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
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