Suehiro Y, Muta K, Umemura T, Motomura S, Nishimura J, Nawata H, Kimura N
Third Department of Internal Medicine, Faculty of Medicine, Kyushu University.
Rinsho Ketsueki. 1999 Jan;40(1):40-5.
Hematologic relapse of chronic myeloid leukemia developed in 37-year-old man 255 days after allogeneic bone marrow transplantation. The patient received a donor lymphocyte transfusion (DLT) twice at a dose of 5 x 10(6)/kg T cells. He achieved complete cytogenetic response (CCR) 14 weeks after DLT, and has remained in a CCR state for 17 months. Neither acute nor chronic graft-versus-host disease (GVHD) was observed. Natural killer (NK) cell activity was elevated. Also, analysis of the T cell receptor (TCR) repertoire disclosed oligoclonal expansion of T cells of the TCR V beta and J beta subfamilies. These observations provide evidence for the clonal expansion of allogeneic T cells that are capable of mediating antileukemic activity without causing GVHD.
一名37岁男性在异基因骨髓移植后255天出现慢性髓性白血病血液学复发。该患者接受了两次供体淋巴细胞输注(DLT),剂量为5×10(6)/kg T细胞。DLT后14周他实现了完全细胞遗传学缓解(CCR),并已处于CCR状态17个月。未观察到急性或慢性移植物抗宿主病(GVHD)。自然杀伤(NK)细胞活性升高。此外,T细胞受体(TCR)库分析显示TCR Vβ和Jβ亚家族的T细胞出现寡克隆扩增。这些观察结果为能够介导抗白血病活性而不引起GVHD的同种异体T细胞的克隆扩增提供了证据。