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在口服阿昔洛韦治疗的安慰剂对照试验中急性带状疱疹的水痘-带状疱疹特异性免疫反应

Varicella-zoster-specific immune responses in acute herpes zoster during a placebo-controlled trial of oral acyclovir therapy.

作者信息

Mitchell C D, Gehrz R C, Balfour H H

出版信息

Diagn Microbiol Infect Dis. 1986 Jul;5(2):113-26. doi: 10.1016/0732-8893(86)90113-6.

Abstract

During a placebo-controlled trial of oral acyclovir therapy for acute zoster in immunocompetent patients, we examined the blastogenic response of peripheral blood mononuclear cells and antibody titers in both placebo and acyclovir recipients to determine whether the drug affected the cell-mediated or humoral immune responses. Proliferative responses to mitogens and two dilutions of varicella-zoster virus antigen were not inhibited when fresh peripheral blood mononuclear cells were simultaneously tested in autologous sera collected before and on day 7 of a 10-day course of 2 g/day of oral acyclovir (plasma drug levels averaged 4.6 microM). Using cryopreserved cells from study days 0, 3, 7, 14, and 30, thawed and tested simultaneously, there was no significant difference at the p less than or equal to 0.05 level between the net proliferative responses at each time point for the two groups. On day 14, however, the proliferative response of the acyclovir group was approximately 50% lower than that of the placebo group. Geometric mean antibody titer rises to varicella-zoster virus were also lower among drug recipients but not significantly so. Although this dose of acyclovir did not have a statistically significant effect on lymphocyte proliferative responses to varicella-zoster virus antigen or antibody titers, the lower values in drug recipients may be a reflection of the ability of acyclovir to terminate viral replication, thus reducing the patient's antigenic burden.

摘要

在一项针对免疫功能正常患者的口服阿昔洛韦治疗急性带状疱疹的安慰剂对照试验中,我们检测了安慰剂组和阿昔洛韦组患者外周血单个核细胞的增殖反应及抗体滴度,以确定该药物是否影响细胞介导免疫反应或体液免疫反应。当新鲜外周血单个核细胞在口服阿昔洛韦(每日2 g,疗程10天,血浆药物水平平均为4.6 microM)前及治疗第7天采集的自体血清中同时进行检测时,对有丝分裂原和两种稀释度水痘 - 带状疱疹病毒抗原的增殖反应未受抑制。使用研究第0、3、7、14和30天冻存的细胞,解冻后同时进行检测,两组在每个时间点的净增殖反应在p≤0.05水平上无显著差异。然而,在第14天,阿昔洛韦组的增殖反应比安慰剂组低约50%。药物治疗组患者对水痘 - 带状疱疹病毒的几何平均抗体滴度升高也较低,但无显著差异。虽然该剂量的阿昔洛韦对淋巴细胞对水痘 - 带状疱疹病毒抗原的增殖反应或抗体滴度没有统计学上的显著影响,但药物治疗组较低的值可能反映了阿昔洛韦终止病毒复制的能力,从而减轻了患者的抗原负担。

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