Asymptomatic Cerebrospinal Fluid HIV-1 Escape: Incidence and Consequences

被引:0
作者
Ulfhammer, Gustaf [1 ,2 ]
Yilmaz, Aylin [1 ,2 ]
Mellgren, Asa [1 ,2 ]
Tyrberg, Erika [1 ,2 ]
Sorstedt, Erik [1 ,2 ]
Hagberg, Lars [1 ,2 ]
Gostner, Johanna [3 ]
Fuchs, Dietmar [4 ]
Zetterberg, Henrik [5 ,6 ,7 ,8 ,9 ,10 ]
Nilsson, Staffan [11 ]
Nystrom, Kristina [1 ,2 ]
Eden, Arvid [1 ,2 ]
Gisslen, Magnus [1 ,2 ,12 ]
机构
[1] Univ Gothenburg, Inst Biomed, Sahlgrenska Acad, Dept Infect Dis, Medicinaregatan 3, S-40530 Gothenburg, Sweden
[2] Sahlgrens Univ Hosp, Dept Infect Dis, Gothenburg, Sweden
[3] Innsbruck Med Univ, Inst Med Biochem, Bioctr, Innsbruck, Austria
[4] Innsbruck Med Univ, Inst Biol Chem, Bioctr, Innsbruck, Austria
[5] Univ Gothenburg, Inst Neurosci & Physiol, Sahlgrenska Acad, Dept Psychiat & Neurochem, Gothenburg, Sweden
[6] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[7] UCL, Inst Neurol, Dept Neurodegenerat Dis, London, England
[8] UCL, UK Dementia Res Inst, London, England
[9] Hong Kong Ctr Neurodegenerat Dis, Hong Kong, Peoples R China
[10] Univ Wisconsin Madison, Wisconsin Alzheimers Dis Res Ctr, Sch Med & Publ Hlth, Madison, WI USA
[11] Univ Gothenburg, Inst Biomed, Sahlgrenska Acad, Dept Lab Med, Gothenburg, Sweden
[12] Publ Hlth Agcy Sweden, Solna, Sweden
基金
瑞典研究理事会;
关键词
HIV-1; neopterin; immune activation; albumin ratio; neurofilament protein light; ANTIRETROVIRAL THERAPY; VIRAL ESCAPE; HIV-1-INFECTED PATIENTS; IMMUNE ACTIVATION; NEURONAL INJURY; RNA ESCAPE; DISCORDANCE; SYMPTOMS;
D O I
10.1093/infdis/jiae555
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The incidence and clinical relevance of asymptomatic cerebrospinal fluid escape (CSFE) during antiretroviral therapy (ART) is uncertain. We examined the impact and incidence of asymptomatic CSFE in a Swedish HIV cohort. Methods. Neuroasymptomatic people with HIV (PWH) who have been on ART for at least 6 months with suppressed plasma viral load were followed longitudinally. CSFE was defined as either increased CSF HIV-1 RNA with concurrent plasma suppression or CSF HIV-1 RNA exceeding that in plasma when both were quantifiable. Paired CSF and plasma were analyzed for HIV-1 RNA, neopterin, neurofilament light protein (NfL), white blood cell (WBC) count, and albumin ratio. Results. Asymptomatic CSFE (cutoff 50 copies/mL) was found in 4 of 173 PWH (2%) and 5 of 449 samples (1%). The corresponding proportions were 8% of PWH and 4% for samples using a 20 copies/mL cutoff for CSF HIV-1 RNA. CSFE samples (cutoff 20 copies/mL) had a 25% higher geometric mean of CSF neopterin (P = .01) and 8% higher albumin ratio (P = .04) compared to samples without CSFE. No differences were observed in CSF NfL levels (P = .8). The odds ratio for increased CSF WBC (>= 3 cells/mu L) in samples with CSFE was 3.9 (P = .004), compared to samples without elevated CSF viral load. Conclusions. Asymptomatic CSFE was identified in only 4 (2%) PWH, with no cases of continuous CSFE observed. Increased CSF HIV-1 RNA was associated with biomarkers of CNS immune activation and blood-brain barrier impairment, but not with biomarkers of neuronal injury.
引用
收藏
页码:e429 / e437
页数:9
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