Enrichment of activated monocytes in cerebrospinal fluid during antiretroviral therapy

被引:15
作者
Neuenburg, JK
Furlan, S
Bacchetti, P
Price, RW
Grant, RM
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
关键词
D O I
10.1097/01.aids.0000181008.39514.ee
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: In HIV infection, activated monocytes are enriched in blood and in the perivascular area of the brain, especially in patients with HIV-associated dementia. Although clinical brain disease is uncommon during combination antiretroviral therapy (ART), autopsy series indicate that HIV-infected brain tissue can contain high numbers of monocytes/macrophages despite ART. Design: We assessed activated monocytes in blood and cerebrospinal fluid (CSF) in 76 living patients on and off ART. Plasma lipids were measured because they have been associated with monocyte activation and ART. Methods: A novel quantitative six-color flow cytometric approach was used to identify monocytes in blood and CSF and to evaluate monocyte activation status. Results: The mean percentage and number of activated CD16 monocytes in CSF was highest in individuals on combination ART, especially in those receiving protease inhibitors (PI). CSF viral load was also associated with higher monocyte activation in CSF. The mean calculated low density lipoprotein (LDL)-, oxidized LDL- and total cholesterol in plasma were highest in patients receiving PI. Conclusions: Activated monocytes are enriched in the CSF of persons living with HIV-1 and receiving ART. This finding is consistent with previously reported autopsy series. The mechanisms and long-term clinical consequences of persistent monocyte activation require further study. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1351 / 1359
页数:9
相关论文
共 60 条
[11]   Chemokines in the pathogenesis of vascular disease [J].
Charo, IF ;
Taubman, MB .
CIRCULATION RESEARCH, 2004, 95 (09) :858-866
[12]   Chemokine receptor 2 (CCR2) in atherosclerosis, infectious diseases, and regulation of T-cell polarization [J].
Charo, IF ;
Peters, W .
MICROCIRCULATION, 2003, 10 (3-4) :259-264
[13]   HIV-1 expression protects macrophages and microglia from apoptotic death [J].
Cosenza, MA ;
Zhao, ML ;
Lee, SC .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2004, 30 (05) :478-490
[14]   Epidemiology of HIV cardiac disease [J].
Cotter, BR .
PROGRESS IN CARDIOVASCULAR DISEASES, 2003, 45 (04) :319-326
[15]   Marked improvement in survival following AIDS dementia complex in the era of highly active antiretroviral therapy [J].
Dore, GJ ;
McDonald, A ;
Li, YM ;
Kaldor, JM ;
Brew, BJ .
AIDS, 2003, 17 (10) :1539-1545
[16]   HIV protease inhibitors promote atherosclerotic lesion formation independent of dyslipidemia by increasing CD36-dependent cholesteryl ester accumulation in macrophages [J].
Dressman, J ;
Kincer, J ;
Matveev, SV ;
Guo, L ;
Greenberg, RN ;
Guerin, T ;
Meade, D ;
Li, XA ;
Zhu, WF ;
Uittenbogaard, A ;
Wilson, ME ;
Smart, EJ .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (03) :389-397
[17]   Ischaemic cerebrovascular events in HIV infection - A cohort study [J].
Evers, S ;
Nabavi, D ;
Rahmann, A ;
Heese, C ;
Reichelt, D ;
Husstedt, IW .
CEREBROVASCULAR DISEASES, 2003, 15 (03) :199-205
[18]  
Fantoni Massimo, 2002, Ital Heart J, V3, P294
[19]   Targeted disruption of the class B scavenger receptor CD36 protects against atherosclerotic lesion development in mice [J].
Febbraio, M ;
Podrez, EA ;
Smith, JD ;
Hajjar, DP ;
Hazen, SL ;
Hoff, HF ;
Sharma, K ;
Silverstein, RL .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (08) :1049-1056
[20]   CNS invasion by CD14+/CD16+peripheral blood-derived monocytes in HIV dementia:: perivascular accumulation and reservoir of HIV infection [J].
Fischer-Smith, T ;
Croul, S ;
Sverstiuk, AE ;
Capini, C ;
L'Heureux, D ;
Régulier, EG ;
Richardson, MW ;
Amini, S ;
Morgello, S ;
Khalili, K ;
Rappaport, J .
JOURNAL OF NEUROVIROLOGY, 2001, 7 (06) :528-541