Nanotechnology-based chimeric antigen receptor T-cell therapy in treating solid tumor

Pharmacol Res. 2022 Oct:184:106454. doi: 10.1016/j.phrs.2022.106454. Epub 2022 Sep 14.

Abstract

Chimeric Antigen Receptor (CAR) T cells have changed the therapeutic landscape of hematological malignancies with overwhelming success. The clinical success of CAR T-cell therapy in hematologic malignancies has fueled interest in exploring the technology in solid tumors. However, the treatment of solid tumors presents a unique set of challenges compared to hematological tumors. The biggest impediments to the success of CAR T cell treatment are the paucity of tumor-specific antigens that are produced selectively and uniformly and the immunosuppressive tumor microenvironment. To overcome these significant challenges, nanotechnology has been involved to improve the efficacy of CAR-T cells. In this review, we systematically introduced the components of different generations of CARs and summarized recent innovations in nano-based CAR-T cell therapy to conquer therapeutically resistant non-hematologic malignancies, including mRNA and hydrogel-based CAR T cells delivery, photothermal-remodeling, and tumor microenvironment-based CAR T cell therapy. These nanotechnologies remarkably facilitate in vivo generation of CAR T cells and hold promise as a therapeutic platform to treat solid tumors and even other diseases.

Keywords: CAR; Nanotechnology; Solid tumor; Tumor microenvironment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell- and Tissue-Based Therapy
  • Hematologic Neoplasms*
  • Humans
  • Hydrogels
  • Immunotherapy, Adoptive
  • Nanotechnology
  • Neoplasms* / pathology
  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen* / genetics
  • Tumor Microenvironment

Substances

  • Hydrogels
  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen