Recent data provide evidence that antigen-specific CD4(+) T-cell clone
s or antigen-activated T-cell lines can kill antigen-presenting cells
(APC). We focused our studies on monocytes acting as APC in cultures o
f T cells freshly isolated from peripheral blood. The presence of mono
cytes in culture was monitored by their ability to emit light during p
hagocytosis of latex particles (latex-induced chemiluminescence). Usin
g this approach as well as flow cytometry, evidence is presented that
monocytes are eliminated from cultures with T cells activated with rec
all antigens (PPD or TT). The mechanism of monocyte elimination involv
ed apoptosis as judged from in situ detection of DNA strand breaks by
the terminal deoxynucleotidyl transferase assay. The antigen- but not
lectin-dependent monocyte elimination was MHC-restricted and mediated
by CD4(+) T lymphocytes. This finding supports the hypothesis that eli
mination of APC is a general phenomenon during T-cell activation and m
ay represent an important immunoregulatory mechanism.