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Patents/USRE049514

USRE049514No. USRE049514reissueGranted 5/2/2023

Claims (19)

Claim 1 (Independent)

1. A method comprising: administering a first composition to a subject by an intranasal route, wherein the first composition comprises a vector comprising a polynucleotide encoding a fusion protein, wherein the fusion protein comprises a YscF protein domain, a mature F1 protein domain, and a LcrV protein domain; and administering a second composition to the subject by an intramuscular route, wherein the second composition comprises the fusion protein, wherein the fusion protein is isolated, and wherein the intramuscular administration is after the intranasal administration.

Claim 11 (Independent)

11. A method comprising: administering a composition to a subject by an intranasal route, wherein the composition comprises a vector comprising a polynucleotide encoding a fusion protein, wherein the fusion protein comprises a YscF protein domain, a mature F1 protein domain, and a LcrV protein domain; and administering a second administration of the composition to the subject by an intranasal route.

Claim 12 (Independent)

12. The method of claim 11 wherein the fusion protein comprises at least one linker, wherein the linker is present between two of the domains.

Claim 13 (Independent)

13. The method of claim 11 wherein the fusion protein comprises a His-tag.

Claim 14 (Independent)

14. The method of claim 11 wherein the vector is a replication defective adenovirus vector.

Claim 15 (Independent)

15. The method of claim 14 wherein the defective adenovirus vector is type-5 (Ad5).

Claim 16 (Independent)

16. The method of claim 11 wherein the fusion protein comprises the YscF protein, the mature F1 protein, and the LcrV protein.

Claim 17 (Independent)

17. The method of claim 11 wherein the subject is a human.

Claim 18 (Independent)

18. The method of claim 11 wherein the administering confers immunity to plague caused by Yersinia pestis.

Claim 19 (Independent)

19. The method of claim 18 wherein the plague is pneumonic plague or bubonic plague.

Show 9 dependent claims
Claim 2 (depends on 1)

2. The method of claim 1 wherein the fusion protein comprises at least one linker, wherein the linker is present between two of the domains.

Claim 3 (depends on 1)

3. The method of claim 1 wherein the fusion protein comprises a His-tag.

Claim 4 (depends on 1)

4. The method of claim 1 wherein the vector is a replication defective adenovirus vector.

Claim 5 (depends on 4)

5. The method of claim 4 wherein the defective adenovirus vector is type-5 (Ad5).

Claim 6 (depends on 1)

6. The method of claim 1 wherein the fusion protein comprises the YscF protein, the mature F1 protein, and the LcrV protein.

Claim 7 (depends on 1)

7. The method of claim 1 wherein the intramuscular administration is at least 7 days after the intranasal administration.

Claim 8 (depends on 1)

8. The method of claim 1 wherein the subject is a human.

Claim 9 (depends on 1)

9. The method of claim 1 wherein the administering confers immunity to plague caused by Yersinia pestis.

Claim 10 (depends on 9)

10. The method of claim 9 wherein the plague is pneumonic plague or bubonic plague .

Full Description

No description text available for this patent.

Citations

This patent cites (4)

  • US6261807
  • US9410129
  • US20100209451
  • US2008/045601