Photodynamic amplified immune checkpoint-blockade therapy of self-delivery bioregulator via epigenetic reprogramming.

Self-delivery bioregulator (C-Moc) is developed through the self-assembly of chlorine e6 (Ce6) and mocetinostat (Moc) in the presence of DSPE-PEG 2000 via intermolecular forces. Carrier free C-Moc could not only inhibit primary tumor growth and induce immunogenic cell death (ICD) by photodynamic therapy (PDT), but also enhance the immune checkpoint-blockade (ICB) therapy by epigenetic reprogramming. [Display omitted] • High drug-loading capacity and favorable stability of self-delivery bioregulator. • Positive regulation of MHC-I and PD-L1 by HDAC1 inhibition. • Epigenetic reprogramming of C-Moc reversed immunosuppressive tumor microenvironment. • Primary and distant tumor inhibition by ICB therapy and PDT-induced ICD cascade. Photodynamic therapy (PDT) and immunotherapy have unique advantages for primary and metastatic tumor treatment. However, immunosuppressive tumor microenvironment (ITM) causes low immune responses and various degrees of therapeutic resistance. In this work, a self-delivery bioregulator (C-Moc) is developed for photodynamic amplified immune checkpoint-blockade (ICB) therapy by epigenetic reprogramming. To be specific, carrier-free C-Moc is prepared by the self-assembly of chlorine e6 (Ce6) and mocetinostat (Moc) in the presence of DSPE-PEG 2000 through electrostatic and hydrophobic interactions. Of note, nanosized C-Moc has an improved stability, cellular uptake and pharmacokinetics behaviors. Intravenously injected C-Moc prefers to accumulate at tumor site and then penetrate into tumor tissues upon light irradiation. Meanwhile, the initiated PDT would kill tumor cells for primary tumor inhibition and also induce immunogenic cell death (ICD) to activate antitumor immunity. More importantly, C-Moc is able to increase the expressions of MHC-I and PD-L1 to regulate ITM by epigenetic reprogramming, which would promote the recognition of immune system to MHC-I overexpressed tumor cells and enhance the ICB therapy of α-PD-L1. This photodynamic amplified ICB therapy of C-Moc shows a great superiority over the single treatment on primary and distant tumor suppression. [ABSTRACT FROM AUTHOR]