T cell tolerance can be induced by B cell presentation of Ags to naive
T cells. To further characterize this mechanism of T cell tolerance i
nduction, we have investigated the effects of injecting mice with an i
ntact rat IgC2a Ab, which binds to the B cell low-affinity Fc epsilon
receptor (CD23), on the responsiveness of B cells and T cells to rat I
gG2a. Our observations indicate that 1) intravenous, subcutaneous, or
intraperitoneal injection of this Ab induces antigen-specific B cell a
nd T cell tolerance; 2) both forms of tolerance are induced more compl
etely by injection of rat IgC2a anti-CD23 mAb than by injection of an
equal dose of a control rat IgG2a Ig; and 3) reduced responsiveness to
Ag is seen as early as 1 to 3 days after anti-CD23 mAb injection and
reaches maximum levels by 7 days after injection. Although tolerance i
nduced by the injection of soluble proteins has been reported to be ch
aracterized by reduced production of IL-2 and IFN-gamma, but normal pr
oduction of IL-4, injection of mice with rat IgG2a anti-mouse CD23 mAb
greatly decreases the IL-4 response to a rat IgG2a immunogen that nor
mally induces a large IL-4 response.