The growth kinetics and population dynamics of recombinant interleukin
-2 (rlL-2) stimulated human natural killer (NK) cell-enriched populati
ons were studied in vitro. The NK-enriched population was obtained fro
m normal peripheral blood mononuclear cells (PBMNC) by immunomagnetic
bead depletion of CD3(+) and CD5(+) T cells. The growth kinetics of NK
cells, T cells, monocytes, and total cells are shown. In the absence
of PBMNC accessory cells, the NK-enriched population showed limited ex
pansion. In the presence of PBMNC accessory cells, the NK-enriched pop
ulation expanded threefold more than in the absence of accessory cells
due to increased NK cell growth rate and increased duration of expone
ntial growth. Using a Transwell system, which cell populations by a po
lycarbonate accessory cells were shown to act on the NK-enriched popul
ation via a diffusible factor. Accessory cell conditioned media was ab
le to replace the accessory cell population to stimulate NK cell expan
sion. A monocyte-enriched population prepared by sheep red blood cell
resetting of T cells was extensively phenotyped and compared with the
NK-enriched populations. Although the final cultured cells were phenot
ypically homogeneous for CD56(+)/CD3(-) NK cells, the initial NK precu
rsor populations appear to be different. Namely, the NK cell precursor
s in the monocyte-enriched population were predominantly CD56(+)/CD2(-
). Kinetic equations were formulated for this culture system and the e
ffects of major culture variables are investigated. (C) 1994 John Wile
y and Sons, Inc.