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Serious Non-AIDS Events: Therapeutic Targets of Immune Activation and Chronic Inflammation in HIV Infection

机译:严重的非艾滋病事件:HIV感染中免疫活化和慢性炎症的治疗目标

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摘要

In the antiretroviral therapy (ART) era, serious non-AIDS events (SNAEs) have become the major causes of morbidity and mortality in HIV-infected persons. Early ART initiation has the strongest evidence for reducing SNAEs and mortality. Biomarkers of immune activation, inflammation and coagulopathy do not fully normalize despite virologic suppression and persistent immune activation is an important contributor to SNAEs. A number of strategies aimed to reduce persistent immune activation including ART intensification to reduce residual viremia; treatment of co-infections to reduce chronic antigen stimulation; the use of anti-inflammatory agents, reducing microbial translocation as well as interventions to improve immune recovery through cytokine administration and reducing lymphoid tissue fibrosis, have been investigated. To date, there is little conclusive evidence on which strategies beyond treatment of hepatitis B and C co-infections and reducing cardiovascular risk factors will result in clinical benefits in patients already on ART with viral suppression. The use of statins seems to show early promise and larger clinical trials are underway to confirm their efficacy. At this stage, clinical care of HIV-infected patients should therefore focus on early diagnosis and prompt ART initiation, treatment of active co-infections and the aggressive management of co-morbidities until further data are available.
机译:在抗逆转录病毒疗法(ART)时代,严重的非艾滋病事件(SNAE)已成为HIV感染者发病和死亡的主要原因。尽早开展抗逆转录病毒疗法具有降低SNAE和死亡率的最有力证据。尽管有病毒学抑制作用,但免疫激活,炎症和凝血病的生物标志物并未完全正常化,持续的免疫激活是SNAE的重要因素。旨在减少持续性免疫活化的许多策略包括加强抗病毒治疗以减少残留病毒血症;治疗合并感染以减少慢性抗原刺激;已经研究了使用抗炎药,减少微生物易位以及通过施用细胞因子和减少淋巴样组织纤维化来改善免疫恢复的干预措施。迄今为止,几乎没有确凿的证据表明,除了治疗乙型和丙型肝炎合并感染以及降低心血管危险因素以外,哪些策略将对已经接受病毒抑制的抗逆转录病毒疗法的患者带来临床益处。他汀类药物的使用似乎显示出早期的希望,正在进行更大的临床试验以证实其功效。因此,在此阶段,HIV感染患者的临床护理应着重于早期诊断和迅速的抗病毒治疗,活动性合并感染的治疗以及对合并症的积极管理,直到获得更多数据为止。

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