CBA/H mice produced serum anti-pig IgG(1), IgG(2a), and IgG(2b) follow
ing xenotransplantation of pig proislets beneath the kidney capsule; a
nti-pig IgM was present as pre-existing antibody in the serum of norma
l CBA/H mice and was also produced in response to pig proislet xenogra
fts, Serum anti-pig IgG(3) was not detected post-xenotransplantation.
Rejection of pig proislet xenografts and the production of anti-pig Ig
G(1), IgG(2a), and IgG(2b) isotypes were CD4 T cell-dependent, The cap
acity for adoptively transferred hyperimmune CBA/H mouse anti-pig PBL
serum to induce the rejection of intact pig proislet xenografts in CD4
T cell-depleted mice was dose dependent and correlated with markedly
elevated levels of serum anti-pig IgG(3), Levels of anti-pig IgG(1), I
gG(2a), IgG(2b), and IgM comparable to control mice acutely rejecting
pig proislet xenografts and achieved following adoptive transfer of hy
perimmune serum did not correlate with induced xenograft rejection, Th
ese findings suggest that anti-pig Ig isotypes produced during the con
ventional process of acute proislet xenograft rejection do not play a
major role in mediating graft damage. The acute rejection of pig prois
let xenografts in the absence of serum anti-pig Ig in mu MT-/-hosts co
nfirmed that anti-pig antibody is not essential for proislet xenograft
destruction.