Timofte-Zorila Mihaela-Madalina, Pavel-Tanasa Mariana, Constantinescu Daniela, Cianga Corina, Branisteanu Daniel Constantin, Giannaccare Giuseppe, Lixi Filippo, Dascalescu Angela, Vlas Nicoleta, Turcas Sabina, Preda Cristina
Faculty of Medicine, Grigore T. Popa University of Medicine and Pharmacy, 700115 Iasi, Romania.
Department of Ophthalmology, Cai Ferate Clinical Hospital, 700506 Iasi, Romania.
Int J Mol Sci. 2025 May 1;26(9):4311. doi: 10.3390/ijms26094311.
Ocular graft versus host disease (oGVHD) is a common complication of allogeneic hematopoietic stem cell transplantation and may be associated with dry eye disease and chronic inflammation and fibrosis. Immune dysregulation, particularly the Th1/Th2 imbalance, plays a key role in the progression of oGVHD. This case study presents two oGVHD patients (a 20-year-old with acute oGVHD and a 59-year-old with chronic oGVHD), analyzing clinical dry eye parameters (Schirmer test I, tear film break-up time, Ocular Surface Disease Index (OSDI), and kerato-conjunctival staining) alongside tear biomarkers. A 27-plex tear cytokine analysis was performed using the Luminex200 platform, assessing various biomarkers against a control group-defined normal range. Key biomarkers included beta2-microglobulin (β2-MG), complement components, chemokines, growth factors, and both pro-inflammatory and anti-inflammatory cytokines, as well a series of soluble ligand and receptors. The study identified distinct biomarker progression patterns during topical corticosteroid treatment in the acute oGHVD patient, suggesting potential shifts in Th1/Th2 responses as the disease progressed. Notably, the soluble CD27, TNF-related apoptosis-inducing ligand (TRAIL) receptor 2 (TRAIL-R2), chemokine ligand 2 (CCL2), and IL-1β, initially elevated, normalized during treatment, while tear-soluble Fas remained highly elevated (>400-fold). Conversely, soluble TRAIL, which was initially at very low levels (100-fold lower), increased during treatment and reached normal tear levels, coinciding with improvements in the clinical ocular inflammation symptoms and OSDI score. This case study also highlights potential differences between acute and chronic oGVHD, particularly in the distinct patterns of novel tear biomarkers such as CD27, TRAIL/TRAIL-R2, and CCL2. Enhancing our understanding of biomarker dynamics may improve disease monitoring and pave the way for personalized management strategies to improve patient outcomes.
眼部移植物抗宿主病(oGVHD)是异基因造血干细胞移植的常见并发症,可能与干眼症、慢性炎症和纤维化有关。免疫失调,尤其是Th1/Th2失衡,在oGVHD的进展中起关键作用。本病例研究介绍了两名oGVHD患者(一名20岁的急性oGVHD患者和一名59岁的慢性oGVHD患者),分析了临床干眼参数(Schirmer试验I、泪膜破裂时间、眼表疾病指数(OSDI)和角膜结膜染色)以及泪液生物标志物。使用Luminex200平台进行了27种泪液细胞因子分析,根据对照组定义的正常范围评估各种生物标志物。关键生物标志物包括β2-微球蛋白(β2-MG)、补体成分、趋化因子、生长因子、促炎和抗炎细胞因子,以及一系列可溶性配体和受体。该研究确定了急性oGHVD患者局部使用皮质类固醇治疗期间不同的生物标志物进展模式,表明随着疾病进展Th1/Th2反应可能发生变化。值得注意的是,可溶性CD27、肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体2(TRAIL-R2)、趋化因子配体2(CCL2)和IL-1β最初升高,在治疗期间恢复正常,而泪液可溶性Fas仍高度升高(>400倍)。相反,最初水平极低(低100倍)的可溶性TRAIL在治疗期间增加并达到正常泪液水平,这与临床眼部炎症症状和OSDI评分的改善相一致。本病例研究还突出了急性和慢性oGVHD之间的潜在差异,特别是在CD27、TRAIL/TRAIL-R2和CCL2等新型泪液生物标志物的不同模式方面。加强对生物标志物动态变化的理解可能有助于改善疾病监测,并为改善患者预后的个性化管理策略铺平道路。