Treatment and prevention of
View Patent ↗The present invention is drawn to the nucleic and amino acid sequences encoding vaginolysin (VLY) toxin from Gardnerella vaginalis , and biologically active fragments and variants thereof. The invention is also directed to anti-VLY antibodies and to their use therapeutically and in a new ELISA assay of VLY toxin. Other embodiments of the invention are directed to VLY toxoids and to vaccines that use the new VLY toxoids as immunogens.
1. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by a single amino acid substitution consisting of a tryptophan residue at position 480, or an immunologically active fragment thereof comprising the single amino acid substitution.
2. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by a single amino acid substitution consisting of an isoleucine residue at position 500, or an immunologically active fragment thereof comprising the single amino acid substitution.
3. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by a single amino acid substitution consisting of an arginine [R] at position 471, or an immunologically active fragment thereof comprising the single amino acid substitution.
4. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by a single amino acid substitution consisting of a cysteine [C] at position 473, or an immunologically active fragment thereof comprising the single amino acid substitution.
5. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by two amino acid substitutions consisting of an arginine [R] at position 471 and a cysteine [C] at position 473 or an immunologically active fragment thereof comprising the two amino acid substitutions.
6. An isolated and purified pore-forming toxoid of vaginolysin from G. vaginalis , which toxoid differs from vaginolysin identified by SEQ ID NO: 2 by a two amino acid substitutions consisting of a tryptophan [W] at position 480, and an isoleucine at position 500, or an immunologically active fragment thereof comprising the two amino acid substitutions.
7. The isolated and purified pore-forming toxoid of claim 6 , further comprising a third amino acid substitution of a cysteine [C] at position 473 of SEQ ID NO. 2 or an immunologically active fragment thereof comprising the three amino acid substitutions.
8. A method of eliciting an immune response in an animal to G. vaginalis vaginolysin, comprising introducing into the animal a composition comprising the isolated and purified G. vaginalis vaginolysin toxoid protein or an immunologically active fragment thereof as claimed in one of claims 1 - 7 .
9. A composition for treating G. vaginalis and bacterial vaginosis infections, comprising the isolated and purified G. vaginalis vaginolysin pore-forming toxoid protein or an immunologically active fragment thereof as claimed in one of claims 1 - 7 .
10. A method of treating a G. vaginalis infection or bacterial vaginosis in a patient, by administering to the patient a therapeutically effective amount of the G. vaginalis vaginolysin pore-forming toxoid protein or an immunologically active fragment thereof as claimed in one of claims 1 - 7 .
11. A pharmaceutical formulation comprising the isolated and purified G. vaginalis vaginolysin pore-forming toxoid protein or an immunologically active fragment thereof as claimed in one of claims 1 - 7 .
12. The pharmaceutical formulation of claim 11 , formulated for systemic administration.
13. The pharmaceutical formulation of claim 11 , formulated for topical administration.