Baudry Guillaume, Pozzi Matteo, Aubry Matthieu, Hugon-Vallet Elisabeth, Mocan Raluca, Chalabreysse Lara, Portran Philippe, Obadia Jean-François, Thaunat Olivier, Girerd Nicolas, Dubois Valérie, Sebbag Laurent
Heart Failure and Transplant Department, Hospices Civils de Lyon, Louis Pradel Hospital, 69500 Bron, France.
Centre d'Investigations Cliniques Plurithématique 1433, Université de Lorraine, INSERM DCAC, CHRU de Nancy, F-CRIN INI-CRCT, 54500 Vandœuvre-lès-Nancy, France.
J Clin Med. 2022 Jun 28;11(13):3731. doi: 10.3390/jcm11133731.
Introduction: De novo anti-HLA donor specific antibodies (DSA) have been inconsistently associated with cardiac allograft vasculopathy (CAV) and long-term mortality. We tested whether C3d-binding de novo DSA were associated with CAV or long-term-survival. Methods: We included 282 consecutive patients without preformed DSA on coronary angiography between 2010 and 2012. Angiographies were classified according to CAV ISHLT grading. The primary outcome was a composite criterion of severe CAV or mortality. As the impact of de novo antibodies should be assessed only after appearance, we used a Cox regression with time-dependent covariables. Results: Of the 282 patients, 51(18%) developed de novo DSA during follow-up, 29 patients had DSA with C3d-binding ability (DSA+C3d+), and 22 were without C3d-binding ability (DSA+C3d-). Compared with patients without DSA, DSA+C3d+ patients had an increased risk for the primary outcome of severe CAV or mortality (adjusted HR = 4.31 (2.40−7.74) p < 0.001) and long-term mortality (adjusted HR = 3.48 (1.97−6.15) p < 0.001) whereas DSA+C3d- did not (adjusted HR = 1.04 (0.43−2.47) p = 0.937 for primary outcome and HR = 1.08 (0.45−2.61) p = 0.866 for mortality). Conclusion: According to this large monocentric study in heart transplant patients, donor specific antibodies were associated with worse clinical outcome when binding complement. DSA and their complement-binding ability should thus be screened for to optimize heart transplant patient follow-up.
新生供者特异性抗人白细胞抗原抗体(DSA)与心脏移植血管病变(CAV)及长期死亡率之间的关联并不一致。我们测试了结合C3d的新生DSA是否与CAV或长期生存相关。方法:我们纳入了2010年至2012年间282例冠状动脉造影时无预先形成DSA的连续患者。血管造影根据CAV国际心脏和肺移植学会(ISHLT)分级进行分类。主要结局是严重CAV或死亡的复合标准。由于新生抗体的影响应仅在出现后进行评估,我们使用了具有时间依赖性协变量的Cox回归。结果:在282例患者中,51例(18%)在随访期间出现新生DSA,29例患者的DSA具有C3d结合能力(DSA+C3d+),22例无C3d结合能力(DSA+C3d-)。与无DSA的患者相比,DSA+C3d+患者发生严重CAV或死亡这一主要结局的风险增加(校正风险比[HR]=4.31[2.40-7.74],p<0.001),长期死亡率也增加(校正HR=3.48[1.97-6.15],p<0.001),而DSA+C3d-患者则不然(主要结局校正HR=1.04[0.43-2.47],p=0.937;死亡率校正HR=1.08[0.45-2.61],p=0.866)。结论:根据这项针对心脏移植患者的大型单中心研究,供者特异性抗体在结合补体时与更差的临床结局相关。因此,应筛查DSA及其补体结合能力,以优化心脏移植患者的随访。