Viral vectored immunocontraception: screening of multiple fertility antigens using murine cytomegalovirus as a vaccine vector.

Vaccine

Microbiology and Immunology, School of Biomedical, Biomolecular and Chemical Sciences, M502, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia.

Published: January 2007

AI Article Synopsis

  • Mouse cytomegalovirus (MCMV) has been shown to effectively induce long-term infertility in female mice when expressing the murine zona pellucida 3 (mZP3) antigen, though comparisons among different antigens have been limited.
  • Various antigens, including bone morphogenic protein 15 (BMP15) and oviduct glycoprotein (OGP), were tested for their ability to sterilize female mice, but only mZP3, particularly in its full-length or ubiquitin-tagged form, was effective.
  • The study highlights that while MCMV is a promising vector for viral vectored immunocontraception (VVIC), further empirical testing of antigens is necessary, with one poly

Article Abstract

Mouse cytomegalovirus (MCMV) has previously been used as a vaccine vector for viral vectored immunocontraception (VVIC). MCMV expressing murine zona pellucida 3 (mZP3) induces long term infertility in up to 100% of female BALB/c mice following a single inoculation. Whilst a large number of antigens have been investigated as potential immunocontraceptive vaccines, it has been difficult to compare these antigens as few studies have used identical approaches or even animal species. Here a range of protein and polyepitope antigens, all expressed by MCMV, were tested for the ability to sterilise female mice. The antigens tested were bone morphogenic protein 15 (BMP15), oviduct glycoprotein (OGP) and ubiquitin-tagged mZP3. In addition, four polyepitope constructs that contain rodent or mouse specific epitopes were tested. This study found that when expressed by an MCMV vector, only full-length mZP3 or ubiquitin-tagged mZP3 induced infertility in female mice. BMP15 and OGP had no effect. Of the four polyepitopes tested, one had a partial effect on fertility. These data indicate that while MCMV is an effective vector for VVIC, the antigen used needs to be tested empirically. The partial infertility seen in mice infected with one of the polyepitope vaccines is a promising finding suggesting that it may be possible to combine a species specific virus with a species specific antigen for use as a disseminating mouse control agent.

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Source
http://dx.doi.org/10.1016/j.vaccine.2006.08.021DOI Listing

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