CD8+ T cells infiltrating into bile ducts in biliary atresia do not appear to function as cytotoxic T cells: a clinicopathological analysis

A Faiz Kabir Uddin Ahmed, H Ohtani… - The Journal of …, 2001 - Wiley Online Library
A Faiz Kabir Uddin Ahmed, H Ohtani, M Nio, N Funaki, S Shimaoka, H Nagura, R Ohi
The Journal of Pathology, 2001Wiley Online Library
It is speculated that immune mechanisms are involved in bile duct damage in biliary atresia
(BA), as in primary biliary cirrhosis (PBC). In BA, however, no reports have described the in
situ distribution of cytotoxic T lymphocytes (CTLs) using specific markers, nor has the clinical
association been clarified. The present study describes the immunohistochemical
distribution of CD8+ T cells and the relevant markers [perforin, granzyme B, FasL (CD95L)]
in 47 cases of BA operated upon at days 12–79. The results were compared with those of …
Abstract
It is speculated that immune mechanisms are involved in bile duct damage in biliary atresia (BA), as in primary biliary cirrhosis (PBC). In BA, however, no reports have described the in situ distribution of cytotoxic T lymphocytes (CTLs) using specific markers, nor has the clinical association been clarified. The present study describes the immunohistochemical distribution of CD8+ T cells and the relevant markers [perforin, granzyme B, FasL (CD95L)] in 47 cases of BA operated upon at days 12–79. The results were compared with those of PBC. In BA, CD8+ T cells infiltrated bile ducts in a way similar to that observed in PBC. However, in sharp contrast to PBC, none of the inflammatory cells infiltrating into the bile ducts in BA expressed cytotoxic markers such as perforin, granzyme B, or Fas ligand (FasL). Clinical follow‐up of patients with BA revealed that a greater degree of infiltration of bile ducts by CD8+ T cells is associated with better liver function. Taken together, these data suggest the absence of direct CTL activity against bile ducts in BA in the postnatal period. Copyright © 2000 John Wiley & Sons, Ltd.
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