Iuchi Yasuyuki, Torimoto Yoshihiro, Sato Kazuya, Tamura Yasuaki, Jimbo Junko, Inamura Junki, Shindo Motohiro, Ikuta Katsuya, Ohnishi Kouhei, Kohgo Yutaka
Division of Gastroenterology and Hematology/Oncology, Department of Medicine Asahikawa Medical College, Asahikawa, Japan.
Int J Hematol. 2006 Dec;84(5):449-58. doi: 10.1532/IJH97.06003.
We have reported that immunotherapy using leukemia cell-derived heat shock proteins (HSPs) is effective against minimal residual disease (MRD) after syngeneic stem cell transplantation (SCT) in mice. However, leukemia patients after SCT are usually immunocompromised and immunologically tolerant to leukemia cells. We investigated whether the use of dendritic cells (DCs) in combination with HSP70 enhances cytotoxicity against B-cell leukemia cell line A20 in mice after syngeneic SCT. All unimmunized mice died of leukemia early after A20 cell inoculation, whereas mice immunized with HSP70 or HSP70-pulsed DCs survived significantly longer. Although only 60% of the HSP70-immunized mice survived, all mice immunized with HSP70-pulsed DCs survived without MRD. In addition, the cytotoxicities against A20 cells for splenocytes from mice immunized with HSP70-pulsed DCs were significantly higher than those of HSP70-immunized mice, and the cytotoxicities against A20 cells were significantly blocked by anti-CD8 antibody and by major histocompatibility complex class I antibody, but not by anti-CD4 antibody. Moreover, abnormalities were detected in neither the biochemical data nor the histopathologic findings. These findings indicate that the combined use of DCs and leukemia cell-derived HSP70 enhances the antileukemia effect by inducing the specific cytotoxicities of CD8+ cytotoxic T-cells, thereby eradicating MRD effectively and safely, even in an immunocompromised state after syngeneic SCT. This approach may thus be useful for further application of HSP in leukemia patients after autologous SCT.
我们已经报道,使用白血病细胞衍生的热休克蛋白(HSPs)进行免疫治疗对小鼠同基因干细胞移植(SCT)后的微小残留病(MRD)有效。然而,SCT后的白血病患者通常免疫功能低下且对白血病细胞具有免疫耐受性。我们研究了在同基因SCT后,将树突状细胞(DCs)与HSP70联合使用是否能增强对小鼠B细胞白血病细胞系A20的细胞毒性。所有未免疫的小鼠在接种A20细胞后早期死于白血病,而用HSP70或HSP70脉冲DCs免疫的小鼠存活时间显著延长。尽管只有60%的HSP70免疫小鼠存活,但所有用HSP70脉冲DCs免疫的小鼠均存活且无MRD。此外,用HSP70脉冲DCs免疫的小鼠脾细胞对A20细胞的细胞毒性显著高于HSP70免疫的小鼠,并且对A20细胞的细胞毒性被抗CD8抗体和主要组织相容性复合体I类抗体显著阻断,但不被抗CD4抗体阻断。此外,生化数据和组织病理学检查结果均未检测到异常。这些发现表明,DCs与白血病细胞衍生的HSP70联合使用可通过诱导CD8 + 细胞毒性T细胞的特异性细胞毒性来增强抗白血病作用,从而即使在同基因SCT后的免疫功能低下状态下也能有效且安全地根除MRD。因此,这种方法可能有助于HSP在自体SCT后白血病患者中的进一步应用。