Kremsner P G, Neifer S, Schermuck S, Chaves M F, Sliwa K, Bienzle U
Landesinstitut für Tropenmedizin Berlin, Germany.
J Infect Dis. 1991 May;163(5):1161-3. doi: 10.1093/infdis/163.5.1161.
Most nonimmune patients with Plasmodium falciparum infection are no longer cured by such standard antimalarial drugs as chloroquine. Thus, alternative treatment regimens are necessary. A combination therapy was tested consisting of a subcurative dose of chloroquine and interferon-gamma (IFN-gamma) in BALB/c mice with lethal Plasmodium vinckei malaria. Treatment with either agent alone prolonged median survival by 1-2 days compared with placebo-treated mice. However, a combination of 80 micrograms of chloroquine given at the time of infection plus 1 x 10(4) units of IFN-gamma/day for 11 days (starting 3 days before infection) cured 83% of infected mice. Moreover, these mice showed solid immunity when challenged with the homologous strain of P. vinckei. However, when these mice were infected with the heterologous strain of Plasmodium berghei, the same degree of parasitemia developed as did in P. berghei-infected control mice. Thus, the combination of chemotherapy with the cytokine IFN-gamma leads to substantial improvement of antimalarial treatment and to a rapid development of strain-specific immunity in murine P. vinckei malaria.
大多数感染恶性疟原虫的非免疫患者不再能被氯喹等标准抗疟药物治愈。因此,需要替代治疗方案。在患有致死性文氏疟原虫疟疾的BALB/c小鼠中,测试了一种由亚治愈剂量的氯喹和干扰素-γ(IFN-γ)组成的联合疗法。与用安慰剂治疗的小鼠相比,单独使用任何一种药物治疗都能使中位生存期延长1至2天。然而,在感染时给予80微克氯喹加1×10⁴单位IFN-γ/天,持续11天(从感染前3天开始),可治愈83%的感染小鼠。此外,这些小鼠在用文氏疟原虫同源菌株攻击时表现出牢固的免疫力。然而,当这些小鼠感染伯氏疟原虫异源菌株时,其疟原虫血症程度与感染伯氏疟原虫的对照小鼠相同。因此,化疗与细胞因子IFN-γ的联合使用可显著改善抗疟治疗效果,并在小鼠文氏疟原虫疟疾中迅速产生菌株特异性免疫力。