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Plasma Levels of Neopterin and C-Reactive Protein (CRP) in Tuberculosis (TB) with and without HIV Coinfection in Relation to CD4 Cell Count

机译:伴或不伴有HIV合并感染的结核病(TB)中新蝶呤和C反应蛋白(CRP)的血浆水平与CD4细胞计数有关

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摘要

Background While the risk of TB is elevated in HIV-positive subjects with low CD4 cell counts, TB may in itself be associated with CD4 lymphocytopenia. We investigated markers of immune activation (neopterin) and inflammation (CRP) in TB patients with and without HIV coinfection and their association with CD4 cell levels, and determined their predictive capacity as alternative markers of advanced immunosuppression. Methods Participants selected from a cohort of adults with TB at Ethiopian health centers (195 HIV +/TB+, 170 HIV-/TB+) and 31 controls were tested for plasma levels of neopterin and CRP. Baseline levels of neopterin and CRP were correlated to CD4 cell count before and after anti-TB treatment (ATT). The performance to predict CD4 cell strata for both markers were investigated using receiver operating curves. Results Levels of both biomarkers were elevated in TB patients (neopterin: HIV+/TB+ 54 nmol/l, HIV-/TB+ 23 nmol/l, controls 3.8 nmol/l; CRP: HIV+/TB+ 36 mu g/ml, HIV-/TB+ 33 mu g/ml, controls 0.5 mu g/ml). Neopterin levels were inversely correlated (-0.53, p<0.001) to CD4 cell count, whereas this correlation was weaker for CRP (-0.25, p<0.001). Neither of the markers had adequate predictive value for identification of subjects with CD4 cell count <100 cells/mm(3) (area under the curve [AUC] 0.64 for neopterin, AUC 0.59 for CRP). Conclusion Neopterin levels were high in adults with TB, both with and without HIV coinfection, with inverse correlation to CD4 cell count. This suggests that immune activation may be involved in TB-related CD4 lymphocytopenia. However, neither neopterin nor CRP showed promise as alternative tests for immunosuppression in patients coinfected with HIV and TB.
机译:背景技术虽然CD4细胞计数低的HIV阳性受试者的结核病风险增加,但结核病本身可能与CD4淋巴细胞减少有关。我们调查了有或没有HIV合并感染的结核病患者的免疫激活(新蝶呤)和炎症(CRP)标志物,以及它们与CD4细胞水平的关系,并确定了其作为晚期免疫抑制替代标志物的预测能力。方法对来自埃塞俄比亚卫生中心成年结核病人群(195 HIV + / TB +,170 HIV- / TB +)和31名对照组的参与者进行血浆新蝶呤和CRP水平的检测。新蝶呤和CRP的基线水平与抗TB治疗(ATT)之前和之后的CD4细胞计数相关。使用接收器操作曲线研究了预测两种标记的CD4细胞分层的性能。结果TB患者的两种生物标志物水平均升高(新opter呤:HIV + / TB + 54 nmol / l,HIV- / TB + 23 nmol / l,对照3.8 nmol / l; CRP:HIV + / TB + 36μg / ml,HIV- / TB + 33微克/毫升,对照0.5微克/毫升)。新蝶呤水平与CD4细胞计数呈负相关(-0.53,p <0.001),而对于CRP,这种相关性较弱(-0.25,p <0.001)。这两种标记物都没有足够的预测值来鉴定CD4细胞计数<100细胞/ mm(3)的受试者(新蝶呤的曲线下面积[AUC]为0.64,CRP的面积为AUC 0.59)。结论合并和不合并HIV合并感染的结核病成人新蝶呤水平均较高,与CD4细胞计数呈负相关。这表明免疫激活可能与TB相关的CD4淋巴细胞减少有关。但是,新蝶呤和CRP均未显示出有望作为合并感染HIV和TB的患者进行免疫抑制的替代测试。

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