Hull R J, Bray R A, Hillyer C, Swerlick R A
Department of Medicine, Emory University School of Medicine, GA 30322, USA.
J Am Acad Dermatol. 1995 Aug;33(2 Pt 2):327-32. doi: 10.1016/0190-9622(95)91427-7.
Transfusion-associated graft-versus-host disease (TAGVHD) occurs in immunocompromised persons who receive nonirradiated blood products containing immunologically competent donor lymphocytes. TAGVHD occurs almost exclusively as an acute illness and has a very high mortality rate. We describe a patient with a long history of non-Hodgkin's lymphoma in whom acute TAGVHD developed after transfusion of packed red blood cells from two unrelated donors. TAGVHD developed despite pretreatment of the transfused units with white blood cell filters. The patient survived and subsequently had clinical manifestations typical of chronic cutaneous graft-versus-host disease. HLA phenotyping studies suggested that elements from both transfusion donors engrafted. TAGVHD is a rare but probably underdiagnosed disorder that, although usually fatal, may evolve into chronic graft-versus-host disease. Treatment of blood products with white blood cell filters does not appear adequate to prevent TAGVHD.
输血相关移植物抗宿主病(TAGVHD)发生于接受含有免疫活性供体淋巴细胞的未辐照血液制品的免疫功能低下者。TAGVHD几乎仅表现为急性疾病,死亡率极高。我们描述了一名有非霍奇金淋巴瘤病史的患者,其在输注来自两名无关供体的浓缩红细胞后发生了急性TAGVHD。尽管对输注的血液制品进行了白细胞过滤预处理,但仍发生了TAGVHD。该患者存活下来,随后出现了慢性皮肤移植物抗宿主病的典型临床表现。HLA表型研究表明,两名输血供体的成分均发生了植入。TAGVHD是一种罕见但可能诊断不足的疾病,虽然通常致命,但可能会演变为慢性移植物抗宿主病。用白细胞过滤器处理血液制品似乎不足以预防TAGVHD。