Attenuated mannheimia haemolytica vaccines and methods of making and use

US9675682B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9675682-B2
Application numberUS-201614991003-A
CountryUS
Kind codeB2
Filing dateJan 8, 2016
Priority dateNov 8, 2012
Publication dateJun 13, 2017
Grant dateJun 13, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides attenuated M. haemolitica strains that elicit an immune response in animal against M. haemolitica , compositions comprising said strains, methods of vaccination against M. haemolitica , and kits for use with such methods and compositions. The invention further provides multi-valent vaccines, which provide protective immunity when administered in an effective amount to animals susceptible to “shipping fever” or bovine respiratory disease.

First claim

Opening claim text (preview).

What is claimed is: 1. An intranasal vaccine comprising an attenuated Mannheimia haemolytica ( M. haemolytica ) A1 strain and an attenuated M. haemolytica A6 strain, which vaccine provides a safe and protective immune response in a bovine against both M. haemolytica strain A1 and M. haemolytica strain A6, or diseases caused by M. haemolytica strains A1 and A6. 2. The intranasal vaccine of claim 1 , wherein both the A1 and A6 strains contain nucleic acid deletions in their respective leukotoxin A (lktA) genes, which deletions have rendered the strains attenuated relative to the virulent parental strains A1 and A6 from which the attenuated strains A1 and A6 were produced. 3. The intranasal vaccine of claim 2 , consisting essentially of the attenuated strains. 4. The intranasal vaccine of claim 2 , further comprising an adjuvant. 5. The intranasal vaccine of claim 2 , wherein a safe and protective intranasal dose of the vaccine comprises from about 1.19×10 6 to 1.19×10 7 CFU of the attenuated A1 strain and from about 9.2×10 5 to 9.2×10 6 CFU of the attenuated A6 strain. 6. The intranasal vaccine of claim 2 , further comprising a pharmaceutically or veterinary acceptable vehicle, diluent or excipient and from about 1.19×10 6 to 1.19×10 7 CFU of the attenuated A1 strain and from about 9.2×10 5 to 9.2×10 6 CFU of the attenuated A6 strain. 7. The intranasal vaccine of claim 5 , further comprising an adjuvant. 8. The intranasal vaccine of claim 7 , wherein the adjuvant is inactivated bacteria, inactivated virus, fractions of inactivated bacteria, bacterial lipopolysaccharides, bacterial toxins, or derivatives or combinations thereof. 9. The intranasal vaccine of claim 2 , which provides a protective immune response in a bovine against an experimental challenge of about 2.4×10 9 CFU of virulent M. haemolytica strain A1. 10. The intranasal vaccine of claim 2 , further comprising at least one additional antigen associated with a bovine pathogen other than M. haemolytica. 11. A method of vaccinating an animal comprising administering at least one dose of the intranasal vaccine of claim 2 . 12. The method of claim 11 , wherein the animal is a bovine. 13. The method of claim 11 , wherein the bovine is a calf that is 28 days or older. 14. An immunological composition suitable for the prevention of bovine respiratory disease caused by M. haemolytica , comprising the vaccine of claim 2 , and further comprising an immunologically effective amount of attenuated Pasteurella multocida and Histophilus somni. 15. The composition of claim 14 , comprising from about 1.19×10 6 to 1.19×10 7 CFU of the attenuated A1 strain and from about 9.2×10 5 to 9.2×10 6 CFU of the attenuated A6 strain. 16. The composition of claim 14 , further comprising an adjuvant. 17. The composition of claim 16 , wherein the adjuvant is selected from inactivated bacteria, inactivated virus, fractions of inactivated bacteria, bacterial lipopolysaccharides, bacterial toxins, chitosan, derivatives and combinations thereof. 18. The composition of claim 17 , wherein the adjuvant is a chitosan derivative.

Assignees

Inventors

Classifications

  • Adaptation or attenuation of cells · CPC title

  • intranasal · CPC title

  • from Pasteurellaceae (F), e.g. Haemophilus influenza · CPC title

  • Antibacterial agents · CPC title

  • A61K39/102Primary

    {Pasteurellales, e.g. Actinobacillus}, Pasteurella; Haemophilus · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9675682B2 cover?
The present invention provides attenuated M. haemolitica strains that elicit an immune response in animal against M. haemolitica , compositions comprising said strains, methods of vaccination against M. haemolitica , and kits for use with such methods and compositions. The invention further provides multi-valent vaccines, which provide protective immunity when administered in an effective a…
Who is the assignee on this patent?
Merial Inc, Merial Inc
What technology area does this patent fall under?
Primary CPC classification A61K39/102. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).