In vivo demonstration of neuroinflammatory molecule expression in brain abscess with diffusion tensor imaging

American Journal of Neuroradiology

Volumn 29, Issue 2, 2008, Pages 326-332

  Gupta, Rakesh K ^a   Nath, K ^a   Prasad, A ^a   Prasad, K N ^a   Husain, M ^b   Rathore, R K S ^c   Husain, N ^b   Srivastava, C ^b   Khetan, P ^b   Trivedi, R ^a   Narayana, P A ^d  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

^b KING GEORGE'S MEDICAL UNIVERSITY   (India)

^c INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

^d UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GADODIAMIDE; INTERCELLULAR ADHESION MOLECULE 1; INTERLEUKIN 1BETA; LYMPHOCYTE FUNCTION ASSOCIATED ANTIGEN 1; TUMOR NECROSIS FACTOR ALPHA;

ADOLESCENT; ADULT; ANISOTROPY; ARTICLE; BRAIN ABSCESS; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DIFFUSION TENSOR IMAGING; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; HUMAN; HUMAN CELL; IN VIVO STUDY; INFLAMMATION; LEUKEMIA CELL LINE; MALE; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; STAPHYLOCOCCUS AUREUS; STATISTICAL ANALYSIS;

ADOLESCENT; ADULT; BIOLOGICAL MARKERS; BRAIN ABSCESS; CHILD; CHILD, PRESCHOOL; CYTOKINES; DIFFUSION MAGNETIC RESONANCE IMAGING; FEMALE; FORECASTING; HUMANS; INFANT; JURKAT CELLS; MALE; MIDDLE AGED; MOLECULAR PROBE TECHNIQUES;

EID: 39649117152     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: 10.3174/ajnr.A0826     Document Type: Article

References (33)

