To clarify the role of B-12 in the immunological function, serum C3, IgM, I
gG, IgE contents, splenocytes expression of CD4, CD8, and CD4 positive intr
acellular IFN-gamma and IL-4 were examined in B-12-deficient mice, and the
effect of the administration of CH3-B-12 was also studied. Serum C3, IgM an
d IgG contents were lower in B-12-deficient mice than in the control mice.
On the other hand, serum IgE content was sinificantly higher in B-12-defici
ent mice, and the value in CH3-B-12 administered mice, administered CH3-B-1
2 to B-12-deficient mice for 48 h before the end of feeding period, showed
a tendency to recovery. CD4(+)CD8(-) cells and CD4(+)CD8(-)/CD4(-)CD8(+) ra
tio in splenocytes were significantly higher in B-12-deficient mice than in
control mice. CD4(+)IFN-gamma (+) cells was significantly lower in B-12-de
ficient mice than in control mice, and CD4(+)IL-4(+) was significantly high
er in B-12-deficient mice than in control mice. These results suggest that
B-12-deficiency causes CD4(+)CD8(-)T cells shift from the T helper type 1 t
o the T helper type 2, which participate in the IgE production and elevates
CD4(+)CD8(-)/CD4(-)CD8(+) ratio. Thus, B-12 plays a role in maintaining th
e immune function in mice.