Eba. Prado et al., REDUCED HUMORAL IMMUNITY IN UREMIC MICE GENETICALLY SELECTED FOR HIGHANTIBODY-RESPONSE, Brazilian journal of medical and biological research, 28(10), 1995, pp. 1081-1087
Biozzi's Selection IV-A mice, genetically selected for 25 generations
for high and low antibody response to sheep red blood cells (SRBC), 2-
3 months old, were made uremic by subtotal nephrectomy and characteriz
ed for antibody production against the selection antigen. T cell activ
ity was evaluated in vitro by lymphocyte proliferation and interleukin
2 (IL 2) production in response to the superantigen staphylococcal en
terotoxin B (SEE). Total and IgM antibody titers (log(2)) were similar
in uremic and non-uremic low responder mice (total antibody: 4.0 +/-
0.6 vs 3.6 +/- 0.6; IgG: 30 +/- 0.7 vs 2.4 +/- 0.4), while uremic high
responders presented a blunted humoral immune response to SRBC when c
ompared with non-uremic animals (total antibody: 10.8 +/- 1.6 ris 13.0
+/- 0.2; IgG: 10.3 +/- 1.5 vs 11.7 +/- 0.3). T cell proliferation and
IL 2 production were similar in uremic and non-uremic groups after SE
E stimulation. The results indicate a genetic effect on sensitivity to
humoral immune response modulation by uremic status, with deficient a
ntibody production despite a normal T cell proliferative response to m
itogen stimulation in short-duration renal failure in high responder m
ice.