Viklicky Ondrej, Slatinska Janka, Novotny Marek, Hruba Petra
Department of Nephrology, Transplant Center.
Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Curr Opin Organ Transplant. 2021 Feb 1;26(1):91-96. doi: 10.1097/MOT.0000000000000844.
In this review, we discuss achievements in immunosuppression in kidney transplant recipients published at last 18 months.
Results of recent trials with everolimus in low-risk primary kidney transplant recipients suggest that lowTAC/EVR combination is noninferior and CMV and BKV viral infections are less frequent to standTAC/MPA. Iscalimab monoclonal antibody, which prevents CD40 to CD154 binding, has just recently entered phase II clinical studies in kidney transplantation. Eculizumab, anti-C5 monoclonal antobody was recently shown to improve outcomes in DSA+ living-donor kidney transplant recipients requiring pretransplant desensitization because of crossmatch positivity. Proximal complement C1 inhibition in patients with antibody-mediated rejection was studied in several phase I trials.
Recent knowledge creates a path towards future immunosuppression success in sensitized recipients and in those in high risk of viral infections or CNI nephrotoxicity.
在本综述中,我们讨论过去18个月发表的肾移植受者免疫抑制方面的成果。
近期对低风险初次肾移植受者使用依维莫司的试验结果表明,低剂量他克莫司/依维莫司联合方案不差于标准他克莫司/霉酚酸酯方案,且巨细胞病毒和BK病毒感染发生率更低。抑制CD40与CD154结合的iscalimab单克隆抗体最近刚进入肾移植的II期临床研究。抗C5单克隆抗体依库珠单抗最近显示可改善因交叉配型阳性而需要移植前脱敏的DSA阳性活体供肾移植受者的预后。在多项I期试验中研究了抗体介导排斥反应患者的近端补体C1抑制作用。
最新知识为致敏受者以及有病毒感染或钙调神经磷酸酶抑制剂肾毒性高风险的受者未来免疫抑制成功开辟了道路。