TY - JOUR
T1 - The Effect of the Nanoparticle Shape on T Cell Activation
AU - Oh, Jiwon
AU - Xia, Xingyu
AU - Wong, Wai Ki Ricky
AU - Wong, Siu Hong Dexter
AU - Yuan, Weihao
AU - Wang, Haixing
AU - Lai, Chun Him Nathanael
AU - Tian, Ye
AU - Ho, Yi Ping
AU - Zhang, Honglu
AU - Zhang, Yuan
AU - Li, Gang
AU - Lin, Yuan
AU - Bian, Liming
N1 - Funding Information:
J.O. and X.X. contributed equally to this work. This work was supported by the Research Grants Council of the Hong Kong Special Administration Region (project no. GRF/17257016, GRF/17210618) and the National Natural Science Foundation of China (project no. 11872325). This work was supported by General Research Fund Grants from the Research Grants Council of Hong Kong (project no. 14202920 and 14204618) and partially supported by Hong Kong Research Grants Council Theme‐based Research Scheme (Ref. T13‐402/17‐N). The authors appreciate the unlimited support of samples preparation, TEM and SEM imaging guidance by the technicians: Josie Lai, Samuel Wong, Crol Yan and Anny Cheung from microscopy and imaging core of School of Biomedical Sciences, The Chinese University of Hong Kong.
Funding Information:
J.O. and X.X. contributed equally to this work. This work was supported by the Research Grants Council of the Hong Kong Special Administration Region (project no. GRF/17257016, GRF/17210618) and the National Natural Science Foundation of China (project no. 11872325). This work was supported by General Research Fund Grants from the Research Grants Council of Hong Kong (project no. 14202920 and 14204618) and partially supported by Hong Kong Research Grants Council Theme-based Research Scheme (Ref. T13-402/17-N). The authors appreciate the unlimited support of samples preparation, TEM and SEM imaging guidance by the technicians: Josie Lai, Samuel Wong, Crol Yan and Anny Cheung from microscopy and imaging core of School of Biomedical Sciences, The Chinese University of Hong Kong.
Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/9/8
Y1 - 2022/9/8
N2 - The 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.
AB - The 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.
KW - anisotropic nanomaterials
KW - cell membrane tension
KW - nanoscale ligand presentation
KW - T cell activation
UR - https://www.scopus.com/pages/publications/85126300921
U2 - 10.1002/smll.202107373
DO - 10.1002/smll.202107373
M3 - Journal article
C2 - 35297179
AN - SCOPUS:85126300921
SN - 1613-6810
VL - 18
JO - Small
JF - Small
IS - 36
M1 - 2107373
ER -