Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.2.1.17 (lysozyme)
21,489 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Different immunological parameters (immunoglobulins, complement, lysozyme, and others) were tested in the sera of 65 patients with two forms of chronic glomerulonephritis (mesangiopathic and membranoproliferative GN). The results were compared with values received from 30 healthy human beings. All the data were analyzed carefully by different statistical methods to find out parameters available for a renal immunogram. Out of 14 parameters 4 were indispensable to the GN-groups: alpha 2-macroglobulin, beta-lipoprotein, alpha 1-acid-glycoprotein, lysozyme.
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PMID:[Serum protein determinations in patients with chronic glomerulonephritis and their mathematical-statistical analysis in relation to suitability for renal immunogram]. 244 14

Two new laboratory diagnostic tests for chronic glomerulonephritis and pyelonephritis have been developed. The first one is based on electrophoretic mobility of urinary lysozyme under certain conditions, such as the use of 12% polyacrylamide gel with pH of 4.3 and acid electrode buffer with pH of 4.0. After electrophoresis was discontinued, lysozyme position was determined by lysis of Micrococcus lysodeikticus, used as test agents and added to the gel as a suspension prior to polymerization. Urinary lysozyme was found to be in the anode area of the gel in 95% of patients with chronic pyelonephritis, and in its cathode area in 92% of patients with chronic glomerulonephritis. There was no lysozyme in the urine of normal subjects. The other laboratory technique, the ethanol test, is based on comparative assessment of the degree of urinary opacification after ethanol is added in conditions of neutral reaction (following the addition of physiologic saline) and marked alkaline reaction (following the addition of sodium hydroxide solution). The ratio of optic density of the alkaline specimen to that of the neutral specimen was above 1 in patients with chronic glomerulonephritis, and below 1 in patients with chronic pyelonephritis and normal subjects. Examination of biochemical mechanisms of the proposed tests has demonstrated that the pattern of proteinuria is the most important factor affecting the results.
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PMID:[New methods in the laboratory diagnosis of chronic glomerulonephritis and chronic pyelonephritis]. 271 91

Different electrophoretic mobility of urine lysozyme was established in patients with chronic glomerulonephritis and chronic pyelonephritis during electrophoresis in 12% polyacrylamide gel (gel pH 4.3, electrode buffer pH 4.0). The examination of 128 patients has shown that anode position of lysozyme in electrophoretic tubes is observed in 95% of patients with chronic pyelonephritis, and its anode position in 92% of patients with chronic glomerulonephritis. A method of urine lysozyme electrophoresis under the above conditions was proposed as a noninvasive method of differential diagnosis of chronic glomerulonephritides and chronic pyelonephritides.
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PMID:[Study of electrophoretic mobility of urinary lysozyme in the differential diagnosis of chronic glomerulonephritis and chronic pyelonephritis]. 320 66

In 130 patients with chronic pyelonephritis and 215 patients with chronic glomerulonephritis the serum lysozyme content was established and in 114 and 186, respectively, the enzyme content of their urine tests. Moreover the lysozyme measurement in the serum of 28 patients undergoing haemodialysis was performed. A collective of 50 healthy persons served as comparative group. The lysozyme estimation was performed by means of the agar-diffusion technique after Ossermann and Lawlor in own modification. The average serum lysozyme levels of the patients with pyelonephritis (mean =7.3 micrograms/ml) as well as of the patients with glomerulonephritis (mean = 5.7 micrograms/ml) were significantly increased in contrast to the control group (mean = 4.5 micrograms/ml). Differences could be recognized between the various forms of glomerulonephritis. 34.2% of the patients with pyelonephritis and 37.1% of the patients with glomerulonephritis showed a lysozymuria. In functional restrictions of the kidneys as well as in active forms of the diseases increased concentrations in serum and urine could be established.
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PMID:[Serum and urine lysozyme in chronic pyelonephritis and chronic glomerulonephritis]. 726 23

