Hendrix C W, Margolick J B, Petty B G, Markham R B, Nerhood L, Farzadegan H, Ts'o P O, Lietman P S
Department of Medicine, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Maryland 21205.
Antimicrob Agents Chemother. 1993 Mar;37(3):429-35. doi: 10.1128/AAC.37.3.429.
Poly(I):poly(C12U) (mismatched double-stranded RNA; atvogen), an interferon inducer, is active against human immunodeficiency virus in vitro. To determine the extent and duration of the biologic effects of poly(I):poly(C12U), we administered a single dose of the drug to healthy volunteers in a randomized, double-blind, placebo-controlled 2-week crossover study. We analyzed blood for alpha and gamma interferons, neopterin, 2',5'-oligoadenylate synthetase, lymphocyte surface markers, lymphocyte proliferation after exposure to soluble antigens and mitogens, and natural killer cell activity. Minimal biologic effects were observed after administration of a single 200-mg dose to four volunteers; therefore, the dose was increased to 600 mg in 10 subjects. Only neopterin levels and symptoms were greater after administration of 600 mg of poly(I):poly(C12U) than after administration of placebo (Wilcoxon signed rank sum test, P = 0.06). A definite response in 2',5'-oligoadenylate synthetase activity, however, was seen in a few subjects. Neither alpha nor gamma interferon was detectable in serum after poly(I):poly(C12U) dosing. The neopterin changes after administration of poly(I):poly(C12U) were similar at both poly(I):poly(C12U) dose levels, with an early decrease at 6 h, a peak at 1 day, and a gradual decrease toward the baseline over the following 3 days. A mild flu-like syndrome occurred in one-half of the subjects following administration of poly(I):poly(C12U) and in only one subject following administration of placebo. This syndrome resolved within 16 h after poly(I):poly(C12U) dosing. We conclude that poly(I):poly(C12U) does not induce measurable levels of interferon and causes only minimal biologic or toxic effects among those parameters measured after administration of a single dose in the 200- to 600-mg dose range in health volunteers.
聚胞苷酸(12U)(错配双链RNA;阿特沃根)是一种干扰素诱导剂,在体外对人类免疫缺陷病毒具有活性。为了确定聚肌苷酸:聚胞苷酸(12U)的生物学效应程度和持续时间,我们在一项随机、双盲、安慰剂对照的2周交叉研究中,给健康志愿者单次服用该药物。我们分析了血液中的α和γ干扰素、新蝶呤、2',5'-寡腺苷酸合成酶、淋巴细胞表面标志物、接触可溶性抗原和丝裂原后的淋巴细胞增殖以及自然杀伤细胞活性。给4名志愿者单次服用200毫克剂量后,观察到的生物学效应极小;因此,在10名受试者中将剂量增加到600毫克。服用600毫克聚肌苷酸:聚胞苷酸(12U)后,只有新蝶呤水平和症状比服用安慰剂后更明显(威尔科克森符号秩和检验,P = 0.06)。然而,在少数受试者中观察到2',5'-寡腺苷酸合成酶活性有明确反应。服用聚肌苷酸:聚胞苷酸(12U)后,血清中未检测到α或γ干扰素。在两个聚肌苷酸:聚胞苷酸(12U)剂量水平下,服用聚肌苷酸:聚胞苷酸(12U)后的新蝶呤变化相似,6小时时早期下降,1天时达到峰值,随后3天逐渐降至基线。服用聚肌苷酸:聚胞苷酸(12U)后,一半受试者出现轻度流感样综合征,服用安慰剂后只有一名受试者出现。该综合征在服用聚肌苷酸:聚胞苷酸(12U)后16小时内消退。我们得出结论,在健康志愿者中,单次服用200至600毫克剂量范围内的聚肌苷酸:聚胞苷酸(12U)后,其不会诱导可测量水平的干扰素,并且在测量的参数中仅引起最小的生物学或毒性效应。