M. Karaca et al., Genetic line and major histocompatibility complex effects on primary and secondary antibody responses to T-dependent and T-independent antigens, POULTRY SCI, 78(11), 1999, pp. 1518-1525
The effects of MHC and nonMHC (background) genetics on the kinetics of prim
ary and secondary antibody responses to T-cell-dependent (SRBC) and T-cell-
independent [Brucella abortus (BA)] antigens were investigated. Eight genet
ic groups were represented, with four homozygous MHC haplotypes [B-1-lrGAT(
low) (IrGAT = immune response to GAT locus); B-1-IrGAT(high); B-19-IrGAT(lo
w); B-19-IrGAT(high)] on two genetic backgrounds, the SI and G lines, Birds
were injected simultaneously with BA and SRBC at 4 and 7 wk of age, and bl
ood samples were taken weekly from 4 to 10 wk of age for measurement of tot
al agglutinating serum antibody levels. A quadratic equation and its first
derivative were computed for each bird to approximate individual curve para
meters: y max, the maximum titer; t max, the time required to achieve y max
; and c coefficient, the rate of decline in the titer. Curve parameters of
birds from different lines were analyzed separately by using the General Li
near Model procedure. A second analysis that included line effect evaluated
the nonMHC gene effects and their interactions with erythrocyte antigen B
locus (Ea;B) or IrGAT. In the S1 line, there was an interaction (P < 0.05)
between MHC haplotypes and sex for primary response to BA. In contrast, the
re were no significant main effects nor interactions in the G Line backgrou
nd for primary and secondary responses to BA and SRBC. There was an effect
(P < 0.05) of line background on y max for primary BA and for secondary SRB
C responses. A positive correlation (P < 0.05) was found between the c coef
ficients of BA and SRBC secondary responses, suggesting that the Tate of de
cline in the secondary response is similar between these T-dependent and T-
independent responses. The overall results of this study indicate complex i
nteractions between specific MHC alleles and the nonMHC background of the L
ines in which they are studied.