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用于预防同种异体移植排斥反应的微米和纳米颗粒药物递送系统。

Micro and nanoparticle drug delivery systems for preventing allotransplant rejection.

作者信息

Fisher James D, Acharya Abhinav P, Little Steven R

机构信息

Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA; School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA; The Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA, USA; The McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

The McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA, USA; Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

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.

摘要

尽管移植免疫学在过去几十年取得了进展,但急性同种异体移植排斥反应所导致的组织损伤仍是移植受者发病和死亡的主要原因。此外,终身免疫抑制的长期后遗症使患者有患一系列其他有害病症的风险。使用微米和纳米颗粒(MNPs)进行可控药物递送是一种有效的方法,可将给定药物的更高局部剂量递送至特定组织和细胞,同时减轻全身效应。在此,我们综述了几种旨在延长同种异体移植存活时间的MNP免疫疗法的描述。我们还讨论了仿生药物递送领域的进展,该领域利用MNP构建体诱导和募集我们自身的抑制性免疫细胞。最后,我们对与这些药物递送系统相关的监管途径发表评论。总体而言,我们希望本综述中描述的研究将有助于开创器官移植免疫治疗的新时代。

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