Kupis Alexander, Buchtele Nina, Wohlfarth Philipp, Rabitsch Werner, Kovacevic Miljevic Katarina D, Mussbacher Marion, Jilma Bernd, Schoergenhofer Christian
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Department of Internal Medicine I, Intensive Care Unit 13i2, Medical University of Vienna, Vienna, Austria.
Front Med (Lausanne). 2025 Jun 5;12:1580452. doi: 10.3389/fmed.2025.1580452. eCollection 2025.
MHC class I chain-related protein A (MICA) acts as a marker of cellular stress and its expression is a destruction-signal for NKG2D-expressing cytotoxic cells. Soluble MICA (sMICA) concentrations after allogeneic hematopoietic stem cell transplantation (HSCT) were associated with worse outcomes and graft-versus-host disease (GVHD). We hypothesized that (i) sMICA could be a prognostic biomarker for the development of GVHD and (ii) may act as an acute phase reactant.
In this prospective study we included 48 patients undergoing HSCT and drew blood samples before conditioning (baseline), during engraftment and 100 days after HSCT. The follow-up period was 1 year for each patient. Soluble MICA and established acute phase reactants (C-reactive Protein, von Willebrand Factor) were measured by enzyme-linked immunoassay (ELISA).
Of the 44 patients in the final analysis, 30 (68%) developed GVHD (16 acute GVHD, 8 chronic GVHD, 6 acute and chronic GVHD). Soluble MICA concentrations at baseline and during engraftment were significantly higher in patients who developed acute or chronic GVHD ( = 0.017). Receiver operating characteristic (ROC) curve analysis for the baseline values showed an area under the curve of 0.78 ( < 0.001; 95% confidence intervals 0.64-0.91) for diagnosis of acute or chronic GVHD. Soluble MICA concentrations above 93.5 pg/mL had a specificity of 93% for the diagnosis of GVHD, while the sensitivity was only 47%.
Soluble MICA did not correlate with other acute phase reactants and remained stable during engraftment. Soluble MICA may potentially serve as a biomarker with high specificity for the prediction of GVHD.
MHC I类链相关蛋白A(MICA)作为细胞应激的标志物,其表达是表达NKG2D的细胞毒性细胞的破坏信号。异基因造血干细胞移植(HSCT)后可溶性MICA(sMICA)浓度与较差的预后及移植物抗宿主病(GVHD)相关。我们假设:(i)sMICA可能是GVHD发生的预后生物标志物;(ii)可能作为一种急性期反应物。
在这项前瞻性研究中,我们纳入了48例接受HSCT的患者,并在预处理前(基线)、植入期及HSCT后100天采集血样。每位患者的随访期为1年。采用酶联免疫吸附测定(ELISA)法检测可溶性MICA及已确定的急性期反应物(C反应蛋白、血管性血友病因子)。
最终分析的44例患者中,30例(68%)发生了GVHD(16例急性GVHD,8例慢性GVHD,6例急性和慢性GVHD)。发生急性或慢性GVHD的患者在基线和植入期的可溶性MICA浓度显著更高(P = 0.017)。对基线值进行的受试者工作特征(ROC)曲线分析显示,诊断急性或慢性GVHD的曲线下面积为0.78(P < 0.001;95%置信区间0.64 - 0.91)。可溶性MICA浓度高于93.5 pg/mL时,诊断GVHD的特异性为93%,而敏感性仅为47%。
可溶性MICA与其他急性期反应物无关,且在植入期保持稳定。可溶性MICA可能有潜力作为预测GVHD的高特异性生物标志物。