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更昔洛韦联合齐多夫定在体外和体内抗巨细胞病毒的疗效。

Efficacy of ganciclovir in combination with zidovudine against cytomegalovirus in vitro and in vivo.

作者信息

Freitas V R, Fraser-Smith E B, Chiu S, Michelson S, Schatzman R C

机构信息

Syntex Research, Palo Alto, CA 94304.

出版信息

Antiviral Res. 1993 Aug;21(4):301-15. doi: 10.1016/0166-3542(93)90009-8.

Abstract

In cultured MRC-5 cells, ganciclovir (GCV) alone had good activity against both the established AD169 strain (IC50 8 and 9 microM) and a clinical isolate (IC50 14 microM) of human cytomegalovirus (CMV), while 3'-azido-3'-deoxythymidine (AZT) was relatively inactive [IC50 508 and > 800 (AD169 strain); > 800 microM (clinical isolate)]. When reductions in plaques were compared against reductions in the cellular metabolism of MTT at all GCV and AZT combination concentrations using an improved 3-dimensional linear regression analysis, AZT had an additive effect on the antiviral activity of GCV against the AD169 strain and potentiated the antiviral activity of GCV against the clinical isolate. Calculations showed that, in the presence of 50 microM AZT, the anti-CMV activity of GCV was unchanged for the AD169 strain, whereas the activity of GCV was increased approximately 5-10-fold for the clinical isolate. An increase in GCV efficacy for the AD169 strain first became apparent at 100 microM AZT with an approximately 3-fold increase in activity. In Swiss-Webster mice, the anti-CMV activity of GCV against murine CMV was unaffected when administered in combination with AZT. GCV given alone subcutaneously had an ED50 of 6 mg/kg which was unaffected by daily intraperitoneal doses of 320 mg/kg AZT. These results suggest that AZT will not adversely affect the efficacy of GCV against CMV in HIV-positive, non-neutropenic patients.

摘要

在培养的MRC-5细胞中,更昔洛韦(GCV)单独使用时对人巨细胞病毒(CMV)的标准株AD169(IC50为8和9微摩尔)和一株临床分离株(IC50为14微摩尔)均具有良好的活性,而3'-叠氮-3'-脱氧胸苷(AZT)相对无活性[IC50为508和>800(AD169株);>800微摩尔(临床分离株)]。当使用改进的三维线性回归分析比较所有GCV和AZT组合浓度下蚀斑减少量与MTT细胞代谢减少量时,AZT对GCV抗AD169株的抗病毒活性具有相加作用,并增强了GCV对临床分离株的抗病毒活性。计算表明,在存在50微摩尔AZT的情况下,GCV对AD169株的抗CMV活性未改变,而对临床分离株GCV的活性增加了约5至10倍。对于AD169株,GCV疗效的增加在100微摩尔AZT时首次明显显现,活性增加了约3倍。在瑞士-韦伯斯特小鼠中,GCV与AZT联合给药时,其对鼠巨细胞病毒的抗CMV活性未受影响。单独皮下给予GCV的ED50为6毫克/千克,不受每日腹腔注射320毫克/千克AZT的影响。这些结果表明,AZT不会对HIV阳性、非中性粒细胞减少患者中GCV抗CMV的疗效产生不利影响

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