Tian Min, Lyu Yi, Wang Bo, Liu Chang, Yu Liang, Shi Jian-Hua, Liu Xue-Min, Zhang Xiao-Gang, Guo Kun, Li Yu, Hu Liang-Shuo
Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, Shaanxi Province, China.
World J Clin Cases. 2021 Oct 26;9(30):9255-9268. doi: 10.12998/wjcc.v9.i30.9255.
Graft-versus-host disease (GVHD) following liver transplantation (LT) is an unpredictable complication with poor outcome. However, consensus regarding the diagnosis and therapeutic regimen for the disease is yet lacking. The present study summarized the clinical experience on the diagnosis and treatment of acute GVHD (aGVHD) following LT and reviewed the pertinent literature.
Between January 1, 2000 and December 31, 2020, a total of 1053 LT were performed in the First Affiliated Hospital of Xi'an Jiaotong University. Six recipients developed aGVHD with clinical symptoms of fever, rash, diarrhea, and pancytopenia. The incidence of aGVHD was 0.57%. The median time from LT to the clinical presentation of aGVHD was 22.17 d. The median time from the beginning of the clinical symptom to histopathological diagnosis was 7.5 d. All six cases underwent treatment of immunosuppressant adjustment, corticosteroids, human normal immunoglobulin, and antithymocyte globulin/IL-2 antagonists. Despite intensive treatment strategies, 4 patients were deceased due to sepsis, multiple organ failure, and cerebral hemorrhage. The remaining two cases were discharged as treatment successfully. However, one died because of tuberculosis infection on the 6th month of follow-up, the other one was alive healthy during 30 mo of follow-up.
The rapid diagnosis of aGVHD is mainly based on the time from the first symptom, histopathological features, and the donor T-lymphocyte chimerism. Our cases report highlights massive corticosteroid therapy and age difference between donors and recipients could accelerate to aGVHD. Moreover, gut microbial interventions and donor-targeted serotherapy may provide novel therapeutics.
肝移植(LT)后移植物抗宿主病(GVHD)是一种预后不良的不可预测的并发症。然而,关于该疾病的诊断和治疗方案仍缺乏共识。本研究总结了肝移植后急性GVHD(aGVHD)的诊断和治疗临床经验,并复习了相关文献。
2000年1月1日至2020年12月31日,西安交通大学第一附属医院共进行了1053例肝移植手术。6例受者发生了aGVHD,出现发热、皮疹、腹泻和全血细胞减少等临床症状。aGVHD的发生率为0.57%。从肝移植到aGVHD临床表现的中位时间为22.17天。从临床症状出现到组织病理学诊断的中位时间为7.5天。所有6例均接受了免疫抑制剂调整、糖皮质激素、人正常免疫球蛋白和抗胸腺细胞球蛋白/白细胞介素-2拮抗剂治疗。尽管采取了强化治疗策略,4例患者因败血症、多器官功能衰竭和脑出血死亡。其余2例治疗成功出院。然而,其中1例在随访第6个月因结核感染死亡,另1例在30个月的随访期间健康存活。
aGVHD的快速诊断主要基于首发症状出现的时间、组织病理学特征和供体T淋巴细胞嵌合现象。我们的病例报告强调,大剂量糖皮质激素治疗以及供受者之间的年龄差异可能加速aGVHD的发生。此外,肠道微生物干预和针对供体的血清疗法可能提供新的治疗方法。