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,
,§
*
Department of Pathology,
Geriatrics Center, and
Institute of Gerontology, University of Michigan, Ann Arbor, MI 48109; and
§
Ann Arbor DVA Medical Center, Ann Arbor, MI 48109
We describe a system for the in vitro production of Ag-specific
mouse CD4 cell lines from unprimed mice. Purified
CD4+CD45RBhigh T cells were exposed to
Ag-pulsed accessory cells in serum-free medium for 24 h; cultured
in the absence of Ag and in the presence of serum, IL-2, dexamethasone,
and Abs to IL-10 for an additional 4 days; and then re-exposed to the
original sensitizing Ag. The presence of dexamethasone and Abs to IL-10
during the initial expansion stage appeared to be critical for the
ability of the stimulated and expanded T cells to respond to
restimulation with the same Ag. Repeated cycles of in vitro stimulation
led to increased specificity for the sensitizing Ag (in the current
case, pigeon cytochrome c), a decline in production
of IL-2 and IFN-
, and increased production of IL-4, IL-5, and IL-10.
This culture protocol provides a test system for exploration of factors
that regulate the conversion of naïve cells to memory cells and
the development of specific immune responses to protein Ags. The data
are consistent with models that implicate glucocorticoids as regulators
of immune response specificity.
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