Mayer R A, Sergios P A, Coonan K, O'Brien L
R. A. Mayer Clinic, Department of Research and Development, North Miami, Florida.
Eur J Clin Invest. 1992 Feb;22(2):113-22. doi: 10.1111/j.1365-2362.1992.tb01944.x.
Twenty patients with the acquired immunodeficiency syndrome (AIDS), AIDS-related complex (ARC) or asymptomatic HIV infection (HIV+) were given 20 mcg kg-3 trichosanthin (TCS; 'Compound Q'), a ribosome-inactivating protein with in vitro antiviral activity against human immunodeficiency virus (HIV) once every four weeks for up to 12 weeks. With the concurrent administration of prostaglandin inhibitors, the drug was moderately well tolerated, with most subjects experiencing mild arthralgia, hives and malaise. Additionally, four patients experienced neurological complications which resolved spontaneously without intervention. Four of 20 subjects in this open label pilot study showed progressive although transient reductions in viral activity as measured by p-24 antigen level decreases. Subjects also experienced decreases in levels of beta 2-microglobulin. Ten HIV+ and healthy ARC subjects demonstrated improved immunological status as measured by significant increases in percentage of CD4+ cells and augmentations in delayed hypersensitivity reactions. Eight of 20 subjects reported improved appetites and increased energy levels. The group as a whole had a weight gain of 3.2 kg. Eight of 20 subjects who presented with persistent generalized lymphadenopathy exhibited a marked diminution in the size of their lymph nodes after the first treatment. No subject who presented with oral candidiasis experienced an improvement in that condition. We conclude that, in the short term, TCS seems to have the ability to reduce viral activity and improve certain symptoms in healthy ARC patients and HIV + asymptomatics although it may not be able to restore immune competence in persons with advanced AIDS or poor prognosis ARC. Additionally, the drug may pose a special risk for patients with HIV-related dementia.
20名患有获得性免疫缺陷综合征(AIDS)、AIDS相关综合征(ARC)或无症状HIV感染(HIV+)的患者,每四周接受一次20微克/千克的天花粉蛋白(TCS;“复方Q”),这是一种核糖体失活蛋白,具有体外抗人类免疫缺陷病毒(HIV)的活性,治疗期长达12周。在同时使用前列腺素抑制剂的情况下,该药物耐受性中等良好,大多数受试者出现轻度关节痛、荨麻疹和不适。此外,有4名患者出现神经系统并发症,但未经干预自行缓解。在这项开放标签的初步研究中,20名受试者中有4名显示,通过p-24抗原水平降低来衡量,病毒活性虽有进展但呈短暂下降。受试者的β2-微球蛋白水平也有所降低。10名HIV+和健康的ARC受试者显示免疫状态有所改善,表现为CD4+细胞百分比显著增加以及迟发型超敏反应增强。20名受试者中有8名报告食欲改善、精力增加。整个组体重增加了3.2千克。20名出现持续性全身性淋巴结病的受试者中有8名在首次治疗后淋巴结大小明显缩小。所有出现口腔念珠菌病的受试者病情均未改善。我们得出结论,短期内,天花粉蛋白似乎有能力降低健康的ARC患者和HIV+无症状感染者的病毒活性并改善某些症状,尽管它可能无法恢复晚期AIDS患者或预后不良的ARC患者的免疫能力。此外,该药物可能给患有HIV相关痴呆的患者带来特殊风险。