Giralt S, Hester J, Huh Y, Hirsch-Ginsberg C, Rondón G, Seong D, Lee M, Gajewski J, Van Besien K, Khouri I, Mehra R, Przepiorka D, Körbling M, Talpaz M, Kantarjian H, Fischer H, Deisseroth A, Champlin R
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77031, USA.
Blood. 1995 Dec 1;86(11):4337-43.
Donor lymphocyte infusions can reinduce complete remission in the majority of patients with chronic myelogenous leukemia (CML) who relapse into chronic phase after allogeneic bone marrow transplantation (BMT). Such infusions are associated with a high incidence of graft-versus-host disease (GVHD) and marrow aplasia. BMT using selective depletion of CD8+ lymphocytes from donor cells reduces the incidence of GVHD without an increase in leukemia relapse. We hypothesized that infusion of CD8-depleted donor peripheral blood lymphocytes could also reinduce complete remissions with a lesser potential to produce symptomatic GVHD in patients with CML who relapsed after allogeneic BMT. Ten patients with Ph(+) CML who relapsed a median of 353 days after BMT (range, 82 to 1,096 days) received donor lymphocyte infusions depleted of CD8+ cells. Nine patients received a single infusion and 1 received two infusions. Four patients were treated while in chronic phase with clonal evolution, 2 during accelerated phase, 3 during blast crisis, and 1 in a cytogenetic relapse. A mean of 0.9 +/- 0.3 x 10(8) mononuclear cells/kg were infused, containing 0.6 +/- 0.4 x 10(6) CD3+CD8+ cells/kg. Six patients achieved hematologic and cytogenetic remission at 4, 8, 11, 15, 39, and 54 weeks after lymphocyte infusion. Two patients developed > or = grade II acute GVHD, and 1 patient developed mild chronic GVHD. We conclude that donor lymphocyte infusions depleted of CD8+ cells can induce remissions with a low rate of severe acute GVHD in patients with CML who relapse after allogeneic BMT, supporting the hypothesis that CD8+ lymphocytes are important effectors of GVHD, but may not be essential for the graft-versus-leukemia effect against this disease. Further controlled studies are required to confirm these preliminary observations.
供体淋巴细胞输注可使大多数在异基因骨髓移植(BMT)后复发进入慢性期的慢性粒细胞白血病(CML)患者再次完全缓解。这种输注与移植物抗宿主病(GVHD)和骨髓再生障碍的高发生率相关。使用供体细胞选择性去除CD8 +淋巴细胞的BMT可降低GVHD的发生率,而不会增加白血病复发率。我们推测,输注去除CD8的供体外周血淋巴细胞也可使异基因BMT后复发的CML患者再次完全缓解,且产生有症状GVHD的可能性较小。10例Ph(+) CML患者在BMT后中位353天(范围82至1096天)复发,接受了去除CD8 +细胞的供体淋巴细胞输注。9例患者接受了单次输注,1例接受了两次输注。4例患者在慢性期伴克隆演变时接受治疗,2例在加速期,3例在急变期,1例处于细胞遗传学复发期。平均输注0.9±0.3×10(8)个单核细胞/kg,其中含0.6±0.4×10(6)个CD3 + CD8 +细胞/kg。6例患者在淋巴细胞输注后4、8、11、15、39和54周达到血液学和细胞遗传学缓解。2例患者发生≥II级急性GVHD,1例患者发生轻度慢性GVHD。我们得出结论,去除CD8 +细胞的供体淋巴细胞输注可使异基因BMT后复发的CML患者诱导缓解,且严重急性GVHD发生率低,支持CD8 +淋巴细胞是GVHD重要效应细胞,但可能不是针对该疾病的移植物抗白血病效应所必需的这一假说。需要进一步的对照研究来证实这些初步观察结果。