Oellerich Michael, Walson Philip D, Beck Julia, Schmitz Jessica, Kollmar Otto, Schütz Ekkehard
*Institute of Clinical Pharmacology, University Medicine Göttingen, Göttingen, Germany; †Chronix Biomedical GmbH, Göttingen, Germany; and ‡Department of General, Visceral and Pediatric Surgery, University Medicine Go[Combining Diaeresis]ttingen, Göttingen, Germany.
Ther Drug Monit. 2016 Apr;38 Suppl 1:S75-9. doi: 10.1097/FTD.0000000000000239.
Although short-term success after solid organ transplantation is good, long-term graft and recipient survival are both not satisfactory. Despite therapeutic drug monitoring (TDM) of immunosuppressive drugs (ISDs), both excessive and insufficient immunosuppression still do occur. There is a need for new biomarkers that, when combined with TDM, can be used to provide more effective and less toxic, personalized immunosuppression to improve long-term survival. Currently used methods are insufficient to rapidly, cost-effectively, and directly interrogate graft integrity after solid organ transplantation. However, because organ transplants are also genome transplants, measurement of graft-derived circulating cell-free DNA (GcfDNA) has shown promise as a way to improve both graft and recipient outcomes after solid organ transplantation through the early detection of severe graft injury, enabling an early intervention. A newly developed droplet digital polymerase chain reaction (ddPCR) method has advantages over expensive high-throughput sequencing methods to rapidly quantify GcfDNA percentages and absolute amounts. This procedure does not require donor DNA and therefore can be applied to any organ donor/recipient pair. The droplet digital polymerase chain reaction method allows for the early, sensitive, specific, and cost-effective direct assessment of graft integrity and can be used to define individual responses to ISDs including the minimal ISD exposures necessary to prevent rejection. This is especially important in patients undergoing ISD switches due to ISD toxicity, infections, or malignancies. Although prospective, multicenter clinical trials in liver, heart, and kidney transplantation have not been completed, early results suggest that GcfDNA can be combined with TDM to guide changes in immunosuppression to provide more effective, and less toxic treatment. Personalized immunosuppression will shift emphasis in transplantation from reaction to prevention and could improve outcome at lower health care costs.
尽管实体器官移植后的短期成功率较高,但长期移植物和受者的存活率均不尽人意。尽管对免疫抑制药物(ISDs)进行了治疗药物监测(TDM),但免疫抑制过度和不足的情况仍然会发生。需要新的生物标志物,与TDM相结合,用于提供更有效、毒性更小的个性化免疫抑制,以提高长期存活率。目前使用的方法不足以在实体器官移植后快速、经济高效且直接地检测移植物的完整性。然而,由于器官移植也是基因组移植,测量移植物来源的循环游离DNA(GcfDNA)已显示出有望通过早期检测严重的移植物损伤来改善实体器官移植后的移植物和受者结局,从而实现早期干预。一种新开发的液滴数字聚合酶链反应(ddPCR)方法相对于昂贵的高通量测序方法具有优势,能够快速定量GcfDNA百分比和绝对量。该程序不需要供体DNA,因此可应用于任何器官供体/受体对。液滴数字聚合酶链反应方法能够对移植物完整性进行早期、灵敏、特异且经济高效的直接评估,并可用于确定个体对ISDs的反应,包括预防排斥所需的最小ISD暴露量。这对于因ISD毒性、感染或恶性肿瘤而进行ISD转换的患者尤为重要。尽管尚未完成肝、心和肾移植的前瞻性多中心临床试验,但早期结果表明,GcfDNA可与TDM相结合,以指导免疫抑制的调整,提供更有效、毒性更小的治疗。个性化免疫抑制将使移植重点从反应转向预防,并可能以更低的医疗成本改善结局。