FOLLICULAR DENDRITIC CELLS AND THE MAINTENANCE OF IGE RESPONSES

Citation
Slt. Helm et al., FOLLICULAR DENDRITIC CELLS AND THE MAINTENANCE OF IGE RESPONSES, European Journal of Immunology, 25(8), 1995, pp. 2362-2369
Citations number
39
Categorie Soggetti
Immunology
ISSN journal
00142980
Volume
25
Issue
8
Year of publication
1995
Pages
2362 - 2369
Database
ISI
SICI code
0014-2980(1995)25:8<2362:FDCATM>2.0.ZU;2-A
Abstract
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.