Diagnosis and treatment of acute graft-versus-host disease after liver transplantation: Report of six cases

被引:3
|
作者
Tian, Min [1 ]
Lyu, Yi [1 ]
Wang, Bo [1 ]
Liu, Chang [1 ]
Yu, Liang [1 ]
Shi, Jian-Hua [1 ]
Liu, Xue-Min [1 ]
Zhang, Xiao-Gang [1 ]
Guo, Kun [1 ]
Li, Yu [1 ]
Hu, Liang-Shuo [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Hepatobiliary Surg, Affiliated Hosp 1, 277 West Yanta Rd, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Graft-versus-host disease; Liver transplantation; Donor T-lymphocytes chimerism; Gut microbiota; Donor-targeted serotherapy; Case report; MICROBIOTA; CHIMERISM; THERAPY; BLOOD; RISK;
D O I
10.12998/wjcc.v9.i30.9255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND 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. CASE SUMMARY Between January 1(st), 2000 and December 31(st), 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. CONCLUSION 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.
引用
收藏
页码:9255 / 9268
页数:14
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