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基线CD4细胞计数对病毒学抑制个体抗逆转录病毒治疗短期免疫反应临床意义的影响。

Effect of baseline CD4 cell counts on the clinical significance of short-term immunologic response to antiretroviral therapy in individuals with virologic suppression.

作者信息

Moore David M, Harris Ross, Lima Viviane, Hogg Bob, May Margaret, Yip Benita, Justice Amy, Mocroft Amanda, Reiss Peter, Lampe Fiona, Chêne Geneviève, Costagliola Dominique, Elzi Luigia, Mugavero Michael J, Monforte Antonella D'Arminio, Sabin Caroline, Podzamczer Daniel, Fätkenheuer Gerd, Staszewski Schlomo, Gill John, Sterne Jonathan A C

机构信息

Division of Epidemiology and Population Health, British Columbia Centre for Excellence in HIV/AIDS, Vancouver, Canada.

出版信息

J Acquir Immune Defic Syndr. 2009 Nov 1;52(3):357-63. doi: 10.1097/QAI.0b013e3181b62933.

Abstract

BACKGROUND

Achieving virologic suppression is a clear therapeutic goal for patients receiving combination antiretroviral therapy (cART). However, the effects of immunologic responses, whether measured as CD4 count changes from baseline or CD4 counts at follow-up, in patients with virologic suppression, have not been clearly established.

METHODS

Treatment-naive individuals aged > or =16 years, who initiated cART between 1998 and 2005 in participating cohorts of the ART Cohort Collaboration and achieved viral load < or =400 copies per milliliter 6 months after cART initiation, were included. We used Cox models to examine associations of CD4 change from baseline to 6 months, and absolute CD4 counts at 6 months, with subsequent rates of mortality and AIDS. Analyses were stratified by baseline CD4 count.

RESULTS

Among 23,679 eligible participants, the median increase in CD4 count at 6 months, and the implications of these increases for subsequent mortality and AIDS, varied with baseline CD4 count. Mortality hazard ratios for increases of 0-50 cells per microliter, compared with >100 cells per microliter, were 1.87 (95% confidence interval: 1.28 to 2.73), 1.60 (1.13 to 2.28), 0.98 (0.58 to 1.65) and 1.24 (0.70 to 2.18) in participants with baseline CD4 cell count <50, 50-199, 200-349 and > or =350 cells per microliter, respectively. In contrast, hazard ratios for mortality or AIDS associated with absolute CD4 cell counts at 6 months were similar across all but the highest baseline CD4 cell count strata.

CONCLUSION

It is not possible to derive thresholds for change in CD4 count that define an adequate immunologic response in individuals receiving cART. Absolute CD4 counts at 6 months are a more useful measure of immunologic response and subsequent prognosis.

摘要

背景

实现病毒学抑制是接受联合抗逆转录病毒治疗(cART)患者的明确治疗目标。然而,在病毒学抑制的患者中,免疫反应的影响,无论是以CD4细胞计数相对于基线的变化还是随访时的CD4细胞计数来衡量,都尚未明确确立。

方法

纳入1998年至2005年间在抗逆转录病毒治疗队列协作研究的参与队列中开始接受cART治疗、年龄≥16岁且在开始cART治疗6个月后病毒载量≤400拷贝/毫升的初治个体。我们使用Cox模型来检验从基线到6个月时CD4细胞计数的变化以及6个月时的绝对CD4细胞计数与随后的死亡率和艾滋病发病率之间的关联。分析按基线CD4细胞计数进行分层。

结果

在23679名符合条件的参与者中,6个月时CD4细胞计数的中位数增加情况以及这些增加对随后死亡率和艾滋病的影响因基线CD4细胞计数而异。与每微升增加>100个细胞相比,每微升增加0 - 50个细胞时的死亡风险比在基线CD4细胞计数<50、50 - 199、200 - 349和≥350个细胞/微升的参与者中分别为1.87(95%置信区间:1.28至2.73)、1.60(1.13至2.28)、0.98(0.58至1.65)和1.24(0.70至2.18)。相比之下,除了最高基线CD4细胞计数分层外,6个月时与绝对CD4细胞计数相关的死亡或艾滋病风险比在所有分层中相似。

结论

对于接受cART治疗的个体,无法得出定义充分免疫反应的CD4细胞计数变化阈值。6个月时的绝对CD4细胞计数是免疫反应及随后预后的更有用衡量指标。

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