Micro and nanoparticle drug delivery systems for preventing allotransplant rejection

Clin Immunol. 2015 Sep;160(1):24-35. doi: 10.1016/j.clim.2015.04.013. Epub 2015 May 1.

Abstract

Despite decades of advances in transplant immunology, tissue damage caused by acute allograft rejection remains the primary cause of morbidity and mortality in the transplant recipient. Moreover, the long-term sequelae of lifelong immunosuppression leaves patients at risk for developing a host of other deleterious conditions. Controlled drug delivery using micro- and nanoparticles (MNPs) is an effective way to deliver higher local doses of a given drug to specific tissues and cells while mitigating systemic effects. Herein, we review several descriptions of MNP immunotherapies aimed at prolonging allograft survival. We also discuss developments in the field of biomimetic drug delivery that use MNP constructs to induce and recruit our bodies' own suppressive immune cells. Finally, we comment on the regulatory pathway associated with these drug delivery systems. Collectively, it is our hope the studies described in this review will help to usher in a new era of immunotherapy in organ transplantation.

Keywords: Biomaterials; Biomimetic; Controlled release; Microparticles; Nanoparticles; Transplant immunology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antigen-Presenting Cells / immunology
  • Antimetabolites / therapeutic use
  • Drug Delivery Systems / methods*
  • Graft Rejection / immunology
  • Graft Rejection / prevention & control*
  • Graft Survival / drug effects*
  • Graft Survival / immunology
  • Humans
  • Immunosuppression Therapy / methods
  • Immunosuppressive Agents / therapeutic use*
  • Immunotherapy / methods
  • Nanoparticles / therapeutic use*
  • T-Lymphocytes, Regulatory / immunology
  • Transplantation Tolerance / immunology

Substances

  • Antimetabolites
  • Immunosuppressive Agents