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Novel vaccine compositions comprising immunostimulatory oligonucleotides

A vaccine composition, immunostimulatory technology, applied in the direction of drug combination, medical preparations containing active ingredients, microorganisms, etc., can solve problems such as toxicity or animal recurrence

Active Publication Date: 2018-03-20
ZOETIS SERVICE LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Numerous treatments have been described, but none are completely satisfactory, either due to the toxicity of the treatment itself or the tendency of animals to relapse

Method used

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  • Novel vaccine compositions comprising immunostimulatory oligonucleotides
  • Novel vaccine compositions comprising immunostimulatory oligonucleotides
  • Novel vaccine compositions comprising immunostimulatory oligonucleotides

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0087] The preparation of vaccine compositions comprising an oil phase is straightforward and requires the separation of an aqueous phase comprising the antigen, class P immunostimulatory oligonucleotides, and optionally a water-soluble emulsifier with an oil and optionally a fat-soluble emulsifier. The oil phase is mixed. The resulting mixture was emulsified.

[0088] Other components of the composition may include pharmaceutically acceptable excipients such as carriers, solvents and diluents, isotonic agents, buffers, stabilizers, preservatives, vasoconstrictors, antibacterial agents, antifungal agents agent and so on. Typical carriers, solvents and diluents include water, saline, dextrose, ethanol, glycerol, oils and the like. Representative isotonic agents include sodium chloride, dextrose, mannitol, sorbitol, lactose, and the like. Suitable stabilizers include gelatin, albumin, and the like.

[0089] As used herein, "pharmaceutically acceptable carrier" includes any a...

Embodiment 1

[0097] Example 1: Leishmania antigens

[0098] Fifty laboratory-bred male and female Beagle dogs were obtained from Marshall BioResources (NY), and 5 dogs were randomly assigned to each of the 10 groups (Table 1). The dogs were between 3 and 4 months old at the time of the first injection. Three injections were administered at 21 day intervals; injection sites were observed, and blood samples were collected at indicated intervals for testing. P-CpG of SEQ ID NO:8 was used in this study.

[0099] Table 1: Experimental design for Leishmania antigen studies in dogs

[0100]

[0101]

[0102] CpG-P oligonucleotides

[0103] Q-Quil A

[0104] C-cholesterol

[0105] MDP-muramoyl dipeptide

[0106] FML-fucose-mannose ligand

[0107] E-SA- -SA

[0108] PMBCs were isolated on day 1, day 7, day 28 and day 49. Isolated PBMC were cultured in (medium) and treated with FML (20 μg / ml), LICE (Leishmania infantum (Leishmania Infantum) crude extract, 17.5 μg / ml) and ConA (con...

Embodiment 2

[0115] Example 2: EHV antigens

[0116] animal

[0117] Cross-bred males and mares aged 11-12 months were divided into treatment groups containing 5 horses each. Horses were maintained in outdoor facilities during the vaccination phase. Because nearly all horses are exposed to EHV in early life, horses are not truly untreated. Use SN titers to select animals with low titers, however, previous exposures may affect interpretation of test results. Conventionally killed EHV-1 was used as antigen in this study.

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PUM

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Abstract

The present invention provides a vaccine composition comprising an antigenic component and an adjuvant component, wherein the adjuvant component comprises a P class immunostimulatory oligonucleotide and a combination of saponins and sterols; or comprises oil and optionally An oily phase of one or more emulsifiers, said oily phase comprising 2-20% v / v of said vaccine composition, wherein said antigenic component is an EHV antigen or a Leishmania antigen.

Description

technical field [0001] The present invention relates to novel adjuvants for enhancing the immune response to Leishmania and equine virus vaccines. Background technique [0002] Equine herpesviruses are major equine pathogens responsible for virus-induced abortions, neurological disorders such as paresis, upper respiratory tract infections, and neonatal foal disease (NFD). NFD is caused by transplacental infection of near-term fetuses who are born weak, with severe respiratory disease and some with jaundice due to liver infection caused by EHV-1. These animals usually die within a few days of birth. Equine rhinopneumonia virus (EHV-4) is a major cause of acute respiratory disease ("rhinopneumonia") and infects most horses during their first two years of life. Rhinopneumonia is characterized by fever, anorexia, and a profuse serous nasal discharge that later becomes mucopurulent. In rare cases, EHV4 infection has caused miscarriage in pregnant mares. Furthermore, EHV1 and ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K39/39A61K39/008A61K39/27
CPCA61K39/008A61K39/27A61K39/39A61K2039/55561A61K2039/55577C12N2710/16034A61K2039/55566C12N2710/16734A61K39/12A61P31/00A61P31/22A61P33/00A61P33/02A61P37/04Y02A50/30
Inventor P·J·多明诺夫斯基S·K·雷L·M·斯莱C·P·库克D·姆旺吉D·L·福斯R·L·克雷布斯
Owner ZOETIS SERVICE LLC