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Inducing Ectopic T Cell Clusters Using Stromal Vascular Fraction Spheroid-Based Immunotherapy to Enhance Anti-Tumor Immunityopen access

Authors
Lee, Jae-WonPark, Bum ChulJang, Na YoonLee, SihyeonCho, Young KyuSharma, PrashantByun, Sang WonJeon, KyeongseokJeon, Yun-HuiPark, UniRo, Hyo JinPark, Hyo ReeKim, YuriLee, Dong-SupChung, SeokKim, Young KeunCho, Nam-Hyuk
Issue Date
10월-2022
Publisher
WILEY
Keywords
cancer immunotherapy; dendritic cells; immunotherapy; iron-oxide zinc oxide nanoparticles; spheroid; stromal vascular fraction; tertiary lymphoid structure
Citation
ADVANCED SCIENCE, v.9, no.28
Indexed
SCIE
SCOPUS
Journal Title
ADVANCED SCIENCE
Volume
9
Number
28
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/146584
DOI
10.1002/advs.202203842
ISSN
2198-3844
Abstract
Tertiary lymphoid structures (TLSs) provide specialized niches for immune cells, resulting in improved prognoses for patients undergoing cancer immunotherapy. Shaping TLS-like niches may improve anti-cancer immunity and overcome the current limitations of immune cell-based immunotherapy. Here, it is shown that stromal vascular fraction (SVF) from adipose tissues can enhance dendritic cell (DC)-mediated T cell immunity by inducing ectopic T lymphocyte clusters. SVF cells expanded ex vivo have phenotypes and functions similar to those of fibroblastic reticular cells in a secondary lymphoid organ, and their properties can be modulated using three-dimensional spheroid culture and coculture with DCs spiked with antigen-loaded iron oxide-zinc oxide core-shell nanoparticles. Thereby, the combination of SVF spheroids and mature DCs significantly augments T cell recruitment and retention at the injection site. This strategy elicits enhanced antigen-specific immune response and anti-tumoral immunity in mice, illustrating the potential for a novel immunotherapeutic design using SVF as a structural scaffold for TLS.
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공과대학 (신소재공학부)
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