Cj. Flickinger et al., TEMPORAL RECOGNITION OF SPERM AUTOANTIGENS BY IGM AND IGG AUTOANTIBODIES AFTER VASECTOMY AND VASOVASOSTOMY, Journal of reproductive immunology, 27(2), 1994, pp. 135-150
Temporal patterns of IgM and IgG autoantibodies to sperm proteins were
studied by western blot analysis at intervals after bilateral vasecto
my, vasectomy followed one month later by vasovasostomy, or sham opera
tions. Responses were detected to eight major autoantigens at 21-23, 3
6, 41, 51, 57, 63, 68-71 and 75-83 kDa, by study of staining patterns
of sequential serum samples from individual animals and by analysis of
the incidence of reaction to each protein. The four lower molecular w
eight antigens (21-23, 36, 41 and 51 kDa) provoked mainly Ige response
s. The strongly stained set of higher molecular weight antigens (57, 6
3, 68-71 and 75-83 kDa) tended to show more clearly defined temporal p
atterns of IgM followed by IgG response, including a high incidence of
IgM antibody at the 2-week interval. Three of the larger peptides (57
, 63 and 68-71 kDa) appeared highly immunogenic, since some reactions
were detected even in sham-operated rats. The classical patterns of Ig
M and IgG antibody responses to the majority of the dominant sperm aut
oantigens are in accord with the hypothesis that vasectomy mimics immu
nization with spermatozoa. The high incidence of IgM antibodies in the
earliest sample, taken 2 weeks after vasectomy, suggests that the ini
tial immunizing event takes place within about a week after the operat
ion. Vasovasostomy did not bring about a decrease in antisperm antibod
ies. Instead, some animals demonstrated an increased reaction to certa
in antigens after reversal of vasectomy, even though the vasovasostomi
es were anatomically successful.