Rai Vikrant, Dietz Nicholas Edward, Agrawal Devendra K
a Department of Clinical and Translational Science , Creighton University School of Medicine , Omaha , NE , USA.
b Department of Pathology , Creighton University School of Medicine , Omaha , NE , USA.
Expert Rev Clin Immunol. 2016;12(5):583-93. doi: 10.1586/1744666X.2016.1145056. Epub 2016 Feb 24.
Graft versus host disease (GVHD) after liver transplant, although a rare disease, has a very high mortality rate. GVHD occurs due to immunoreactions caused by donor T lymphocytes and host cell surface antigens resulting in proliferation and clonal expansion of T lymphocyte. Migration of effector cells, including macrophages, NK cells and cytotoxic T lymphocyte, to the target organs such as skin, intestine and bone marrow results in skin rashes, diarrhea and bone marrow depression. GVHD is diagnosed by clinical symptoms, histopathological findings and by the presence of chimerism. The delayed diagnosis, opportunistic infections and lack of definitive treatment of post orthotopic liver transplant (OLT)-GVHD results in sepsis and multi-organ failure leading to very low survival rates. In this review, we have focused on early diagnosis and critically discuss novel treatment modalities to decrease the incidence of GVHD.
肝移植后的移植物抗宿主病(GVHD)虽然是一种罕见疾病,但死亡率非常高。GVHD是由供体T淋巴细胞与宿主细胞表面抗原引起的免疫反应导致T淋巴细胞增殖和克隆扩增而发生的。包括巨噬细胞、自然杀伤细胞和细胞毒性T淋巴细胞在内的效应细胞迁移至皮肤、肠道和骨髓等靶器官,会导致皮疹、腹泻和骨髓抑制。GVHD通过临床症状、组织病理学检查结果以及嵌合体的存在来诊断。原位肝移植(OLT)后GVHD的诊断延迟、机会性感染以及缺乏明确的治疗方法会导致脓毒症和多器官功能衰竭,从而导致生存率极低。在本综述中,我们重点关注早期诊断,并批判性地讨论降低GVHD发病率的新型治疗方式。