INHIBITION OF FERTILITY IN FEMALE MICE BY IMMUNIZATION WITH A B-CELL EPITOPE, THE SYNTHETIC SPERM PEPTIDE, P10G

Citation
Mg. Orand et al., INHIBITION OF FERTILITY IN FEMALE MICE BY IMMUNIZATION WITH A B-CELL EPITOPE, THE SYNTHETIC SPERM PEPTIDE, P10G, Journal of reproductive immunology, 25(2), 1993, pp. 89-102
Citations number
20
Categorie Soggetti
Reproductive Biology",Immunology
ISSN journal
01650378
Volume
25
Issue
2
Year of publication
1993
Pages
89 - 102
Database
ISI
SICI code
0165-0378(1993)25:2<89:IOFIFM>2.0.ZU;2-V
Abstract
Human patient sera containing antisperm antibodies (from vasectomized men and infertile women) immunologically react with the synthetic pept ide P10G (PGGGTLPPSG), and affinity purified antibodies to P10G (anti- P10G) react with human spermatozoa (O'Rand et al., 1990). In this stud y P10G was used to elicit antibodies and the effect of the antibodies on fertility in female mice determined. The P10G sequence is derived f rom the 14-kDa rabbit sperm autoantigen, RSA (O'Rand and Widgren, 1990 ). The results of this study demonstrate that female mice can become i nfertile when immunized with the synthetic peptide P10G conjugated to the carrier protein keyhole limpet hemocyanin (KLH). However, the resu lts also show that it is important to distinguish those mice with high serum antibody levels from those with lower levels. Infertility was c learly apparent in the high titer subgroup with an 80% decrease in pre gnancy rate during the last of three matings and a 71% decrease in lit ter size over all three matings when compared to the low titer subgrou p or the control groups. Significantly, mice immunized with P10G witho ut carrier protein show no detectable antigen specific proliferation o f lymph node cells in response to 100 mu M of the peptide. P10G is not a T-cell epitope, but rather a B-cell epitope and it does not elicit an autoimmune response in the female mouse. This demonstration in mice is an important first step in the development of a safe human immunoc ontraceptive vaccine.