1. Mathisen GE, Johnson JP. Brain abscess. Clin Infect Dis 1997;25:763-92
2. Townsend GC, Scheid WM. Infections of the central nervous system. Adv Internal Med 1998;43:403-47
3. Kielian T. Immunopathogenesis of brain abscess. J Neuroinflammation 2004;17:1-16
4. Kielian T. Microglia and chemokines in infectious diseases of the nervous system: views and reviews. Front Biosci 2004;9:732-50
5. Kielian T, Bearden ED, Baldwin AC. IL-1 and TNF-alpha play a pivotal role in the host immune response in a mouse model of Staphylococcus aureus-induced experimental brain abscess. J Neuropathol Exp Neurol 2004;63:381-96
6. Wong D, Dorovini-Zis K. Upregulation of intercellular adhesion molecule-1 (ICAM-1) expression in primary cultures of human brain microvessel endothelial cells by cytokines and lipopolysaccharide. J Neuroimmunol 1992;39:11-21
7. Vassalli P. The pathophysiology of tumor necrosis factors. Annu Rev Immunol 1992;10:411-528
8. Bevilacqua MP. Endothelial-leukocyte adhesion molecules. Annu Rev Immunol 1993;11:767-804
9. Mori S, Zhang J. Principles of diffusion tensor imaging and its application to basic neuroscience research. Neuron 2006;51:527-39
10. Gupta RK, Hasan KM, Mishra AM, et al. High fractional anisotropy in brain abscesses versus other cystic intracranial lesions. AJNR Am J Neuroradiol 2005;26:1107-14
11. Prasad KN, Mishra AM, Gupta D, et al. Analysis of microbial etiology and mortality in patients with brain abscess. J Infect 2006;53:221-27
12. Basser PJ. Inferring microstructural features and the physiological state of tissues from diffusion-weighted images. NMR Biomed 1995;8:333-44
13. Hasan KM, Parker DL, Alexander AL. Comparison of gradient encoding schemes for diffusion-tensor MRI. J Magn Reson Imaging 2001;13:769-80
14. Batchelor PG, Atkinson D, Hill DL, et al. Anisotropic noise propagation in diffusion tensor MRI sampling schemes. Magn Reson Med 2003;49:1143-51
15. Hasan KM, Narayana PA. Computation of the fractional anisotropy and mean diffusivity maps without tensor decoding and diagonalization: theoretical analysis and validation. Magn Reson Med 2003;50:589-98
16. Zhang Z, van den Bos EJ, Wielopolski PA, et al. High-resolution magnetic resonance imaging of iron-labeled myoblasts using a standard 1.5-T clinical scanner. MAGMA 2004;17:201-09
17. Segura M, Stankova J, Gottschalk M. Heat-killed Streptococcus suis capsular type 2 strains stimulate tumor necrosis factor alpha and interleukin-6 production by murine macrophages. Infect Immun 1999;67:4646-54
18. Wang ZM, Liu C, Dziarski R. Chemokines are the main proinflammatory mediators in human monocytes activated by Staphylococcus aureus, peptidoglycan, and endotoxin. J Biol Chem 2000;275:20260-67
19. Baldwin AC, Kielian T. Persistent immune activation associated with a mouse model of Staphylococcus aureus-induced experimental brain abscess. J Neuroimmunol 2004;151:24-32
20. Moese S, Selbach M, Meyer TF, et al. Cag+ Helicobacter pylori induces homotypic aggregation of macrophage-like cells by up-regulation and recruitment of intracellular adhesion molecule 1 to the cell surface. Infect Immun 2002;70:4687-91
21. Mishra AM, Gupta RK, Jaggi RS, et al. Role of diffusion-weighted imaging and in vivo proton magnetic resonance spectroscopy in the differential diagnosis of ring-enhancing intracranial cystic mass lesions. J Comput Assist Tomogr 2004;28:540-47
22. Mishra AM, Gupta RK, Saksena S, et al. Biological correlates of diffusivity in brain abscess. Magn Reson Med 2005;54:878-85
23. Le Bihan D. Looking into the functional architecture of the brain with diffusion MRI. Nat Rev Neurosci 2003;4:469-80
24. Cartes-Zumelzu FW, Stavrou I, Castillo M, et al. Diffusion-weighted imaging in the assessment of brain abscesses therapy. AJNR Am J Neuroradiol 2004;25:1310-17
25. Bo L, Peterson JW, Mork S, et al. Distribution of immunoglobulin superfamily members ICAM-1, -2, -3, and the beta 2 integrin LFA-1 in multiple sclerosis lesions. J Neuropathol Exp Neurol 1996;55:1060-72
26. Garty BZ, Berliner S, Liberman E, et al. Cerebrospinal fluid leukocyte aggregation in meningitis. Pediatr Infect Dis J 1997;16:647-51
27. Uysal G, Tulek N, Ozhan B. Leukocyte aggregation score ini meningitis and its relationship with cerebrospinal fluid soluble selectin and soluble ICAM-1 levels. J Trop Pediatr 2000;46:381-82
28. Castelli GP, Pognani C, Cita M, et al. Procalcitonin, C-reactive protein, white blood cells and SOFA score in ICU: diagnosis and monitoring of sepsis. Minerva Anestesiol 2006;72:69-80
29. Meisner M, Tschaikowsky K, Palmaers T, et al. Comparison of procalcitonin (PCT) and C-reactive protein (CRP) plasma concentrations at different SOFA scores during the course of sepsis and MODS. Crit Care 1999;3:45-55
30. Ugarte H, Silva E, Mercan D, et al. Procalcitonin used as a marker of infection in the intensive care unit. Crit Care Med 1999;27:498-504
31. Muller B, Becker KL, Schachinger H, et al. Calcitonin precursors are reliable markers of sepsis in a medical intensive care unit. Crit Care Med 2000;28:977-83
32. Luzzani A, Polati E, Dorizzi R, et al. Comparison of procalcitonin and C-reactive protein as markers of sepsis. Crit care Med 2003;31:1737-41
33. Chan YL, Tseng CP, Tsay PK, et al. Procalcitonin as a marker of bacterial infection in the emergency department: an observational study. Crit Care 2004;8:R12-20