Background & Aims: Activation-induced cell death is involved in regula
ting peripheral T-cell function. Understanding the kinetics of these T
cells is important to elucidate the pathogenesis of chronic hepatitis
B, which is mediated by cellular immune mechanisms. Methods: Subtle a
poptotic cells in CD3(+) cells were discriminated by flow-cytometric a
ssay using freshly obtained and in vitro recombinant hepatitis B core
antigen-stimulated peripheral lymphocytes from patients with chronic h
epatitis B. Results: The ratio of apoptotic cells in freshly obtained
CD3(+) cells was significantly higher during the decreasing phase than
increasing phase of serum alanine aminotransferase activity in each p
atient, and apoptosis of CD3(+) cells was induced by stimulation with
recombinant hepatitis B core antigen. Conclusions: Activation-induced
cell death in peripheral T cells was found in chronic hepatitis B viru
s infection, similar to some other viral infections. The apoptosis in
T cells during the decreasing phase of serum alanine aminotransferase
activity results in a vast amount of T-cell deletion that may weaken T
-cell function of cytotoxicity over hepatitis B virus-infected hepatoc
ytes. Thus, activation-induced cell death is considered an important m
odulator in down-regulating the ''burst'' of responding T cells in pat
ients with chronic hepatitis B.