Hammer S M, Gillis J M
Department of Medicine, New England Deaconess Hospital, Boston, Massachusetts.
Antimicrob Agents Chemother. 1987 Jul;31(7):1046-50. doi: 10.1128/AAC.31.7.1046.
The ability of granulocyte-macrophage colony-stimulating factor (GM-CSF) and 3'-azido-3'-deoxythymidine (AZT) to inhibit human immunodeficiency virus (HIV) in the U-937 monocytic cell line was examined. Acutely HIV-infected U-937 cells were exposed to GM-CSF (0.03, 0.3, 3.0, or 30.0 U/ml) and AZT (0.1, 1.0, or 10.0 microM) alone and in combination for 14 to 17 days. Reverse transcriptase activity in the supernatant, the percentage of cells expressing viral antigens by indirect immunofluorescence, and the 50% tissue culture infectious dose per milliliter of supernatant were determined to assess the level of viral replication in treated and control cultures. By the fractional-product method of analysis, nearly all combinations of GM-CSF and AZT synergistically inhibited HIV replication by these three measurements. The most effective combinations were 30 U of GM-CSF per ml with 0.1, 1.0, or 10.0 microM AZT. These treatments resulted in no reverse transcriptase activity in the supernatants, less than 1% immunofluorescent positive cells, and less than 8 50% tissue culture infectious doses per ml in the absence of cytotoxicity. Despite this degree of suppression, productive viral replication returned in all cultures within 4 to 10 days after drug removal. Combined therapy with GM-CSF and AZT merits consideration in the approach to HIV-associated illnesses.
研究了粒细胞-巨噬细胞集落刺激因子(GM-CSF)和3'-叠氮-3'-脱氧胸苷(AZT)对U-937单核细胞系中人类免疫缺陷病毒(HIV)的抑制能力。将急性HIV感染的U-937细胞单独及联合暴露于GM-CSF(0.03、0.3、3.0或30.0 U/ml)和AZT(0.1、1.0或10.0 μM)中14至17天。测定上清液中的逆转录酶活性、通过间接免疫荧光法表达病毒抗原的细胞百分比以及每毫升上清液的50%组织培养感染剂量,以评估处理组和对照组培养物中的病毒复制水平。通过分数乘积分析法,GM-CSF和AZT的几乎所有组合通过这三项测量均协同抑制HIV复制。最有效的组合是每毫升30 U的GM-CSF与0.1、1.0或10.0 μM的AZT。这些处理导致上清液中无逆转录酶活性,免疫荧光阳性细胞少于1%,且在无细胞毒性的情况下每毫升少于8个50%组织培养感染剂量。尽管有这种程度的抑制,但在去除药物后4至10天内,所有培养物中均恢复了有生产性的病毒复制。GM-CSF和AZT联合疗法在治疗HIV相关疾病的方法中值得考虑。