Antin J H, Smith B R, Ewenstein B M, Arceci R J, Lipton J M, Page P L, Rappeport J M
Blood. 1986 Jan;67(1):160-3.
We prospectively documented the development of a fatal, secondarily acquired severe immunodeficiency in a 19-year-old man who underwent uncomplicated bone marrow transplantation. He had no graft v host disease (GVHD) and had normal recovery of his immune system as determined by lymphocyte phenotyping, mitogenic responses of his peripheral blood lymphocytes, and his ability to secrete immunoglobulin. This alteration in immunity was associated with the acquisition of antibody to HTLV-III. His only risk factor for the development of HTLV-III infection was the transfusions he had received during the transplant and recovery period. Two of his 54 transfusions were from an asymptomatic individual at high risk for acquired immunodeficiency syndrome (AIDS), who was subsequently found to be seropositive for anti-HTLV-III and from whom HTLV-III was isolated. The loss of immunocompetence in patients without chronic GVHD disease is unusual, and our data support the view that this patient's immunodeficiency was due to HTLV-III. When bone marrow transplant recipients without chronic GVHD develop late opportunistic infections, consideration should be given to transfusion-associated AIDS.
我们前瞻性地记录了一名19岁男性在接受无并发症骨髓移植后发生的致命性、继发性获得性严重免疫缺陷的发展过程。他没有移植物抗宿主病(GVHD),通过淋巴细胞表型分析、外周血淋巴细胞的有丝分裂反应以及他分泌免疫球蛋白的能力确定其免疫系统恢复正常。这种免疫改变与获得抗HTLV-III抗体有关。他发生HTLV-III感染的唯一危险因素是他在移植和恢复期间接受的输血。他的54次输血中有2次来自一名患获得性免疫缺陷综合征(AIDS)风险高的无症状个体,该个体随后被发现抗HTLV-III血清学阳性,且从中分离出了HTLV-III。没有慢性GVHD疾病的患者免疫能力丧失并不常见,我们的数据支持该患者免疫缺陷是由HTLV-III引起的观点。当没有慢性GVHD的骨髓移植受者发生晚期机会性感染时,应考虑输血相关的AIDS。