方法的转化相关性。

相似文献

1
Engineering Strategies for Immunomodulatory Cytokine Therapies - Challenges and Clinical Progress.
Adv Ther (Weinh). 2021 Aug;4(8). doi: 10.1002/adtp.202100035. Epub 2021 Apr 2.
2
Engineering cytokines for cancer immunotherapy: a systematic review.
Front Immunol. 2023 Jul 6;14:1218082. doi: 10.3389/fimmu.2023.1218082. eCollection 2023.
3
Engineering interferons and interleukins for cancer immunotherapy.
Adv Drug Deliv Rev. 2022 Mar;182:114112. doi: 10.1016/j.addr.2022.114112. Epub 2022 Jan 24.
4
Spatiotemporally programming cytokine immunotherapies through protein engineering.
Immunol Rev. 2023 Nov;320(1):10-28. doi: 10.1111/imr.13234. Epub 2023 Jul 6.
5
Advances in engineering and delivery strategies for cytokine immunotherapy.
Expert Opin Drug Deliv. 2023 May;20(5):579-595. doi: 10.1080/17425247.2023.2208344. Epub 2023 May 3.
6
Revitalizing Cytokine-Based Cancer Immunotherapy through Advanced Delivery Systems.
Macromol Biosci. 2023 Dec;23(12):e2300275. doi: 10.1002/mabi.202300275. Epub 2023 Aug 29.
7
Cytokine engineering for targeted cancer immunotherapy.
Curr Opin Chem Biol. 2021 Jun;62:43-52. doi: 10.1016/j.cbpa.2021.01.007. Epub 2021 Mar 6.
8
Cytokine sustained delivery for cancer therapy; special focus on stem cell- and biomaterial- based delivery methods.
Pathol Res Pract. 2023 Jul;247:154528. doi: 10.1016/j.prp.2023.154528. Epub 2023 May 9.
9
Engineered Cytokines for Cancer and Autoimmune Disease Immunotherapy.
Adv Healthc Mater. 2021 Aug;10(15):e2002214. doi: 10.1002/adhm.202002214. Epub 2021 Mar 9.
10
Facts and Hopes: Immunocytokines for Cancer Immunotherapy.
Clin Cancer Res. 2023 Oct 2;29(19):3841-3849. doi: 10.1158/1078-0432.CCR-22-1837.

引用本文的文献

3
Development of novel neutralizing single-chain fragment variable antibodies against S100A8.
Sci Rep. 2025 Apr 12;15(1):12618. doi: 10.1038/s41598-025-96211-3.
5
Aptamer based immunotherapy: a potential solid tumor therapeutic.
Front Immunol. 2025 Feb 17;16:1536569. doi: 10.3389/fimmu.2025.1536569. eCollection 2025.
6
Cytokine-overexpressing dendritic cells for cancer immunotherapy.
Exp Mol Med. 2024 Dec;56(12):2559-2568. doi: 10.1038/s12276-024-01353-5. Epub 2024 Dec 2.
7
Splicing by Overlap Extension PCR for the Production of Fusion Proteins.
Methods Mol Biol. 2025;2853:17-31. doi: 10.1007/978-1-0716-4104-0_3.
8
Implications of glycosylation for the development of selected cytokines and their derivatives for medical use.
Biotechnol Adv. 2024 Dec;77:108467. doi: 10.1016/j.biotechadv.2024.108467. Epub 2024 Oct 22.
10
Engineering Functional Particles to Modulate T Cell Responses.
Acc Mater Res. 2024 Jul 18;5(9):1048-1058. doi: 10.1021/accountsmr.4c00105. eCollection 2024 Sep 27.

本文引用的文献

2
Cancer Cell Coating Nanoparticles for Optimal Tumor-Specific Cytokine Delivery.
ACS Nano. 2020 Sep 22;14(9):11238-11253. doi: 10.1021/acsnano.0c03109. Epub 2020 Sep 5.
4
Cellular backpacks for macrophage immunotherapy.
Sci Adv. 2020 Apr 29;6(18):eaaz6579. doi: 10.1126/sciadv.aaz6579. eCollection 2020 May.
6
Albumin fusion with granulocyte-macrophage colony-stimulating factor acts as an immunotherapy against chronic tuberculosis.
Cell Mol Immunol. 2021 Oct;18(10):2393-2401. doi: 10.1038/s41423-020-0439-2. Epub 2020 May 7.
8
Cytokine-Encapsulated Biodegradable Microspheres for Immune Therapy.
Immunol Invest. 2020 Oct;49(7):824-839. doi: 10.1080/08820139.2020.1752713. Epub 2020 Apr 22.
9
Functional and mechanistic advantage of the use of a bifunctional anti-PD-L1/IL-15 superagonist.
J Immunother Cancer. 2020 Apr;8(1). doi: 10.1136/jitc-2019-000493.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验