Elmakki Erwa Eltayib, Madkhali Mohammed Ali, Oraibi Omar, Alqassimi Sameer, Saleh Eman
Department of Internal Medicine, Faculty of Medicine, Jazan University, Jazan, SAU.
Cureus. 2023 Aug 26;15(8):e44148. doi: 10.7759/cureus.44148. eCollection 2023 Aug.
Transfusion-associated graft-versus-host disease (TA-GVHD) is a rare but fatal complication of blood transfusion that usually develops two to 30 days following a blood transfusion giving rise to graft versus host disease (GVHD) clinical features that are consisting of fever, skin rash, jaundice, diarrhea, and pancytopenia. The disease is fulminant in most patients with a mortality rate of >90% of cases. The main aim of this review is to enhance awareness among medical practitioners about this fatal disease. Data were extracted manually from the main medical databases (Medline, Scopus, and Google Scholar) after the revision of selected articles and assessed for their contribution to the knowledge of TA-GVHD. TA-GVHD occurs when the viable donor T-cells in the blood or blood products attack the recipient's tissues which his/her immune system is incapable to destroy due to several reasons. The recipient's tissues that are usually involved in TA-GVHD include the liver, intestine, skin, lungs, and bone marrow. Any blood component either whole blood, packed red blood cells (RBCs), platelets, or fresh non-frozen plasma that contains viable T lymphocytes can cause TA-GVHD. Host immunodeficiency, transfusion of fresh blood, and partial human leukocyte antigen (HLA) matching between the donors and the recipients represent the major risk factors of TA-GVHD. Partial HLA matching includes immunocompetent recipients who receive blood from a first-degree relative also, seen in genetically homogenous populations because of high rates of consanguineous marriage. The diagnosis of TA-GVHD is mainly suspected based on clinical manifestations. However, a histopathological study of either skin or rectal biopsy is diagnostic. The treatment of TA-GVHD is generally not effective, unless the patient received emergency stem cell transplantation, while prevention via irradiation of blood or blood products represents the standard of care for this disease. In conclusion, medical practitioners should have a high index of suspicion for this disease. Moreover, future clinical trials targeting and comparing the outcomes of the different therapeutic options for TA-GVHD are required.
输血相关移植物抗宿主病(TA-GVHD)是一种罕见但致命的输血并发症,通常在输血后2至30天内发生,会出现移植物抗宿主病(GVHD)的临床特征,包括发热、皮疹、黄疸、腹泻和全血细胞减少。该病在大多数患者中病情凶险,死亡率超过90%。本综述的主要目的是提高医学从业者对这种致命疾病的认识。在对选定文章进行修订后,手动从主要医学数据库(Medline、Scopus和谷歌学术)中提取数据,并评估其对TA-GVHD知识的贡献。当血液或血液制品中的存活供体T细胞攻击受者组织时,就会发生TA-GVHD,由于多种原因,受者的免疫系统无法破坏这些组织。通常参与TA-GVHD的受者组织包括肝脏、肠道、皮肤、肺和骨髓。任何含有存活T淋巴细胞的血液成分,无论是全血、浓缩红细胞(RBC)、血小板还是新鲜非冷冻血浆,都可能导致TA-GVHD。宿主免疫缺陷、输注新鲜血液以及供体与受者之间的部分人类白细胞抗原(HLA)匹配是TA-GVHD的主要危险因素。部分HLA匹配包括免疫功能正常的受者接受来自一级亲属的血液,在近亲结婚率高的基因同质人群中也可见到。TA-GVHD的诊断主要基于临床表现进行怀疑。然而,皮肤或直肠活检的组织病理学研究具有诊断意义。TA-GVHD的治疗通常无效,除非患者接受紧急干细胞移植,而通过对血液或血液制品进行辐照来预防是该病的标准治疗方法。总之,医学从业者应对这种疾病保持高度怀疑。此外,需要针对TA-GVHD的不同治疗方案进行靶向和比较结果的未来临床试验。