Urbanitz D, Büchner T, Pielken H, van de Loo J
Klin Wochenschr. 1983 Oct 3;61(19):947-54. doi: 10.1007/BF01550267.
Patients with AML in complete remission (CR) are immunosuppressed; remission lymphocytes of at least a part of the patients are able to recognize autologous leukemic blasts; the CR represents a minimal residual disease. Thus, important conditions for a potentially successful active immunotherapy are given. Results of most earlier randomized trials on immunotherapy revealed some, but limited benefit with respect to survival. Encouraging effects, however, have been achieved by immunizing CR patients with high-dose neuraminidase-treated allogeneic blasts. Because these data have not been confirmed until now we recently initiated a randomized study utilizing identical treatment protocols. The preliminary results of the ongoing study still do not allow to draw any firm conclusions. Specific monoclonal antibodies or autologous cytotoxic T-cells may be useful tools for future immunotherapy of AML.
处于完全缓解(CR)状态的急性髓系白血病(AML)患者存在免疫抑制;至少部分患者的缓解期淋巴细胞能够识别自体白血病母细胞;完全缓解代表微小残留病。因此,具备了潜在成功的主动免疫治疗的重要条件。大多数早期免疫治疗随机试验的结果显示,在生存方面有一些但有限的益处。然而,通过用高剂量神经氨酸酶处理的同种异体母细胞免疫完全缓解患者已取得了令人鼓舞的效果。由于这些数据至今尚未得到证实,我们最近启动了一项采用相同治疗方案的随机研究。正在进行的研究的初步结果仍无法得出任何确凿结论。特异性单克隆抗体或自体细胞毒性T细胞可能是未来AML免疫治疗的有用工具。