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Cha, Chaenyung
Integrative Biomaterials Engineering Lab.
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Microfluidics-assisted fabrication of natural killer cell-laden microgel enhances the therapeutic efficacy for tumor immunotherapy

Author(s)
Lee, DongjinKim, Seok MinKim, DahongBaek, Seung YeopYeo, Seon JuLee, Jae JongCha, ChaenyungPark, Su A.Kim, Tae-Don
Issued Date
2024-06
DOI
10.1016/j.mtbio.2024.101055
URI
https://scholarworks.unist.ac.kr/handle/201301/82993
Citation
MATERIALS TODAY BIO, v.26, pp.101055
Abstract
Recently, interest in cancer immunotherapy has increased over traditional anti-cancer therapies such as chemotherapy or targeted therapy. Natural killer (NK) cells are part of the immune cell family and essential to tumor immunotherapy as they detect and kill cancer cells. However, the disadvantage of NK cells is that cell culture is difficult. In this study, porous microgels have been fabricated using microfluidic channels to effectively culture NK cells. Microgel fabrication using microfluidics can be mass-produced in a short time and can be made in a uniform size. Microgels consist of photo cross-linkable polymers such as methacrylic gelatin (GelMa) and can be regulated via controlled GelMa concentrations. NK92 cell-laden three-dimensional (3D) microgels increase mRNA expression levels, NK92 cell proliferation, cytokine release, and anti-tumor efficacy, compared with twodimensional (2D) cultures. In addition, the study confirms that 3D-cultured NK92 cells enhance anti-tumor effects compared with enhancement by 2D-cultured NK92 cells in the K562 leukemia mouse model. Microgels containing healthy NK cells are designed to completely degrade after 5 days allowing NK cells to be released to achieve cell-to-cell interaction with cancer cells. Overall, this microgel system provides a new cell culture platform for the effective culturing of NK cells and a new strategy for developing immune cell therapy.
Publisher
ELSEVIER
ISSN
2590-0064
Keyword (Author)
Microgel mechanicsMicrogel degradationCancer immunotherapyDouble flow -focusing microfluidicsNK92 cell encapsulation
Keyword
GELATINHYDROGELCULTURENKMICROSPHERESACTIVATIONMECHANISMS

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