Perfluorocarbon nanoparticle-mediated platelet inhibition promotes intratumoral infiltration of T cells and boosts immunotherapy
Author(s) -
Zaigang Zhou,
Baoli Zhang,
Wenjing Zai,
Lin Kang,
Ahu Yuan,
Yiqiao Hu,
Jinhui Wu
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1901987116
Subject(s) - infiltration (hvac) , immunotherapy , limiting , cancer research , tumor microenvironment , platelet , t cell , cell , medicine , chemistry , immune system , immunology , tumor cells , materials science , biochemistry , mechanical engineering , composite material , engineering
Significance Trafficking of T cells to tumors is critical for the success of immunotherapy. The success against solid cancers is not as effective as desired owing to limited efficacy in delivering a higher frequency of T cells to the tumor microenvironment. At this time, no useful methods are available to enhance T-cell infiltration in tumors in a short time. New methods that could enhance T-cell trafficking in tumors are urgently in need. Up to now, the role of platelets in limiting T-cell infiltration in tumors is a neglected phenomenon. In our study, for the first time, we proved that perfluorocarbon nanoparticles could promote intratumoral infiltration of T cells via platelet inhibition, resulting in enhanced anti–PD-L1 immunotherapy.
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