Fertilization antigen (FA-1) is a testis/sperm-specific glycoprotein that is present on sperm of various mammalian species including man and mouse and has a role in fertilization. It is involved in human immunoinfertility and the recent clinical trial indicates that it may have clinical applications in specific diagnosis and treatment of immunoinfertile men. The cDNAs encoding for murine and human FA-1 antigens have been cloned and sequenced. Active immunization of female mice with murine recombinant(r) FA-1 antigen or with another recently identified novel sperm-specific dodecamer synthetic peptide, designated as YLP12, causes an overall 70% reduction, rather than a complete block, of fertility with either vaccine, due to inter-individual variability of the immune response. The present proposal has four specific aims and will focus on obtaining FA-l-reactive human monoclonal antibodies that could be used as a passive immunocontraceptive to avoid variability of the immune response, and on testing the bivalent vaccine having FA-1 antigen and YLP12 together in a single formulation to obtain a complete block in actively immunized female mice.
Specific aim 1 is to construct a combinatorial phage display library having y1 heavy (H) and kappa light (L) chains cDNA inserts of Fab antibodies, reverse-transcribed from RNA isolated from peripheral lymphocytes of immunoinfertile men.
Specific aim 2 is to select the human rFA-1 antigen-reactive clones from the library using the panning procedure and sequence the Hand L-chain inserts of the selected clones.
Specific aim 3 is to investigate the immunobiological effects of the Fab antibodies secreted by the human rFA-1 antigen-reactive clones by using various assays.
Specific aim 4 is to investigate the immunocontraceptive effect of the bivalent vaccine, having murine rFA-1 antigen and synthetic YLP12 peptide in a single formulation, in actively immunized female mice. Besides enabling us to study the structure-function relationship, these studies will examine the utility of recombinant FA-1 antigen and synthetic YLP12 peptide, and recombinant human antibodies in immunocontraception and immunoinfertility in humans. ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD024425-18
Application #
7226967
Study Section
Reproductive Endocrinology Study Section (REN)
Project Start
1988-12-01
Project End
2010-03-31
Budget Start
2007-04-01
Budget End
2010-03-31
Support Year
18
Fiscal Year
2007
Total Cost
$249,183
Indirect Cost
Name
West Virginia University
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
191510239
City
Morgantown
State
WV
Country
United States
Zip Code
26506
Lemons, Angela R; Naz, Rajesh K (2012) Birth control vaccine targeting leukemia inhibitory factor. Mol Reprod Dev 79:97-106
Lemons, Angela R; Naz, Rajesh K (2011) Contraceptive vaccines targeting factors involved in establishment of pregnancy. Am J Reprod Immunol 66:13-25
Naz, Rajesh K (2011) Antisperm contraceptive vaccines: where we are and where we are going? Am J Reprod Immunol 66:5-12
Williams, Ryan M; Naz, Rajesh K (2010) Novel biomarkers and therapeutic targets for prostate cancer. Front Biosci (Schol Ed) 2:677-84
Rodgers-Melnick, Eli B; Naz, Rajesh K (2010) Male-biased genes of Drosophila melanogaster that are conserved in mammalian testis. Front Biosci (Elite Ed) 2:841-8
Naz, Rajesh K; Catalano, Briana (2010) Gene knockouts that affect female fertility: novel targets for contraception. Front Biosci (Schol Ed) 2:1092-112
Naz, Rajesh K; Dhandapani, Latha (2010) Identification of human sperm proteins that interact with human zona pellucida3 (ZP3) using yeast two-hybrid system. J Reprod Immunol 84:24-31
Naz, Rajesh K; Rowan, Shon (2009) Update on male contraception. Curr Opin Obstet Gynecol 21:265-9
Naz, Rajesh K (2009) Status of contraceptive vaccines. Am J Reprod Immunol 61:11-8
Naz, Rajesh K; Engle, Alexis; None, Rajnee (2009) Gene knockouts that affect male fertility: novel targets for contraception. Front Biosci (Landmark Ed) 14:3994-4007

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