Tissue Localization of Toll‐Like Receptors in Biopsy Specimens of Liver from Children Infected with Hepatitis C Virus

Toll‐like receptors (TLR) are important tools of innate immunity, localized mainly on cells of the immune system, but also have been shown on cells of other origin. In the current study, they have been searched in biopsy specimens of liver from children bearing chronic viral hepatitis of C type (HCV...

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Veröffentlicht in:Scandinavian journal of immunology 2005-10, Vol.62 (4), p.407-412
Hauptverfasser: Mozer‐Lisewska, I., Sluzewski, W., Kaczmarek, M., Jenek, R., Szczepanski, M., Figlerowicz, M., Kowala‐Piaskowska, A., Zeromski, J.
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Sprache:eng
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Zusammenfassung:Toll‐like receptors (TLR) are important tools of innate immunity, localized mainly on cells of the immune system, but also have been shown on cells of other origin. In the current study, they have been searched in biopsy specimens of liver from children bearing chronic viral hepatitis of C type (HCV). TLR2, TLR3 and TLR4 were traced by means of polyclonal antibodies and avidin‐biotin complex (ABC) immunohistochemistry. Besides, mRNA for TLR was looked for using specific primers and polymerase chain reaction. Several controls, including neutralization of primary antibody with respective blocking peptide, confirmed the specificity of the immunohistochemical reaction. All TLR tested could be visualized in a focal distribution in single hepatocytes and some cells of inflammatory infiltrates. There was no reaction whatsoever in liver samples not infected with hepatotropic virus. In molecular studies, mRNA for TLR2 and TLR4 was detected in both noninfected and hepatitis B virus‐infected established cell lines of human hepatoma as well as in HCV+ biopsy samples. These data indicate that TLR can be traced in liver cells, both at the protein and at the mRNA level. Their irregular and focal distribution in HCV+, but not in HCV–, liver suggests some role of TLR in the pathogenesis of chronic viral hepatitis, at least in children.
ISSN:0300-9475
1365-3083
DOI:10.1111/j.1365-3083.2005.01670.x