O'Reilly R J, Chibbaro A, Wilmot R, Lopez C
Ann N Y Acad Sci. 1977 Mar 4;284:161-70. doi: 10.1111/j.1749-6632.1977.tb21947.x.
Patients with herpes progenitalis recurring every 14--28 days were treated with levamisole 150 mg orally twice weekly in an open trial to evaluate the relationship between immunomodulation and clinical response. Eight of 12 patients studied for 4--9 months reported a decrease in the frequency of recurrences. Enhanced virus-specific lymphoproliferative responses were observed in six of eight patients reporting clinical improvement. Herpes-antigen-induced production of leucocyte migration inhibitory factor (LMIF) was similarly enhanced in these individuals. In the four patients reporting no improvement, virus-specific lymphoproliferative and LMIF-generating responses were either depressed or unchanged. No significant alterations in neutralizing antibody titers were observed in any of the patients. Alterations in virus-specific lymphocyte transformation and lymphokine generation observed in vitro thus correlate with changes in clinical course in a manner consistent with the proposed immunomodulatory function of levamisole.
在一项开放性试验中,对每14 - 28天复发一次的生殖器疱疹患者口服左旋咪唑150毫克,每周两次,以评估免疫调节与临床反应之间的关系。在接受研究4 - 9个月的12名患者中,有8名报告复发频率降低。在报告临床症状改善的8名患者中,有6名观察到病毒特异性淋巴细胞增殖反应增强。在这些个体中,疱疹抗原诱导的白细胞迁移抑制因子(LMIF)产生同样增强。在报告无改善的4名患者中,病毒特异性淋巴细胞增殖和产生LMIF的反应要么受到抑制,要么没有变化。在任何患者中均未观察到中和抗体滴度有显著改变。因此,体外观察到的病毒特异性淋巴细胞转化和淋巴因子产生的改变与临床病程的变化相关,其方式与左旋咪唑提出的免疫调节功能一致。