EBV and rIL-4 induce T cell-independent IgE production by normal human B cells. We demonstrate here that EBV and IL-4 induced the synthesis of IgE by surface IgE-negative B cell precursors isolated by cell sorting. This result suggests that the induction of IgE by EBV and IL-4 results not merely from the expansion of a precommitted surface IgE-positive B cell population but more likely from IL-4-directed switching to IgE. At the molecular level, IL-4 and EBV induced the appearance of 2.0- and of 1.8-kilobase (kb) RNA bands, both of which hybridized with an o.88-kb HinfI fragment spanning part of the Cε1 exon and the entire Cε2 exon. The 1.8-kb band but not the 2.0-kb band also hybridized with a cloned genomic 0.7-kb SmaI fragment located ~2 kb upstream of Cε. Thus, EBV and IL-4 induced germ-line (1.8-kb) as well as mature (2.0-kb) Cε transcripts. IL-4 by itself induced germ-line Cε transcripts but not mature Cε transcripts in purified normal B cells. IL-4 failed to induce IgE synthesis in established EBV B cell lines and failed to induce 2.0-kb mature Cε transcripts but induced 1.8-kb germ-line Cε transcripts. These data show that IL-4 is sufficient for the induction of Cε germ-line transcription. In contrast, the transcription of mature ε mRNA requires an additional activating signal, provided by infection with EBV. Established EBV transformation results in a dissociation between germ-line Cε transcription and the ability to undergo IgE switching in response to IL-4.
|Original language||English (US)|
|Number of pages||6|
|Journal||Journal of Immunology|
|State||Published - 1990|
ASJC Scopus subject areas
- Immunology and Allergy