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Article: The Effect of the Nanoparticle Shape on T Cell Activation

TitleThe Effect of the Nanoparticle Shape on T Cell Activation
Authors
Keywordsanisotropic nanomaterials
cell membrane tension
nanoscale ligand presentation
T cell activation
Issue Date8-Sep-2022
PublisherWiley
Citation
Small, 2022, v. 18, n. 36 How to Cite?
AbstractThe mechanism of extracellular ligand nano-geometry in ex vivo T cell activation for immunotherapy remains elusive. Herein, the authors demonstrate large aspect ratio (AR) of gold nanorods (AuNRs) conjugated on cell culture substrate enhancing both murine and human T cell activation through the nanoscale anisotropic presentation of stimulatory ligands (anti-CD3(αCD3) and anti-CD28(αCD28) antibodies). AuNRs with large AR bearing αCD3 and αCD28 antibodies significantly promote T cell expansion and key cytokine secretion including interleukin-2 (IL-2), interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α). High membrane tension observed in large AR AuNRs regulates actin filament and focal adhesion assembly and develops maturation-related morphological features in T cells such as membrane ruffle formation, cell spreading, and large T cell receptor (TCR) cluster formation. Anisotropic stimulatory ligand presentation promotes differentiation of naïve CD8+ T cells toward the effector phenotype inducing CD137 expression upon co-culture with human cervical carcinoma. The findings suggest the importance of manipulating extracellular ligand nano-geometry in optimizing T cell behaviors to enhance therapeutic outcomes.
Persistent Identifierhttp://hdl.handle.net/10722/350097
ISSN
2023 Impact Factor: 13.0
2023 SCImago Journal Rankings: 3.348

 

DC FieldValueLanguage
dc.contributor.authorOh, Jiwon-
dc.contributor.authorXia, Xingyu-
dc.contributor.authorWong, Wai Ki Ricky-
dc.contributor.authorWong, Siu Hong Dexter-
dc.contributor.authorYuan, Weihao-
dc.contributor.authorWang, Haixing-
dc.contributor.authorLai, Chun Him Nathanael-
dc.contributor.authorTian, Ye-
dc.contributor.authorHo, Yi Ping-
dc.contributor.authorZhang, Honglu-
dc.contributor.authorZhang, Yuan-
dc.contributor.authorLi, Gang-
dc.contributor.authorLin, Yuan-
dc.contributor.authorBian, Liming-
dc.date.accessioned2024-10-21T03:55:52Z-
dc.date.available2024-10-21T03:55:52Z-
dc.date.issued2022-09-08-
dc.identifier.citationSmall, 2022, v. 18, n. 36-
dc.identifier.issn1613-6810-
dc.identifier.urihttp://hdl.handle.net/10722/350097-
dc.description.abstractThe mechanism of extracellular ligand nano-geometry in ex vivo T cell activation for immunotherapy remains elusive. Herein, the authors demonstrate large aspect ratio (AR) of gold nanorods (AuNRs) conjugated on cell culture substrate enhancing both murine and human T cell activation through the nanoscale anisotropic presentation of stimulatory ligands (anti-CD3(αCD3) and anti-CD28(αCD28) antibodies). AuNRs with large AR bearing αCD3 and αCD28 antibodies significantly promote T cell expansion and key cytokine secretion including interleukin-2 (IL-2), interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α). High membrane tension observed in large AR AuNRs regulates actin filament and focal adhesion assembly and develops maturation-related morphological features in T cells such as membrane ruffle formation, cell spreading, and large T cell receptor (TCR) cluster formation. Anisotropic stimulatory ligand presentation promotes differentiation of naïve CD8+ T cells toward the effector phenotype inducing CD137 expression upon co-culture with human cervical carcinoma. The findings suggest the importance of manipulating extracellular ligand nano-geometry in optimizing T cell behaviors to enhance therapeutic outcomes.-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofSmall-
dc.subjectanisotropic nanomaterials-
dc.subjectcell membrane tension-
dc.subjectnanoscale ligand presentation-
dc.subjectT cell activation-
dc.titleThe Effect of the Nanoparticle Shape on T Cell Activation-
dc.typeArticle-
dc.identifier.doi10.1002/smll.202107373-
dc.identifier.pmid35297179-
dc.identifier.scopuseid_2-s2.0-85126300921-
dc.identifier.volume18-
dc.identifier.issue36-
dc.identifier.eissn1613-6829-
dc.identifier.issnl1613-6810-

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