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首页> 外文期刊>Clinical & developmental immunology. >Coinfection by Hepatitis C Is Strongly Associated with Abnormal CD4/CD8 Ratio in HIV Patients under Stable ART in Salvador, Brazil
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Coinfection by Hepatitis C Is Strongly Associated with Abnormal CD4/CD8 Ratio in HIV Patients under Stable ART in Salvador, Brazil

机译:在稳定的ART下,巴西萨尔瓦多的丙型肝炎合并感染与CD4 / CD8比率异常有关。

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摘要

Proper immune restoration (CD4 count >500 and normal CD4/8 ratio) is reached only by a fraction of HIV patients, despite stable viral suppression. Methods. We present a case-control study to compare HIV patients with viral suppression >1 year, according to immune restoration pattern: adequate response (AR) denned by CD4 > 500 cells/mm3 and CD4/8 ratio >1; partial response (PR = patients with CD4 > 500, but CD4/8 ratio <1); inadequate response (IR = CD4 < 500 cells). Results. We evaluated 293 consecutive patients (89 AR, 112 PR, and 92 IR), 70% males. Male gender (p < 0.01), lower mean CD4 nadir (p < 0.001), higher baseline VL {p = 0.01), previous diagnosis of Tb (p = 0.03), or HCV {p < 0.01) was associated with IR. Likelihood of AR/PR was similar regardless of gender, after adjusting for nadir CD4+ cells count. Longer time under suppressive ART was also associated with a greater chance of AR, but logistic regression identified coinfection by HCV as the main factor associated with abnormal CD4/CD8 ratio. Conclusion. Early initiation of ART and longer time since first undetectable PVL were predictors of AR. Previous HCV diagnosis significantly increases the risk of abnormal CD4/CD8 ratio.
机译:尽管有稳定的病毒抑制作用,但只有一小部分HIV患者可以实现适当的免疫恢复(CD4计数> 500,CD4 / 8比率正常)。方法。我们提供了一项病例对照研究,根据免疫恢复模式比较病毒抑制> 1年的HIV患者:CD4> 500细胞/ mm3和CD4 / 8比> 1所确定的充分反应(AR);部分反应(PR = CD4> 500但CD4 / 8比率<1的患者);反应不足(IR = CD4 <500个细胞)。结果。我们评估了293例连续患者(89例AR,112例PR和92例IR),其中70%为男性。男性(p <0.01),平均CD4最低点(p <0.001),基线VL(p = 0.01)较高,先前诊断为Tb(p = 0.03)或HCV(p <0.01)与IR相关。调整最低点CD4 +细胞计数后,不论性别,AR / PR的可能性均相似。抑制性抗逆转录病毒治疗时间越长,发生AR的机会也越大,但逻辑回归分析表明HCV合并感染是与异常CD4 / CD8比值相关的主要因素。结论。自从首次发现PVL以来,ART的提早开始和更长的时间是AR的预测指标。先前的HCV诊断显着增加了CD4 / CD8比值异常的风险。

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