A. Ben-smith et al., The relationship between circulating and intestinal Heligmosomoides polygyrus-specific IgG(1) and IgA and resistance to primary infection, PARASITE IM, 21(8), 1999, pp. 383-395
Specific serum and intestinal immunoglobulin (Ig)G(1) and IgA responses to
Heligmosomoides polygyrus wc re measured in a panel of seven inbred mouse s
trains which exhibit 'rapid' (<6 weeks (SWRxSJL)F-1), 'fast' (< 8 weeks, SJ
L and SWR), 'intermediate' (10-20 weeks, NIH and BALB/c) or 'slow' (>25 wee
ks, C57BL/10 and CBA) resolution of primary infections. Mice with 'rapid',
fast' or 'intermediate' response phenotypes produced greater serum and inte
stinal antibody responses than those with 'slow' phenotypes. The F-1 hybrid
s ((SWR x SJL)F-1) of two fast' responder strains showed the earliest antib
ody response with maximum titres evident within 6 weeks of infection. There
was a negative correlation between the serum IgG(1) responses and worm bur
dens in individual mice within a number of mouse strains, and also between
serum IgG(1) and IgA responses and worm burdens in the 'rapid' ((SWR x SJL)
F-1) responder strain. The presence off IgG(1) in the gut was found to be d
ue to local secretion rather than plasma leakage. Using Western immunoblott
ing, serum IgG(1) from 'rapid' and 'fast' responder but not 'slow' responde
r mice was found to react with low molecular weight antigens (16-18 kDa) in
adult worm excretory/secretory products.