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IgE memory B cells identified by the polymerase chain reaction
H Takahama1, S Furusawa, Z Ovary
1New York University Medical School, NY 10016, USA.
Cellular Immunology
|February 25, 1997
Summary
Mice develop memory B cells for immunoglobulin E (IgE) after antigen exposure. These cells, identified by IgE mRNA, can produce IgE antibodies shortly after a booster immunization.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Memory B cells are crucial for long-term immunity, traditionally studied for IgM and IgG responses.
- The existence and characteristics of memory B cells specific for immunoglobulin E (IgE) remain less understood.
Purpose of the Study:
- To investigate the presence and function of memory B cells specific for IgE in a mouse model.
- To determine if IgE memory B cells are generated following immunization and booster doses.
Main Methods:
- Spleen cells were harvested from mice primed and boosted with dinitrophenylated keyhole limpet hemocyanin (DNP-KLH).
- Polymerase chain reaction (PCR) was used to detect IgE mRNA.
- In vitro cultures of spleen cells were performed with and without antigen stimulation.
Main Results:
- IgE mRNA was detectable in spleen cells as early as 1 day after a booster immunization.
- Spleen cells from boosted mice produced anti-DNP IgE antibodies in vitro without additional antigen.
- IgE mRNA and antibody production were not observed in mice primed but not boosted.
Conclusions:
- Mice generate memory B cells specific for IgE, similar to those for IgM and IgG.
- The rapid detection of IgE mRNA and antibody production post-boost indicates swift activation of IgE memory B cells.
- This study expands the understanding of B cell memory to include IgE responses.