Comins-Boo Alejandra, Mora-Fernández Víctor Manuel, Padrón-Aunceame Paula, Toriello-Suárez María, González-López Elena, Roa-Bautista Adriel, Castro-Hernández Carolina, Iturbe-Fernández David, Cifrián José Manuel, López-Hoyos Marco, San Segundo David
Immunology Department, Immunopathology Group, Marqués de Valdecilla University Hospital-IDIVAL, Santander, Spain.
Neumology Department, Immunopathology Group, Marqués de Valdecilla University Hospital-IDIVAL, Santander, Spain.
Transplant Proc. 2025 Jan-Feb;57(1):73-76. doi: 10.1016/j.transproceed.2024.11.031. Epub 2025 Jan 2.
Antibody-mediated rejection (ABMR) has become one of the leading causes of chronic lung graft dysfunction. However, in lung transplantation, this entity is sometimes difficult and controversial to diagnose. It is mainly caused by the appearance of donor-specific anti-human leukocyte antigen (HLA) antibodies (DSA), although there are situations with C4d deposits in biopsy in the absence of circulating DSA. The aim of this work was to study the potential role of non-HLA antibodies in the development of ABMR without DSA after lung transplantation.
A case-control study was designed with a cohort of lung transplant recipients at our institution. Twenty-seven patients with ABMR and without anti-HLA antibodies were identified after lung transplantation, and a control group of 21 transplant recipients was selected with the same post-transplant follow-up without evidence of rejection. Non-HLA antibodies were studied pretransplant using Luminex (ThermoFisher, One Lambda).
The median of the pretransplant non-HLA-positive antibodies in the group with ABMR without DSA is significantly higher than in the control group: 2 (interquartile range, 0-16) vs 0 (interquartile range, 0-1; P < .01). Patients with >1.5 pretransplant non-HLA antibodies were more likely to develop ABMR without DSA (sensitivity, 80.95%; specificity, 55.55%; area under the curve, 71.3%).
The increase of non-HLA antibodies before lung transplantation has recently been shown to increase the risk of chronic lung allograft dysfunction. These results confirm that patients with a higher number of non-HLA antibodies could be at risk of developing ABMR without DSA. These results point out the possible usefulness of pre-lung transplant non-HLA antibodies to identify patients with end-stage lung disease at risk of developing ABMR without DSA.
抗体介导的排斥反应(ABMR)已成为慢性肺移植功能障碍的主要原因之一。然而,在肺移植中,这种情况有时诊断困难且存在争议。它主要由供体特异性抗人白细胞抗原(HLA)抗体(DSA)的出现引起,尽管在活检中有C4d沉积但无循环DSA的情况也存在。这项研究的目的是探讨非HLA抗体在肺移植后无DSA的ABMR发生中的潜在作用。
在我们机构对一组肺移植受者进行病例对照研究。肺移植后确定了27例有ABMR且无抗HLA抗体的患者,并选择了21例移植受者作为对照组,其移植后随访情况相同且无排斥反应证据。移植前使用Luminex(赛默飞世尔科技,One Lambda)检测非HLA抗体。
无DSA的ABMR组移植前非HLA阳性抗体的中位数显著高于对照组:2(四分位间距,0 - 16)对0(四分位间距,0 - 1;P <.01)。移植前非HLA抗体>1.5的患者更有可能发生无DSA的ABMR(敏感性,80.95%;特异性,55.55%;曲线下面积,71.3%)。
最近研究表明肺移植前非HLA抗体增加会增加慢性肺移植功能障碍的风险。这些结果证实非HLA抗体数量较多的患者可能有发生无DSA的ABMR的风险。这些结果指出肺移植前非HLA抗体对于识别有发生无DSA的ABMR风险的终末期肺病患者可能有用。