Nanoparticles for generating antigen-specific T cells for immunotherapy

Savannah E. Est-Witte, Natalie K. Livingston, Mary O. Omotoso, Jordan J. Green, Jonathan P. Schneck

Research output: Contribution to journalReview articlepeer-review

Abstract

T cell therapy shows promise as an immunotherapy in both immunostimulatory and immunosuppressive applications. However, the forms of T cell-based therapy that are currently in the clinic, such as adoptive cell transfer and vaccines, are limited by cost, time-to-treatment, and patient variability. Nanoparticles offer a modular, universal platform to improve the efficacy of various T cell therapies as nanoparticle properties can be easily modified for enhanced cell targeting, organ targeting, and cell internalization. Nanoparticles can enhance or even replace endogenous cells during each step of generating an antigen-specific T cell response – from antigen presentation and T cell activation to T cell maintenance. In this review, we discuss the unique applications of nanoparticles for antigen-specific T cell therapy, focusing on nanoparticles as vaccines (to activate endogenous antigen presenting cells (APCs)), as artificial Antigen Presenting Cells (aAPCs, to directly activate T cells), and as drug delivery vehicles (to support activated T cells).

Original languageEnglish (US)
Article number101541
JournalSeminars in immunology
Volume56
DOIs
StatePublished - Aug 2021

Keywords

  • Bioengineering
  • Cell therapy
  • Immunoengineering
  • Immunotherapy
  • Nanoparticle
  • T cell

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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