Background/Aims: In chronic active liver diseases (CALD) with viral aetiology, a population of plasma cells localised in the piecemeal necrosis areas was previously detected by means of autoradiography after in vitro3H-proline incorporation, a method which proved much more sensitive than conventional immunohistochemical procedures. These plasma cells, characteristically located in niches among hepatocytes, in close contact with collagen fibrils, have been hypothesised to exert a role in fibrogenesis stimulation, and particularly in collagen synthesis, possibly through secretion of lymphokines. Specifically, we investigated the presence of interleukin-1, well known to play a crucial role in inflammation and production of collagen by epithelial cells, and to be present in activated plasma cells of myeloma. Methods: The immunohistochemical localisation of interleukin-l/beta in biopsies of patients suffering from chronic active hepatitis was studied, using an affinity purified rabbit polyclonal antibody. Results: The strongest interleukin-l/i immunostaining was observed in the above-described plasma cell population, identified by anti-immunoglobulin antibodies, and 3H-proline incorporation. Conclusions: The ability of plasma cells to produce interleukin-1 during viral CALD suggests that in these pathologies plasma cells play a major role, mainly of paracrine nature. Interleukiu-1, possibly together with other mediators, might in turn stimulate the production of collagen. Hepatocytes of the piecemeal necrosis area appear to be possible candidates for this synthesis, as they show a significant labelling after 3H-proline incorporation, which is absent from hepatocytes far from necrotic areas.

Hassan, G., Moreno, S., Massimi, M., Di Biagio, P., Stefanini, S. (1997). Interleukin-1-producing plasma cells in close contact with hepatocytes in patients with chronic active hepatitis. JOURNAL OF HEPATOLOGY, 27, 6-17 [10.1016/S0168-8278(97)80273-5].

Interleukin-1-producing plasma cells in close contact with hepatocytes in patients with chronic active hepatitis

MORENO, Sandra;
1997-01-01

Abstract

Background/Aims: In chronic active liver diseases (CALD) with viral aetiology, a population of plasma cells localised in the piecemeal necrosis areas was previously detected by means of autoradiography after in vitro3H-proline incorporation, a method which proved much more sensitive than conventional immunohistochemical procedures. These plasma cells, characteristically located in niches among hepatocytes, in close contact with collagen fibrils, have been hypothesised to exert a role in fibrogenesis stimulation, and particularly in collagen synthesis, possibly through secretion of lymphokines. Specifically, we investigated the presence of interleukin-1, well known to play a crucial role in inflammation and production of collagen by epithelial cells, and to be present in activated plasma cells of myeloma. Methods: The immunohistochemical localisation of interleukin-l/beta in biopsies of patients suffering from chronic active hepatitis was studied, using an affinity purified rabbit polyclonal antibody. Results: The strongest interleukin-l/i immunostaining was observed in the above-described plasma cell population, identified by anti-immunoglobulin antibodies, and 3H-proline incorporation. Conclusions: The ability of plasma cells to produce interleukin-1 during viral CALD suggests that in these pathologies plasma cells play a major role, mainly of paracrine nature. Interleukiu-1, possibly together with other mediators, might in turn stimulate the production of collagen. Hepatocytes of the piecemeal necrosis area appear to be possible candidates for this synthesis, as they show a significant labelling after 3H-proline incorporation, which is absent from hepatocytes far from necrotic areas.
1997
Hassan, G., Moreno, S., Massimi, M., Di Biagio, P., Stefanini, S. (1997). Interleukin-1-producing plasma cells in close contact with hepatocytes in patients with chronic active hepatitis. JOURNAL OF HEPATOLOGY, 27, 6-17 [10.1016/S0168-8278(97)80273-5].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11590/131798
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