Division of Hematology, University Hospital Basel, Basel, Switzerland.
Int J Lab Hematol. 2020 Apr;42(2):145-151. doi: 10.1111/ijlh.13130. Epub 2019 Nov 26.
Early detection of endothelial graft-vs-host disease (GVHD) after hematopoietic stem cell transplantation (HSCT) might help protect the patient from the late and severe complications of transplant-associated thrombotic microangiopathy (TA-TMA). Appearance of schistocytes in peripheral blood is one of the cardinal diagnostic features of TA-TMA. Our aim was to test the diagnostic accuracy and objectiveness of digital microscopy with respect to the recognition and quantification of schistocytes in the setting of endothelial GVHD.
Peripheral blood smears from 127 allogeneic and 63 autologous HSCT patients (January 2016-June 2017) were retrospectively examined before, 1 month and at 2-3 months after transplantation using digital microscopy. Peripheral blood smears from 31 healthy blood donors were also analyzed as the control group.
Assessment by digital microscopy showed that schistocytes are significantly increased after 3 months from the allogeneic (P < .001) or the autologous HSCT (P < .001) compared to the control group. Significantly higher schistocyte counts were found in patients with acute GVHD (P = .05) and in patients with HLA mismatch (P = .005). Patients in the upper quartile of the schistocyte counts had significantly more frequently acute GVHD (P = .024) or HLA mismatch (P = .035).
Schistocytes can be reliably counted by means of a digital microscopy system and are significantly higher in patients with acute GVHD and HLA mismatch. Inversely, patients with the highest numbers of schistocytes are more frequently affected by aGVHD, implying that high schistocyte counts after HSCT might be a surrogate marker for this complication.
造血干细胞移植(HSCT)后早期发现内皮细胞移植物抗宿主病(GVHD)可能有助于保护患者免受移植相关血栓性微血管病(TA-TMA)的晚期和严重并发症的影响。外周血中出现裂体细胞是 TA-TMA 的主要诊断特征之一。我们的目的是测试数字显微镜在识别和量化内皮细胞 GVHD 中的裂体细胞方面的诊断准确性和客观性。
回顾性分析了 2016 年 1 月至 2017 年 6 月期间 127 例异基因和 63 例自体 HSCT 患者移植前、移植后 1 个月和 2-3 个月的外周血涂片,采用数字显微镜进行检查。还分析了 31 例健康献血者的外周血涂片作为对照组。
数字显微镜评估显示,与对照组相比,异基因(P<.001)或自体 HSCT(P<.001)后 3 个月裂体细胞明显增加。急性 GVHD 患者(P=.05)和 HLA 错配患者(P=.005)的裂体细胞计数明显更高。裂体细胞计数处于上四分位数的患者更频繁地发生急性 GVHD(P=.024)或 HLA 错配(P=.035)。
数字显微镜系统可以可靠地计数裂体细胞,并且在急性 GVHD 和 HLA 错配患者中明显更高。相反,裂体细胞计数最高的患者更频繁地受到 aGVHD 的影响,这意味着 HSCT 后高裂体细胞计数可能是这种并发症的替代标志物。