Weck P K, Leventhal B G, Brand C, Finter N B
Burroughs Wellcome Company, Research Triangle Park, NC 27709.
J Interferon Res. 1989 Sep;9 Suppl 1:S37-43.
Sera obtained from 612 patients enrolled in 40 different clinical trials with an interferon-alpha-n1 (IFN-alpha-n1) preparation have been tested for neutralizing activity against this IFN in a cytopathic effect inhibition assay. Positive samples were assayed in triplicate. Of 391 patients treated for human papillomavirus infections, 13 developed neutralizing antibodies (3.3%); two suffering from condylomata acuminata and 11 from juvenile laryngeal papillomatosis (JLP). None has positive titers prior to receiving IFN-alpha-n1 and none appeared to lose the benefits of IFN treatment. Serial specimens from four JLP patients demonstrated that titers rose during IFN treatment and declined postherapy. None of the 221 cancer patients from whom serum samples were available had positive titers. The overall incidence of IFN neutralizing sera from these IFN-alpha-n1 recipients was 2.1%.
从参与40项不同临床试验的612名患者中获取的血清,采用细胞病变效应抑制试验检测了其对干扰素α-n1(IFN-α-n1)制剂的中和活性。阳性样本进行了三次重复检测。在391例接受人乳头瘤病毒感染治疗的患者中,13例产生了中和抗体(3.3%);2例患有尖锐湿疣,11例患有青少年喉乳头瘤病(JLP)。在接受IFN-α-n1治疗前,无一例中和抗体滴度呈阳性,且似乎无一例失去IFN治疗的益处。来自4例JLP患者的系列样本显示,中和抗体滴度在IFN治疗期间升高,治疗后下降。在可获取血清样本的221例癌症患者中,无一例中和抗体滴度呈阳性。这些IFN-α-n1接受者中IFN中和血清的总体发生率为2.1%。