B-cell heterogeneity studies have historically focused upon BALB/c mic
e and their derivatives. In contrast, the B cells of DBA/2J mice, a pr
ototype strain for the study of the endogenous minor lymphocyte stimul
atory (Mls) viral superantigen Mls-1(a), have not been extensively inv
estigated. DBA/2J B cells, by functioning as Mls-1(a) antigen-presenti
ng cells, influence their own differentiation and diversity by inducin
g the proliferation and differentiation of specific CD4 T-cell subsets
. In this report, the B cells of DBA/2J and BALB/c mice were compared
for their ability to restore B-cell function in severe combined immuno
deficient (SCID) recipients. Although spleen and bone marrow cells fro
m these strains exhibited similar restoration of serum IgM production,
the transfer of DBA/2J B cells into SCID mice led to greater IgG1 pro
duction. The peritoneal cells of DBA/2J mice consisted of a lower perc
entage of B-1 B cells and were less capable of restoring B-cell functi
on after transfer into SCID recipients. These differences are discusse
d with respect to the possible role of viral superantigens in influenc
ing B-lymphocyte diversity.