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核心技术专利:CN118964589B侵权必究
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Biomaterials for in situ cell therapy.

作者信息

Wang Chang, Wang Siyu, Kang Diana D, Dong Yizhou

机构信息

Department of Oncological Sciences, Icahn Genomics Institute, Precision Immunology Institute, Tisch Cancer Institute, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Division of Pharmaceutics & Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.

出版信息

BMEmat. 2023 Sep;1(3). doi: 10.1002/bmm2.12039. Epub 2023 Jul 19.


DOI:10.1002/bmm2.12039
PMID:39574564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11581612/
Abstract

Cell therapy has revolutionized the treatment of various diseases, such as cancers, genetic disorders, and autoimmune diseases. Currently, most cell therapy products rely on ex vivo cell engineering, which requires sophisticated manufacturing processes and poses safety concerns. The implementation of in situ cell therapy holds the potential to overcome the current limitations of cell therapy and provides a broad range of applications and clinical feasibility in the future. A variety of biomaterials have been developed to improve the function and target delivery to specific cell types due to their excellent biocompatibility, tunable properties, and other functionalities, which provide a reliable method to achieve in vivo modulation of cell reprogramming. In this article, we summarize recent advances in biomaterials for in situ cell therapy including T cells, macrophages, dendritic cells, and stem cells reprogramming leveraging lipid nanoparticles, polymers, inorganic materials, and other biomaterials. Finally, we discuss the current challenges and future perspectives of biomaterials for in situ cell therapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/544215c80361/nihms-2036321-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/64cb30dd9957/nihms-2036321-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/714e1bb498c0/nihms-2036321-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/35f3db6783e6/nihms-2036321-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/df54e3171d75/nihms-2036321-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/544215c80361/nihms-2036321-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/64cb30dd9957/nihms-2036321-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/714e1bb498c0/nihms-2036321-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/35f3db6783e6/nihms-2036321-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/df54e3171d75/nihms-2036321-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0087/11581612/544215c80361/nihms-2036321-f0009.jpg

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[1]
Biomaterials for in situ cell therapy.

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本文引用的文献

[1]
Targeted modulation of immune cells and tissues using engineered biomaterials.

Nat Rev Bioeng. 2023-2

[2]
Long-term outcomes following CAR T cell therapy: what we know so far.

Nat Rev Clin Oncol. 2023-6

[3]
RNA Delivery to Hematopoietic Stem and Progenitor Cells Targeted Lipid Nanoparticles.

Nano Lett. 2023-4-12

[4]
In Situ Reprogramming of Tumor-Associated Macrophages with Internally and Externally Engineered Exosomes.

Angew Chem Int Ed Engl. 2023-3-6

[5]
Chemically engineering cells for precision medicine.

Chem Soc Rev. 2023-2-6

[6]
Overcoming on-target, off-tumour toxicity of CAR T cell therapy for solid tumours.

Nat Rev Clin Oncol. 2023-1

[7]
Injectable Immunotherapeutic Hydrogel Containing RNA-Loaded Lipid Nanoparticles Reshapes Tumor Microenvironment for Pancreatic Cancer Therapy.

Nano Lett. 2022-11-23

[8]
Nanomaterials-Mediated Co-Stimulation of Toll-Like Receptors and CD40 for Antitumor Immunity.

Adv Mater. 2022-11

[9]
Lipid nanoparticles produce chimeric antigen receptor T cells with interleukin-6 knockdown in vivo.

J Control Release. 2022-10

[10]
Stem cell-based therapy for human diseases.

Signal Transduct Target Ther. 2022-8-6

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