Stanley E D, Jackson G G, Dirda V A, Rubenis M
J Infect Dis. 1976 Jun;133 Suppl:A121-127. doi: 10.1093/infdis/133.supplement_2.a121.
Six controlled trials of a topical interferon inducer, N',N'-diotadecyl-N',N'-bis-(2-hydroxyethyl) propanediamine (CP 20961), against rhinovirus infection in volunteers were reviewed. Controls were the drug vehicle (which consisted of a mixture of polysorbate-80 in gylcerol and saline), saline only, and oral lactose. Multiple doses of the inducer given before challenge in any of three regimens reduced the symptomatic response to viral infection. Treatment with three doses of drug the day before challenge enhanced the interferon response to virus; four days of treatment with either the drug or its vehicle before challenge produced a refractoriness to further interferon induction. Both the drug and its vehicle were capable of inducing nasal interferon. When interferon was present at the time of viral inoculation, symptoms were reduced with or without an increase in the interferon response to infection. The rates of infection and illness were increased after a single dose of drug and decreased after a single dose of the vehicle alone.
对六项关于局部干扰素诱导剂N',N'-二十二烷基-N',N'-双(2-羟乙基)丙二胺(CP 20961)预防志愿者鼻病毒感染的对照试验进行了综述。对照组为药物赋形剂(由聚山梨酯-80、甘油和盐水的混合物组成)、仅用盐水以及口服乳糖。在三种方案中的任何一种中,在攻击前给予多剂量诱导剂可降低对病毒感染的症状反应。在攻击前一天用三剂药物治疗可增强对病毒的干扰素反应;在攻击前用药物或其赋形剂治疗四天会产生对进一步干扰素诱导的不应性。药物及其赋形剂均能够诱导鼻内干扰素。当在病毒接种时存在干扰素时,无论对感染的干扰素反应是否增加,症状都会减轻。单剂量药物后感染率和发病率增加,而单剂量赋形剂后则降低。