Biomaterials and Regenerative Medicine Laboratory, School of Biomedical Engineering, Science, and Health Systems, Drexel University, Philadelphia, PA, United States.
Department of Kinesiology and Nutrition and Center for Tissue Repair and Regeneration, University of Illinois, Chicago, United States.
Adv Drug Deliv Rev. 2017 Dec 1;122:74-83. doi: 10.1016/j.addr.2017.05.010. Epub 2017 May 16.
Mounting evidence suggests that therapeutic cell and drug delivery strategies designed to actively harness the regenerative potential of the inflammatory response have great potential in regenerative medicine. In particular, macrophages have emerged as a primary target because of their critical roles in regulating multiple phases of tissue repair through their unique ability to rapidly shift phenotypes. Herein, we review macrophage-based therapies, focusing on the translational potential for cell delivery of ex vivo-activated macrophages and delivery of molecules and biomaterials to modulate accumulation and phenotype of endogenous macrophages. We also review current obstacles to progress in translating basic findings to therapeutic applications, including the need for improved understanding of context-dependent macrophage functions and the myriad factors that regulate macrophage phenotype; potential species-specific differences (e.g. humans versus mice); quality control issues; and the lack of standardized procedures and nomenclature for characterizing macrophages. Looking forward, the inherent plasticity of macrophages represents a daunting challenge for harnessing these cells in regenerative medicine therapies but also great opportunity for improving patient outcomes in a variety of pathological conditions.
越来越多的证据表明,旨在积极利用炎症反应的再生潜力的治疗性细胞和药物输送策略在再生医学中有很大的潜力。特别是,巨噬细胞因其通过其快速改变表型的独特能力在调节组织修复的多个阶段中的关键作用而成为主要靶标。在此,我们综述了基于巨噬细胞的治疗方法,重点介绍了体外激活的巨噬细胞细胞递送以及递送至调节内源性巨噬细胞积累和表型的分子和生物材料的转化潜力。我们还综述了将基础发现转化为治疗应用的当前进展障碍,包括需要更好地了解依赖于上下文的巨噬细胞功能和调节巨噬细胞表型的无数因素;潜在的种间差异(例如人类与小鼠);质量控制问题;以及缺乏用于表征巨噬细胞的标准化程序和命名法。展望未来,巨噬细胞的固有可塑性代表了在再生医学治疗中利用这些细胞的艰巨挑战,但也为改善各种病理条件下的患者预后提供了巨大机会。