Kolb Hans-Jochem, Schmid Christoph, Barrett A John, Schendel Dolores J
Hematopoietic Cell Transplantation, Dept of Medicine III, Clinical University of Munich-Grosshadern, Marchioninistr 15, 81377 Munich, Germany.
Blood. 2004 Feb 1;103(3):767-76. doi: 10.1182/blood-2003-02-0342. Epub 2003 Sep 4.
There is a strong graft-versus-leukemia (GVL) effect of allogeneic stem cell transplantation (SCT) due to elimination of tumor cells by alloimmune effector lymphocytes. When leukemia relapses after allogeneic SCT, donor lymphocyte transfusions (DLTs) can induce sustained remissions in some patients. This review summarizes the current status on clinical use of DLT, the basis of GVL reactions, problems associated with this therapy, and new strategies to improve DLT. Several multicenter surveys demonstrated that the GVL effect of DLT is most effective in chronic myelogenous leukemia (CML), whereas it is less pronounced in acute leukemia and myeloma. Cytokine stimulation to induce differentiation of myeloid progenitor cells or to up-regulate costimulatory molecules on tumor cells may improve the efficacy of DLT. Infections and graft-versus-host disease (GVHD) are major complications of DLT. Control of GVHD may be improved using suicide gene-modified T cells for DLT, allowing T-cell elimination if severe GVHD develops. Hopefully, in the future, GVL effect can be separated from GVHD through adoptive transfer of selected T cells that recognize leukemia-specific antigens or minor histocompatibility antigens, which are expressed predominantly on hematopoietic cells, thereby precluding attack of normal tissues. In patients with leukemia and lymphomas with fast progression, tumor growth may outpace development of effector T cells. Here it may be preferable to select stem cell transplant donors with HLA-mismatches that allow alloreactive natural killer cells, which appear early after transplantation, to retain their cytolytic function. New approaches for adoptive immune therapy of leukemia, which promise a better prognosis for these patients, are being developed.
由于同种异体免疫效应淋巴细胞消除肿瘤细胞,异基因干细胞移植(SCT)具有强大的移植物抗白血病(GVL)效应。异基因SCT后白血病复发时,供体淋巴细胞输注(DLT)可使部分患者获得持续缓解。本文综述了DLT临床应用的现状、GVL反应的基础、该治疗相关的问题以及改善DLT的新策略。多项多中心调查表明,DLT的GVL效应在慢性粒细胞白血病(CML)中最为有效,而在急性白血病和骨髓瘤中则不太明显。细胞因子刺激诱导髓系祖细胞分化或上调肿瘤细胞上的共刺激分子可能会提高DLT的疗效。感染和移植物抗宿主病(GVHD)是DLT的主要并发症。使用自杀基因修饰的T细胞进行DLT可能会改善GVHD的控制,若发生严重GVHD可使T细胞消除。有望在未来,通过过继转移识别白血病特异性抗原或次要组织相容性抗原的特定T细胞来分离GVL效应和GVHD,这些抗原主要在造血细胞上表达,从而避免对正常组织的攻击。在白血病和进展迅速的淋巴瘤患者中,肿瘤生长可能超过效应T细胞的发育。在此情况下,选择与HLA不匹配的干细胞移植供体可能更可取,这可使移植后早期出现的同种异体反应性自然杀伤细胞保留其细胞溶解功能。正在开发有望改善这些患者预后的白血病过继免疫治疗新方法。