B-1 B cells are a self-renewing population of B cells that differ from conv
entional B cells (B-2 cells) in that they are particularly predisposed to a
uto-antibody production(1-3). Although much is known about the signalling p
athways that control B-1-cell growth and development (reviewed in ref. 4),
less is known about why these cells are prone to produce autoreactive antib
odies. Here we show that B-1 cells, like germinal-centre B cells(5-8), can
express recombinase-activating genes 1 and 2 (RAG1 and RAG2) and undergo se
condary V(D)J recombination of immunoglobulin genes. In addition, B cells f
rom autoimmune-prone NZB mice show high levels of RAG messenger RNA and rec
ombination. We propose that secondary immunoglobulin-gene rearrangements ou
tside organized lymphoid organs may contribute to the development of autore
active antibodies.