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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 390 (1981), S. 259-272 
    ISSN: 1432-2307
    Keywords: Renal amyloidosis ; Early lesions ; Amyloid by electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Our investigations on early glomerular changes in renal amyloidosis showed the following: 1. In some renal biopsies, amyloid was demonstrated in the mesangial matrix predominantly and could be seen penetrating through the basememt membrane of the mesangial region into the subepithelial space of adjacent glomerular capillaries. 2. In other biopsies, showing the same severity of amyloidosis, deposits were demonstrated in the mesangium and in the capillary walls distant from the mesangium on both sides of the basememt membrane. There was no apparent connection between the deposits in these two areas. 3. On the basis of the morphological changes found in the cytoplasm of the mesangial cells, the glomerular epithelial cells and partly also in the endothelial cells, supported by our electron microscopic findings in the immediate vicinity of these cells, we come to the conclusion that amyloid in the glomerulus is formed from amyloid precursors brought via the blood stream. 4. Amyloid fibrils may be formed in the extracellular space of the glomerulus under the influence of lysosomal enzymes released from epithelial, mesangial and perhaps endothelial cells, by action of these enzymes on extracellularly deposited amyloid precursors.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1831
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The efficacy of a herpes simplex virus type 1 (HSV-1) envelope antigen (EAG) preparation against HSV infection was studied in T cell competent and T cell deficient mice. Immuno-competent mice were successfully protected against herpes simplex virus type 1 (HSV-1) or type 2 (HSV-2) infection when immunized 2 weeks prior to this infection with a heat-inactivated whole virus preparation or a HSV-1 envelope antigen (HSV-1 EAG) preparation. Since HSV-1 EAG was considerably less effective than the whole virus preparation, a polyriboinosinic-polyribocytidylic acid complex with poly-L-lysine and carboxymethylcellulose (PICLC) was used as adjuvant. Immunization with HSV-1 EAG plus PICLC resulted in a pronounced increase of this protection rate as compared with that obtained after immunization solely with HSV-1 EAG. PICLC alone, however, offered no protection when given 2 weeks before challenge. In T cell deficient nu/nu mice no protection was achieved with HSV-1 EAG while their T cell competent, heterozygous littermates were protected. From these results it may be concluded that T cell competence is a prerequisite for establishing a protective immunity against HSV infection after immunization with HSV-1 EAG.
    Type of Medium: Electronic Resource
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