Capurso Noah A, Look Michael, Jeanbart Laura, Nowyhed Heba, Abraham Clara, Craft Joe, Fahmy Tarek M
Department of Biomedical Engineering, Yale University; New Haven, CT USA.
Self Nonself. 2010 Oct;1(4):335-340. doi: 10.4161/self.1.4.13946.
Retinoic acid (RA) is a small molecule capable of shunting developing T cells away from the Th17 lineage and towards the Treg phenotype, making it a potentially useful therapeutic for autoimmune and inflammatory diseases. However, therapy can be complicated by systemic toxicity and unpredictable bioavailability, making a targeted drug delivery vehicle for local therapy desirable. A promising approach is the use of nanoparticles, which have been demonstrated to increase potency and decrease toxicity of therapies in a variety of disease models including Th17 mediated diseases. Nanoparticles can also be targeted to specific cell types via surface modification, further increasing the potential specificity of this approach. We therefore constructed a nanoparticulate drug delivery platform from poly(lactic-co-glycolic acid) (PLGA) capable of encapsulating and releasing RA. Here we report the fabrication, characterization, and in vitro bioactivity of this platform. We demonstrate that RA containing PLGA nanoparticles suppress IL-17 production and ROR-γ(t) expression in T cells polarized towards the Th17 phenotype in vitro with similar potency to that of free drug. Furthermore, we show that these particles enhance TGF-β dependent Foxp3 expression and IL-10 production of T cells in vitro with similar potency to free RA. Finally, we demonstrate that T cells polarized towards the Th17 phenotype in the presence of free and nanoparticulate RA have similarly suppressed ability to induce IL-6 production by fibroblasts. Our findings demonstrate the feasibility of RA delivery via biodegradable nanoparticles and represent an exciting technology for the treatment of autoimmune and inflammatory diseases.
视黄酸(RA)是一种小分子,能够使发育中的T细胞从Th17谱系转向Treg表型,使其成为自身免疫性疾病和炎症性疾病潜在有用的治疗药物。然而,全身毒性和不可预测的生物利用度可能会使治疗变得复杂,因此需要一种用于局部治疗的靶向药物递送载体。一种有前景的方法是使用纳米颗粒,在包括Th17介导的疾病在内的多种疾病模型中,纳米颗粒已被证明可提高治疗效果并降低毒性。纳米颗粒还可以通过表面修饰靶向特定细胞类型,进一步提高这种方法的潜在特异性。因此,我们构建了一种由聚乳酸-羟基乙酸共聚物(PLGA)制成的纳米颗粒药物递送平台,该平台能够封装和释放RA。在此,我们报告该平台的制备、表征及其体外生物活性。我们证明,含有RA的PLGA纳米颗粒在体外对向Th17表型极化的T细胞中IL-17的产生和ROR-γ(t)的表达具有抑制作用,其效力与游离药物相似。此外,我们表明这些颗粒在体外对T细胞中TGF-β依赖性Foxp3表达和IL-10产生的增强作用与游离RA相似。最后,我们证明在游离RA和纳米颗粒RA存在下向Th17表型极化的T细胞诱导成纤维细胞产生IL-6 的能力受到类似抑制。我们的研究结果证明了通过可生物降解纳米颗粒递送RA的可行性,并代表了一种用于治疗自身免疫性疾病和炎症性疾病的令人兴奋的技术。