Garaci E, Rocchi G, Perroni L, D'Agostini C, Soscia F, Grelli S, Mastino A, Favalli C
Department of Experimental Medicine and Biochemical Sciences, University of Rome Tor Vergata, Italy.
Int J Clin Lab Res. 1994;24(1):23-8. doi: 10.1007/BF02592405.
We have investigated the effects of combination therapy with thymosin alpha 1 and natural human lymphoblastoid interferon-alpha in human immunodeficiency virus infection and have shown that in vitro this combination treatment: (1) synergistically stimulated the cytotoxic activity against natural killer-sensitive target cells of lymphocytes collected from human immunodeficiency virus-infected donors and (2) did not interfere with the antiviral activity of zidovudine. We thus studied the effects of combination therapy with thymosin alpha 1, interferon-alpha and zidovudine in patients with CD4+ lymphocytes ranging from 200 to 500/mm3 in a randomized non-blinded study and found that the treatment was well tolerated after 12 months of therapy and was associated with a substantial increase in the number and function of CD4+ T cells. A similar effect was not observed in human immunodeficiency virus patients treated with zidovudine alone or associated with single agents. These data suggest the need for a controlled, double-blind clinical trial, recently initiated with the approval and the support of the Italian Ministry of Health.
我们研究了胸腺肽α1与天然人淋巴母细胞干扰素-α联合治疗对人类免疫缺陷病毒感染的影响,并表明在体外这种联合治疗:(1)协同刺激了从人类免疫缺陷病毒感染供体收集的淋巴细胞对自然杀伤敏感靶细胞的细胞毒活性,(2)不干扰齐多夫定的抗病毒活性。因此,我们在一项随机非盲研究中,对CD4 +淋巴细胞计数在200至500/mm³之间的患者,研究了胸腺肽α1、干扰素-α与齐多夫定联合治疗的效果,发现治疗12个月后耐受性良好,且与CD4 + T细胞数量和功能的显著增加相关。在单独使用齐多夫定或与单一药物联合治疗的人类免疫缺陷病毒患者中未观察到类似效果。这些数据表明需要进行一项对照双盲临床试验,该试验最近已在意大利卫生部的批准和支持下启动。