Orholm M, Pedersen C, Mathiesen L, Dowd P, Nielsen J O
Department of Infectious Diseases, University of Copenhagen, Hvidovre Hospital, Denmark.
AIDS. 1989 Feb;3(2):97-100. doi: 10.1097/00002030-198902000-00008.
On the basis of the observations that HIV antigenaemia indicates a high risk of progression to AIDS and that zidovudine and alpha-interferon act synergistically against HIV replication in vitro, we performed a pilot trial including 12 HIV-infected asymptomatic patients with detectable p24 antigen in serum. The patients received low-dose lymphoblastoid alpha-interferon alone for 4 weeks followed by a combination of interferon and low-dose zidovudine for a further 16 weeks. The median p24 antigen level decreased significantly (P less than 0.01), the decrease being most pronounced at week 5. Decreases in haemoglobin and neutrophil counts were observed. Four patients required reduction of the zidovudine dose and three patients were transfused. In conclusion, the drug combination was capable of reducing the serum level of HIV p24 antigen and it was tolerated by the patients. Further studies are required to evaluate the clinical implications of these observations.
HIV抗原血症表明发展为艾滋病的高风险,以及齐多夫定和α干扰素在体外对HIV复制具有协同作用,我们进行了一项试点试验,纳入了12例血清中可检测到p24抗原的HIV感染无症状患者。患者先单独接受低剂量淋巴母细胞α干扰素治疗4周,随后干扰素与低剂量齐多夫定联合治疗16周。p24抗原水平中位数显著下降(P<0.01),在第5周时下降最为明显。观察到血红蛋白和中性粒细胞计数下降。4例患者需要减少齐多夫定剂量,3例患者接受了输血。总之,该药物组合能够降低HIV p24抗原的血清水平,且患者能够耐受。需要进一步研究来评估这些观察结果的临床意义。