Antigen (Ag) is retained for long periods of time in secondary lymphoi
d tissues in the form of immune complexes on follicular dendritic cell
s (FDC). Ag retained on FDC is thought to play a role in maintaining a
ntibody (Ab) responses in vivo. A model for study of Ab production ind
uced by retained Ag in vitro, is the spontaneous Ab response. In this
response, specific Ab production is induced spontaneously (no exogenou
s Ag needed) in cultures derived from secondary lymphoid tissues conta
ining persisting Ag. Specific IgG is spontaneously induced and we reas
oned that FDC may also play a role in the maintenance of specific IgE
responses. To test this hypothesis, we monitored spontaneous anti-oval
bmin (OVA) IgE production in cultures of lymph node (LN) fragments fro
m OVA-immunized mice. In addition, highly enriched preparations of OVA
bearing FDC were added to OVA-specific memory cells in an attempt to
stimulate OVA-specific IgE production. Months after secondary immuniza
tion, anti-OVA IgE responses were spontaneously induced when fragments
from draining LN were placed into culture. Furthermore, FDC bearing O
VA from draining LN induced anti-OVA ISE production when incubated wit
h spleen cells from OVA-immune mice whereas identical cultures with FD
C bearing environmental Ag from non-draining LN of the OVA immune anim
als did not. The anti-OVA IgE responses were elicited only in cultures
containing OVA-immune memory cells indicating that specific memory ce
lls were critical for these anti-OVA IgE responses. Removal of FDC fro
m cultures with an FDC-specific mAb dramatically decreased anti-OVA Ig
E production. These studies demonstrate that FDC can induce specific m
emory T and B cells to produce IgE and help support the concept that F
DC-associated antigen may be involved in the long-term maintenance of
specific IgE responses.