The ability of different anti-CD26 monoclonal antibodies to modulate t
he expression of CD26 on human T lymphocytes was investigated. By mean
s of a new non-radioactive method using fluorescein isothiocyanate (FI
TC)-labelled and unlabelled anti-CD26 monoclonal antibodies and flow c
ytometry, we measured the internalization and re-expression of CD26 on
freshly isolated resting human T lymphocytes. The modulation of CD26
surface expression takes place in primarily CD26(+) as well as in CD26
(-) T lymphocytes, indicating the presence of an intracellular CD26 po
ol. In fact, with two different anti-CD26 monoclonal antibodies (Ta1 a
nd M5) intracellular CD26 was detected out of which newly expressed CD
26 might have originated. This intracellular CD26 pool appears to be m
aintained by continuous translation of CD26 mRNA.