Künzi M S, Farzadegan H, Margolick J B, Vlahov D, Pitha P M
Oncology Center, Johns Hopkins University, Baltimore, Maryland.
J Infect Dis. 1995 Apr;171(4):822-8. doi: 10.1093/infdis/171.4.822.
Human immunodeficiency virus (HIV) primary isolates, derived from donors at various stages of HIV infection, were assayed for their sensitivity to interferon (IFN)-alpha 2 in vitro. These isolates displayed a broad range of sensitivity to IFN-alpha 2. The prevalence of IFN-alpha 2 resistance was low in the absence of AIDS but dramatically increased once HIV infection progressed to AIDS. Although there was no linear correlation between the percentage of IFN-alpha 2 inhibition in vitro and the CD4 cell number in vivo or the level of endogenous IFN-alpha, serum IFN-alpha levels were higher in donors with AIDS and were associated with low CD4 cell numbers. Thus, circulating IFN-alpha appeared to either promote resistance or favor survival of IFN-alpha resistant variants. IFN-alpha 2 resistance was neither limited to a particular cell tropism nor enhanced by therapy with zidovudine. Sequential analysis indicated that reversion to IFN-alpha 2 sensitivity could occur during the course of infection.
对来自处于人类免疫缺陷病毒(HIV)感染不同阶段供体的HIV原始分离株进行了体外干扰素(IFN)-α2敏感性检测。这些分离株对IFN-α2表现出广泛的敏感性。在没有艾滋病的情况下,IFN-α2耐药的发生率较低,但一旦HIV感染发展为艾滋病,其发生率会急剧上升。尽管体外IFN-α2抑制百分比与体内CD4细胞数量或内源性IFN-α水平之间没有线性相关性,但艾滋病供体的血清IFN-α水平较高,且与低CD4细胞数量相关。因此,循环中的IFN-α似乎要么促进耐药性,要么有利于IFN-α耐药变异株的存活。IFN-α2耐药性既不限于特定的细胞嗜性,也不会因齐多夫定治疗而增强。序列分析表明,在感染过程中可能会出现恢复对IFN-α2敏感性的情况。