Department of Thoracic, Cardiac, and Vascular Surgery, University Hospital Tuebingen, Tuebingen, Germany.
PLoS One. 2013 Jul 23;8(7):e68810. doi: 10.1371/journal.pone.0068810. Print 2013.
Target specific short single-stranded DNA (ssDNA) molecules, called aptamers, are auspicious ligands for numerous in vivo applications. However, aptamers are synthetic molecules, which might be recognized by the immune cells in vivo and induce an activation of the innate immune system. Thus, immune activation potential of synthetic ssDNA oligonucleotides (ODNs) was determined using a well established closed-loop circulation model. Fresh human blood was incubated at 37°C for 2 or 4 hours with ssDNA ODNs (SB_ODN) or CpG ODN as positive control. Transcriptional changes were determined by microarray analyses. Blood samples containing SB_ODN demonstrated after 4 hours a significant regulation of 295 transcripts. Amongst others, CCL8, CXCL10, CCL7 and CXCL11 were highest regulated genes. Gene Ontology terms and KEGG pathway analyses exhibited that the differentially expressed genes belong to the transcripts that are regulated during an immune and inflammatory response, and were overrepresented in TLR signaling pathway. This study shows for the first time the potential of aptamers to activate immune system after systemic application into the human blood. Thus, we highly recommend performing of these preclinical tests with potential aptamer-based therapeutics.
靶向特定的短单链 DNA(ssDNA)分子,称为适体,是许多体内应用的理想配体。然而,适体是合成分子,可能会被体内的免疫细胞识别,并诱导先天免疫系统的激活。因此,使用成熟的闭环循环模型来确定合成 ssDNA 寡核苷酸(ODN)的免疫激活潜力。将新鲜的人血在 37°C 下孵育 2 或 4 小时,用 ssDNA ODN(SB_ODN)或 CpG ODN 作为阳性对照。通过微阵列分析确定转录变化。含有 SB_ODN 的血液样本在 4 小时后显示出 295 个转录本的显著调节。其中,CCL8、CXCL10、CCL7 和 CXCL11 是调节最明显的基因。基因本体论术语和 KEGG 途径分析表明,差异表达的基因属于在免疫和炎症反应中调节的转录本,并且在 TLR 信号通路中过表达。这项研究首次表明,适体在全身应用于人体血液后有激活免疫系统的潜力。因此,我们强烈建议对基于潜在适体的治疗药物进行这些临床前测试。