Roney C S, Rossi C R, Smith P C, Lauerman L C, Spano J S, Hanrahan L A, William J C
Am J Vet Res. 1985 Jun;46(6):1251-5.
Human leukocyte A interferon was evaluated for its ability to prevent infectious bovine rhinotracheitis virus-induced respiratory tract disease in cattle. Weanling calves were treated daily for 1 week with 50 X 10(6) U of interferon, intranasally (by nebulization) and IM, and inoculated with infectious bovine rhinotracheitis virus on the first day of treatment. Respiratory tract disease was less severe in treated as compared with nontreated calves which were given only infectious bovine rhinotracheitis virus, and infection in the treated calves occurred later than in the untreated calves. Viral shedding and appearance of viral neutralizing antibodies occurred later in treated calves than in calves given only virus. Because several calves in a treatment group were housed together, whether the late appearance of infection in some interferon-treated calves was due to emergence of suppressed virus or to horizontal transmission from calves shedding virus could not be determined. One calf in the interferon-treated group developed antibody to human interferon and a few treated calves had transient elevation of hepatic enzymes. Interferon-treated calves developed a high temperature which subsided on termination of treatment. Production of disease was considerably dependent on the amount of virus and interferon given, since calves given 300 times more virus and approximately half as much interferon showed no evidence of protection against infection.
对人白细胞A干扰素预防牛传染性鼻气管炎病毒引起的牛呼吸道疾病的能力进行了评估。断奶小牛每天经鼻(通过雾化)和肌肉注射50×10⁶单位干扰素,持续1周,并在治疗的第一天接种牛传染性鼻气管炎病毒。与仅接种牛传染性鼻气管炎病毒的未治疗小牛相比,治疗后的小牛呼吸道疾病症状较轻,且治疗组小牛的感染发生时间晚于未治疗小牛。治疗组小牛的病毒排出和病毒中和抗体出现时间均晚于仅接种病毒的小牛。由于一个治疗组中的几头小牛饲养在一起,因此无法确定一些经干扰素治疗的小牛感染出现较晚是由于被抑制病毒的出现,还是由于从排毒小牛的水平传播。干扰素治疗组中有一头小牛产生了针对人干扰素的抗体,一些治疗小牛的肝酶出现短暂升高。经干扰素治疗的小牛体温升高,治疗结束后体温下降。疾病的产生在很大程度上取决于所给予的病毒量和干扰素量,因为接种300倍以上病毒且干扰素量约为一半的小牛没有显示出对感染的保护迹象。