Nanotechnology Characterization Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research Sponsored by the National Cancer Institute, Frederick, MD 21701, USA.
Nanoscale Science Program, Department of Chemistry, University of North Carolina Charlotte, Charlotte, NC 28223, USA.
Molecules. 2023 Jun 1;28(11):4484. doi: 10.3390/molecules28114484.
Nucleic acid nanoparticles (NANPs) require a carrier to allow for their intracellular delivery to immune cells. Cytokine production, specifically type I and III interferons, allows for reliable monitoring of the carrier effect on NANP immunostimulation. Recent studies have shown that changes in the delivery platform (e.g., lipid-based carriers vs. dendrimers) can alter NANPs' immunorecognition and downstream cytokine production in various immune cell populations. Herein, we used flow cytometry and measured cytokine induction to show how compositional variations in commercially available lipofectamine carriers impact the immunostimulatory properties of NANPs with different architectural characteristics.
核酸纳米颗粒(NANP)需要载体才能将其递送至免疫细胞内。细胞因子的产生,特别是 I 型和 III 型干扰素,可可靠地监测载体对 NANP 免疫刺激的影响。最近的研究表明,递药平台的变化(例如,基于脂质的载体与树枝状聚合物)可改变不同免疫细胞群中 NANP 的免疫识别和下游细胞因子的产生。在此,我们使用流式细胞术并测量细胞因子的诱导,以显示市售脂质体载体的组成变化如何影响具有不同结构特征的 NANP 的免疫刺激特性。