The role of the cellular immune response to human T-cell lymphotropic virus
type I (HTLV-I) is not fully understood. The low level of HTLV-I protein e
xpression in peripheral blood lymphocytes has led to the widely held belief
that HTLV-I is transcriptionally silent in vivo. However, most HTLV-I-infe
cted individuals mount a strong and persistently activated cytotoxic T-lymp
hocyte (CTL) response to the virus; this observation implies that there is
abundant chronic transcription of HTLV-I genes. Here we Show that HTLV-I Ta
x protein expression rises quickly in freshly isolated peripheral blood lym
phocytes, but that expressing cells are rapidly killed by CTLs. Mathematica
l analysis of these results indicates that the CTL response is extremely ef
ficient and that the half-life of a Tax-expressing cell is less than a day
We propose that HTLV-I protein expression in circulating lymphocytes is und
etectable by current techniques because of the efficiency of the CTL-mediat
ed immune surveillance in vivo.