To determine the diagnostic role of urinary trehalase in chronic glomerular disease, urinary trehalase activity and other urinary markers such as N-acetyl-beta-D-glucosaminidase (NAG), alanine aminopeptidase (AAP), alkaline phosphatase (ALP), gamma-glutamyltranspeptidase (gamma-GTP), lactate dehydrogenase (LDH), lysozyme and beta 2-microglobulin (BMG) were measured in patients with chronic glomerulonephritis, nephrotic syndrome and chronic renal failure. Urinary trehalase activity was significantly increased in chronic glomerular disease, especially nephrotic syndrome, as compared with that in the healthy subjects. The highest incidence of elevated excretion was observed for trehalase with 52% in chronic glomerular disease, followed by NAG. Urinary trehalase activities in the patients were significantly correlated with the urinary levels of protein, NAG and AAP and total score of tubular damage, but not correlated with urinary levels of BMG or lysozyme. In patients with chronic glomerulonephritis and nephrotic syndrome, there was no significant difference in urinary trehalase activities between with and without hematuria. These results indicate that in some patients with chronic glomerular disease, there is tubular involvement as substantiated by elevation of the other urinary enzymes and BMG. Urinary trehalase is elevated more often in these types of disease than other markers of tubular damage.
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PMID:Urinary trehalase activity in chronic glomerulonephritis. 809 31

Proteinuria is one of the bad prognostic indices in renal disease. This study compares the pattern of protein excretion in 10 patients with IgA nephropathy (IgAN), 10 patients with chronic glomerulonephritis approaching end-stage renal failure (ESRF) who still had proteinuria and 10 other patients with diabetic nephropathy (DN) with proteinuria but normal renal function. The pattern of proteinuria was analysed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), isoelectric focusing (IEF) and assayed for orosomucoid, alpha-1-microglobulin, retinol-binding protein, lysozyme, beta-2-microglobulin and N-acetyl-beta-D-glucosaminidase activity. Our data showed much similarity in the pattern of proteinuria between the DN and ESRF groups but significant differences with the IgAN group. The pattern of proteinuria in the IgAN group reflects glomerulonephritis whereas the similar pattern between the ESRF and DN groups may reflect hyperfiltration as well as tubular injury.
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PMID:Pattern of proteinuria in tubular injury and glomerular hyperfiltration. 939 12

The progression of kidney disease to renal failure correlates with infiltration of mononuclear immune cells into the tubulointerstitium. These infiltrates contain macrophages, DCs, and T cells, but the role of each cell type in disease progression is unclear. To investigate the underlying immune mechanisms, we generated transgenic mice that selectively expressed the model antigens ovalbumin and hen egg lysozyme in glomerular podocytes (NOH mice). Coinjection of ovalbumin-specific transgenic CD8+ CTLs and CD4+ Th cells into NOH mice resulted in periglomerular mononuclear infiltrates and inflammation of parietal epithelial cells, similar to lesions frequently observed in human chronic glomerulonephritis. Repetitive T cell injections aggravated infiltration and caused progression to structural and functional kidney damage after 4 weeks. Mechanistic analysis revealed that DCs in renal lymph nodes constitutively cross-presented ovalbumin and activated CTLs. These CTLs released further ovalbumin for CTL activation in the lymph nodes and for simultaneous presentation to Th cells by distinct DC subsets residing in the kidney tubulointerstitium. Crosstalk between tubulointerstitial DCs and Th cells resulted in intrarenal cytokine and chemokine production and in recruitment of more CTLs, monocyte-derived DCs, and macrophages. The importance of DCs was established by the fact that DC depletion rapidly resolved established kidney immunopathology. These findings demonstrate that glomerular antigen-specific CTLs and Th cells can jointly induce renal immunopathology and identify kidney DCs as a mechanistic link between glomerular injury and the progression of kidney disease.
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PMID:Kidney dendritic cell activation is required for progression of renal disease in a mouse model of glomerular injury. 1942 93

Urinary lactic dehydrogenase, alkaline phosphatase and lysozyme determinations were performed on 70 patients with various kidney diseases such as acute and chronic pyelonephritis, acute and chronic glomerulonephritis, idiopathic nephrotic syndrome, diabetic nephropathy, nephrosclerosis, lupus nephritis, analgesic nephropathy, gouty nephropathy, renal tuberculosis, renal lithiasis, and polycystic kidneys. Fifty-three of these patients had elevated levels of urinary lactic dehydrogenase, but this was not of any value in determining the etiology of the renal disease. Similarly, the elevation of alkaline phosphatase in 23 of the 70 had no etiological significance. Neither of these determinations was significant in indicating the degree of renal functional impairment or prognosis. The urinary lysozyme was significantly elevated in only five of the 70 patients and was of no value in indicating the presence or the seriousness of the underlying renal disease.
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PMID:Urinary lactic dehydrogenase, alkaline phosphatase and lysozyme studies in renal disease. 2032 65