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当代人类免疫缺陷病毒患者队列中鸟分枝杆菌复合群免疫重建炎症综合征的临床和免疫学预测因素

Clinical and Immunologic Predictors of Mycobacterium avium Complex Immune Reconstitution Inflammatory Syndrome in a Contemporary Cohort of Patients With Human Immunodeficiency Virus.

作者信息

Breglio Kimberly F, Vinhaes Caian L, Arriaga María B, Nason Martha, Roby Gregg, Adelsberger Joseph, Andrade Bruno B, Sheikh Virginia, Sereti Irini

机构信息

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Bahia, Brazil.

出版信息

J Infect Dis. 2021 Jun 15;223(12):2124-2135. doi: 10.1093/infdis/jiaa669.

Abstract

BACKGROUND

People with human immunodeficiency virus (HIV) can present with new or worsening symptoms associated with Mycobacterium avium complex (MAC) infection shortly after antiretroviral therapy (ART) initiation as MAC immune reconstitution inflammatory syndrome (MAC-IRIS). In this study, we assessed the utility of several laboratory tests as predictors of MAC-IRIS.

METHODS

People with HIV with clinical and histologic and/or microbiologic evidence of MAC-IRIS were identified and followed up to 96 weeks post-ART initiation within a prospective study of 206 ART-naive patients with CD4 <100 cells/µL.

RESULTS

Fifteen (7.3%) patients presented with MAC-IRIS within a median interval of 26 days after ART initiation. Patients who developed MAC-IRIS had lower body mass index, lower hemoglobin levels, higher alkaline phosphatase (ALP), and increased CD38 frequency and mean fluorescence intensity on CD8+ T cells at the time of ART initiation compared with non-MAC IRIS patients. A decision tree inference model revealed that stratifying patients based on levels of ALP and D-dimer could predict the likelihood of MAC-IRIS. A binary logistic regression demonstrated that higher levels of ALP at baseline were associated with increased risk of MAC-IRIS development.

CONCLUSIONS

High ALP levels and increased CD8+ T-cell activation with low CD4 counts at ART initiation should warrant suspicion for subsequent development of MAC-IRIS.

摘要

背景

感染人类免疫缺陷病毒(HIV)的患者在开始抗逆转录病毒治疗(ART)后不久,可能会出现与鸟分枝杆菌复合体(MAC)感染相关的新症状或症状加重,即MAC免疫重建炎症综合征(MAC-IRIS)。在本研究中,我们评估了几种实验室检查作为MAC-IRIS预测指标的效用。

方法

在一项对206例未接受过ART治疗、CD4细胞计数<100个/µL的患者进行的前瞻性研究中,识别出有临床、组织学和/或微生物学证据表明患有MAC-IRIS的HIV患者,并在ART开始后随访至96周。

结果

15例(7.3%)患者在ART开始后的中位间隔26天内出现MAC-IRIS。与未发生MAC-IRIS的患者相比,发生MAC-IRIS的患者在ART开始时体重指数较低、血红蛋白水平较低(低体重指数、低血红蛋白水平、高碱性磷酸酶(ALP)),且CD8+T细胞上的CD38频率和平均荧光强度增加。决策树推理模型显示,根据ALP和D-二聚体水平对患者进行分层可以预测MAC-IRIS的可能性。二元逻辑回归表明,基线时较高的ALP水平与MAC-IRIS发生风险增加相关。

结论

ART开始时ALP水平升高以及CD4计数低时CD8+T细胞活化增加应引起对随后发生MAC-IRIS的怀疑。

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