Plasma levels of soluble CD14 and tumor necrosis factor-α type II receptor correlate with cognitive dysfunction during human immunodeficiency virus type 1 infection

被引:73
作者
Ryan, LA
Zheng, JL
Brester, M
Bohac, D
Hahn, F
Anderson, J
Ratanasuwan, W
Gendelman, HE
Swindells, S
机构
[1] Univ Nebraska, Med Ctr, Ctr Neurovirol & Neurodegenerat Disorder, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Dept Pathol & Microbiol, Omaha, NE USA
[3] Univ Nebraska, Med Ctr, Dept Internal Med, Omaha, NE USA
[4] Univ Nebraska, Med Ctr, Dept Psychiat, Omaha, NE USA
[5] Univ Nebraska, Med Ctr, Dept Radiol, Omaha, NE 68105 USA
[6] Univ Nebraska, Med Ctr, Dept Prevent & Social Med, Omaha, NE USA
关键词
D O I
10.1086/323036
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The relationship between monocyte immune responses and cognitive impairment during progressive human immunodeficiency virus type 1 (HIV-1) infection was investigated in 28 subjects receiving highly active antiretroviral therapy. The mean +/- SEM CD4(+) T lymphocyte count and virus load for all patients were 237 +/- 41 cells/mm(3) and 77,091 +/- 195,372 HIV-1 RNA copies/mL, respectively. Levels of soluble tumor necrosis factor-alpha type II receptor (sTNF-RII) and soluble CD14 (sCD14) were measured in plasma by ELISA and were correlated with results from neuropsychological, magnetic resonance imaging, and magnetic resonance spectroscopy tests. Plasma sCD14 and sTNF-RII levels were elevated in subjects with cognitive impairment and in those with brain atrophy. Furthermore, both factors were correlated with spectroscopic choline: creatine ratios. These findings support the idea that peripheral immune responses are linked to cognitive dysfunction during advanced HIV-1 disease.
引用
收藏
页码:699 / 706
页数:8
相关论文
共 65 条
[1]   STABILIZATION OF THE BIOACTIVITY OF TUMOR-NECROSIS-FACTOR BY ITS SOLUBLE RECEPTORS [J].
ADERKA, D ;
ENGELMANN, H ;
MAOR, Y ;
BRAKEBUSCH, C ;
WALLACH, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (02) :323-329
[2]   Impact of highly active anti-retroviral therapy (HAART) on cytokine production and monocyte subsets in HIV-infected patients [J].
Amirayan-Chevillard, N ;
Tissot-Dupont, H ;
Capo, C ;
Brunet, C ;
Dignat-George, F ;
Obadia, Y ;
Gallais, H ;
Mege, JL .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2000, 120 (01) :107-112
[3]  
AUKRUST P, 1994, J INFECT DIS, V169, P1186
[4]  
BAZIL V, 1991, J IMMUNOL, V147, P1567
[5]  
BONNET F, 2001, 8 C RETR OPP INF CHI, P62
[6]   Antiretroviral therapy in adults - Updated recommendations of the International AIDS Society-USA Panel [J].
Carpenter, CCJ ;
Cooper, DA ;
Fischl, MA ;
Gatell, JM ;
Gazzard, BG ;
Hammer, SM ;
Hirsch, MS ;
Jacobsen, DM ;
Katzenstein, DA ;
Montaner, JSG ;
Richman, DD ;
Saag, MS ;
Schechter, M ;
Schooley, RT ;
Vella, S ;
Yeni, PG ;
Volberding, PA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (03) :381-390
[7]   Highly active antiretroviral therapy reverses brain metabolite abnormalities in mild HIV dementia [J].
Chang, L ;
Ernst, T ;
Leonido-Yee, M ;
Witt, M ;
Speck, O ;
Walot, I ;
Miller, EN .
NEUROLOGY, 1999, 53 (04) :782-789
[8]   PROTON SPECTROSCOPY OF THE BRAIN IN HIV-INFECTION - CORRELATION WITH CLINICAL, IMMUNOLOGICAL, AND MR-IMAGING FINDINGS [J].
CHONG, WK ;
SWEENEY, B ;
WILKINSON, ID ;
PALEY, M ;
HALLCRAGGS, MA ;
KENDALL, BE ;
SHEPARD, JK ;
BEECHAM, M ;
MILLER, RF ;
WELLER, IVD ;
NEWMAN, SP ;
HARRISON, MJG .
RADIOLOGY, 1993, 188 (01) :119-124
[9]   Human immunodeficiency virus-associated dementia [J].
Clifford, DB .
ARCHIVES OF NEUROLOGY, 2000, 57 (03) :321-324
[10]   A mechanism of TNFR type II (75 kDa) "shedding" in macrophages [J].
Coyne, CP ;
Willetto, C ;
Fenwick, BW .
SHOCK, 1999, 11 (01) :19-28