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HIV 相关进展性多灶性白质脑病中免疫重建炎症综合征的发病率和预后

Incidence and prognosis of immune reconstitution inflammatory syndrome in HIV-associated progressive multifocal leucoencephalopathy.

作者信息

Sainz-de-la-Maza S, Casado J L, Pérez-Elías M J, Moreno A, Quereda C, Moreno S, Corral I

机构信息

Department of Neurology, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Department of Infectious Diseases, Hospital Universitario Ramón y Cajal, Madrid, Spain.

出版信息

Eur J Neurol. 2016 May;23(5):919-25. doi: 10.1111/ene.12963. Epub 2016 Feb 23.

Abstract

BACKGROUND AND PURPOSE

Progressive multifocal leucoencephalopathy-associated immune reconstitution inflammatory syndrome (PML-IRIS) is the paradoxical worsening or unmasking of preexisting infection with JC virus attributable to a rapid recovery of the immune system after highly active antiretroviral therapy (HAART) initiation. We investigated the incidence and factors associated with PML-IRIS in HIV-infected patients. We also studied its influence on mortality of PML and the effect of corticosteroid therapy.

METHODS

Single-center retrospective analysis of HIV-infected patients diagnosed with PML from 1996 to 2012 who received HAART.

RESULTS

Among 59 PML patients treated with HAART, 18 (30.51%) developed PML-IRIS (five delayed PML-IRIS, 13 simultaneous PML-IRIS). Patients who developed IRIS had lower CD4 counts prior to treatment (102 vs. 68.5, P < 0.05) and experienced a greater decline in HIV-RNA levels in response to HAART (2.5log vs. 2.95log, P < 0.05). Gadolinium enhancement on MRI was observed in 31.25% of PML-IRIS cases versus 2.56% of PML non-IRIS (P < 0.01). Survival rates were higher in patients with PML-IRIS compared to those with PML non-IRIS. Eight patients received corticosteroids, five of which had a good outcome. Patients who died were severely ill when treatment was initiated whereas patients who survived were treated before major neurological deterioration occurred.

CONCLUSIONS

Nearly one-third of HIV-infected patients with PML develop IRIS after initiating HAART. Patients severely immunocompromised who experience a rapid virological response to HAART have a higher risk for PML-IRIS. There was a trend for lower mortality in patients with IRIS. Early treatment with corticosteroids might be useful.

摘要

背景与目的

进行性多灶性白质脑病相关免疫重建炎症综合征(PML-IRIS)是指在高效抗逆转录病毒治疗(HAART)开始后,免疫系统迅速恢复导致的既往JC病毒感染的矛盾性恶化或暴露。我们调查了HIV感染患者中PML-IRIS的发生率及相关因素。我们还研究了其对PML死亡率的影响以及皮质类固醇治疗的效果。

方法

对1996年至2012年期间接受HAART治疗且诊断为PML的HIV感染患者进行单中心回顾性分析。

结果

在59例接受HAART治疗的PML患者中,18例(30.51%)发生了PML-IRIS(5例为延迟性PML-IRIS,13例为同时性PML-IRIS)。发生IRIS的患者治疗前CD4细胞计数较低(102对68.5,P<0.05),且对HAART的反应中HIV-RNA水平下降幅度更大(2.5log对2.95log,P<0.05)。MRI上钆增强在31.25%的PML-IRIS病例中可见,而在非IRIS的PML病例中为2.56%(P<0.01)。与非IRIS的PML患者相比,PML-IRIS患者的生存率更高。8例患者接受了皮质类固醇治疗,其中5例预后良好。死亡患者在开始治疗时病情严重,而存活患者在主要神经功能恶化发生前接受了治疗。

结论

近三分之一的HIV感染PML患者在开始HAART后发生IRIS。免疫严重受损且对HAART有快速病毒学反应的患者发生PML-IRIS的风险更高。IRIS患者的死亡率有降低趋势。早期使用皮质类固醇治疗可能有用。

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