Coating biomimetic nanoparticles with chimeric antigen receptor T cell-membrane provides high specificity for hepatocellular carcinoma photothermal therapy treatment

Theranostics. 2020 Jan 1;10(3):1281-1295. doi: 10.7150/thno.40291. eCollection 2020.

Abstract

Rationale: Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies in the world. Apart from traditional surgical resection, radiotherapy, and chemotherapy, more recent techniques such as nano-photothermal therapy and biotherapy are gradually being adopted for the treatment of HCC. This project intends to combine the advantages of nanoscale drug delivery systems with the targeting ability of CAR-T cells. Method: Based on cell membrane-coated nanoparticles and cell membrane-targeting modifications, a novel nanomaterial was prepared by coating CAR-T cell membranes specifically recognizing GPC3+ HCC cells onto mesoporous silica containing IR780 nanoparticles. Subsequently, the physical properties were characterized, and the in vitro and in vivo targeting abilities of this nanoparticle were verified. Results: CAR-T cells were constructed which could recognize GPC3 expressed on the cell surface of HCC cells. Then the isolated CAR-T cell membrane was successfully coated on the IR780 loaded mesoporous silica materials, as verified by transmission electron microscopy. The superior targeting ability of CAR-T cell membrane coated nanoparticles compared to IR780 loaded mesoporous silica nanoparticles was verified, both in vitro and in vivo. Conclusion: This new nanomaterial exhibits photothermal antitumor abilities along with enhanced targeting abilities, suggesting a promising strategy for the treatment of HCC.

Keywords: Nanoparticles; cell membrane coating technique; chimeric antigen receptor T cell; hepatocellular carcinoma.; photothermal therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Biomimetic Materials / chemistry
  • Carcinoma, Hepatocellular / drug therapy*
  • Cell Line, Tumor
  • Drug Carriers / chemistry
  • Glypicans / metabolism*
  • Humans
  • Immunotherapy, Adoptive*
  • Liver Neoplasms, Experimental / drug therapy
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Nanoparticles / chemistry*
  • Photothermal Therapy*
  • Receptors, Chimeric Antigen / therapeutic use*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / pathology

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • GPC3 protein, human
  • Glypicans
  • Receptors, Chimeric Antigen