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Hepatocellular apoptosis associated with cytotoxic T/natural killer‐cell infiltration in chronic active EBV infection
Author(s) -
Nomura Yuko,
Kimura Hiroshi,
Karube Kennosuke,
Yoshida Shiro,
Sugita Yasuo,
Niino Daisuke,
Shimizu Kei,
Kimura Yoshizo,
Aoki Ryosuke,
Kiyasu Junichi,
Takeuchi Masanori,
Hashikawa Keiko,
Hirose Shinichi,
Ohshima Koichi
Publication year - 2009
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1111/j.1440-1827.2009.02391.x
Subject(s) - cytotoxic t cell , granzyme b , granzyme , biology , perforin , pathology , spleen , apoptosis , cd3 , natural killer cell , cd8 , lymph node , immunology , antigen , medicine , biochemistry , in vitro
The aim of the present study was to identify the mechanism of hepatocellular apoptosis induced by EBV‐infected cytotoxic T/natural killer (NK) cells in chronic active EBV infection (CAEBV). Eight patients with CAEBV were studied, and infected T‐cell expansion and NK‐cell expansion were detected in four patients each. Biopsy or necropsy was performed on lymph node, liver, or spleen, and each specimen was subjected to immunohistochemical double staining of CD3 plus caspase‐3 with the addition of cytotoxic markers of T‐cell restricted intracellular antigen‐1 (TIA‐1), perforin, and granzyme B, as well as EBV in situ hybridization (EBV‐ISH). In the liver, some of the infiltrating CD3‐positive lymphocytes stained positively for EBV‐ISH and cytotoxic markers. Double staining of CD3 plus caspase‐3 indicated caspase‐3 positive hepatocytes with apoptotic features, accompanied by extensive infiltration of CD3‐positive cells, which were directly attached to the apoptotic caspase‐3 positive hepatocytes. In contrast, far fewer cells stained positive for caspase‐3 in lymph node and spleen than in liver. The present findings suggest that in patients with CAEBV, cytotoxic T/NK cells may directly induce hepatocytes to undergo apoptosis more frequently than they do cells in other organs of the reticulo‐endothelial system.