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Truncated LHRH formulations

A domain, lipopeptide technology applied in the field of truncated LHRH formulations

Inactive Publication Date: 2007-12-05
昆士兰医学研究所理事会(QIMR)
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It should be recognized that these types of epitopes may vary widely

Method used

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  • Truncated LHRH formulations
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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0077] Each group of dogs received a total of 5n moles of a mixed peptide consisting of P25, P35 and P62 coupled to LHRH(2-10) as the first dose. As a second and third dose, one group of dogs received the same vaccine, while a second group received a vaccine consisting only of P25 coupled to LHRH(6-10). Dogs received three doses of the vaccine at 0, 4, and 14 weeks.

[0078] Vaccine preparation: 1 to 1.5 mg of each peptide was weighed and dissolved in 100 ul of 4M urea. Solutions corresponding to 1.7 nmoles of each peptide were mixed and diluted with isotonic saline to the prescribed dose volume for injection (1 ml per dose). Add 150ug of Iscomatrix to each dose  (CSL, Melbourne, Australia) as an adjuvant. The vaccine is given to the dog on the back of the neck.

[0079] The measured antibody titers are shown in Figure 1. Simultaneous testosterone and progesterone levels are shown in Figure 2 and Figure 3, respectively.

Embodiment 2

[0081] Vaccination regimen:

[0082] The Beagle / foxhounds were divided into three groups. One group (12 dogs) received three doses of 5n molar total peptide consisting of a mixture of p25, p35 and p62 peptides coupled to LHRH (6-10).

[0083] A second group (6 dogs) received three doses of 5n molar total peptide consisting of a mixture of p25, p35 and p62 peptides coupled to LHRH (2-10).

[0084] A third group (6 dogs) received three doses of 5n molar total peptide consisting of a mixture of p25, p35 and p62 peptides coupled to LHRH (2-10) as the first dose. For the second and third doses, the vaccine consisted of a mixture of the same peptides conjugated to LHRH(6-10).

[0085] Dogs received three doses of the vaccine at 0, 4, and 14 weeks.

[0086] vaccine preparation

[0087] Weigh 1 to 1.5 mg of each peptide and dissolve in 100 ul of 4M urea respectively. Solutions corresponding to 1.7 nmoles of each peptide were mixed and diluted with isotonic saline to the prescribe...

Embodiment 3

[0091] Vaccination regimen:

[0092]Divide the Beagles / Foxhounds into two groups. The first group (15 dogs) received three doses of 35n molar total peptide consisting of a mixture of p4, p10, p24, p25, p27, p35 and p62 peptides coupled to LHRH (6-10).

[0093] A second group (15 dogs) received three doses of 35n molar total peptide consisting of a mixture of p4, p10, p24, p25, p27, p35 and p62 peptides coupled to LHRH (4-10).

[0094] Dogs received three doses of the vaccine at 0, 4, and 14 weeks.

[0095] Vaccine preparation:

[0096] Weigh 1 to 1.5 mg of each peptide and dissolve in 100 ul of 4M urea respectively. Solutions corresponding to 5 nmoles of each peptide were mixed and diluted with isotonic saline to the prescribed dose volume for injection (1 ml per dose). Add 150ug of Iscomatrix to each dose  (CSL, Melbourne, Australia) as an adjuvant. The vaccine is given to the dog on the back of the neck.

[0097] The experimental results are shown in Figure 11 to Fig...

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Abstract

The present invention provides a peptide useful for raising an antiLHRH response in an animal. The peptide comprises a first and second region, the first region consisting of a sequence of less than 60 amino acids which comprises at least one T helper cell epitope and the second region consisting of the sequence SYGLRPG.

Description

field of invention [0001] The present invention relates to peptides comprising truncated forms of LHRH and T helper epitopes. These formulations can be used to increase antibodies against LHRH in animals. Background of the invention [0002] Any peptide capable of inducing an effective antibody response must contain a specific sequence of amino acids, known as an epitope, that is recognized by the immune system. Especially during an antibody response, epitopes need to be recognized by specific immunoglobulin (Ig) receptors on the surface of B lymphocytes. These cells eventually differentiate into plasma cells, which are able to produce antibodies specific for this epitope. In addition to these B-cell epitopes, the immunogen must also contain epitopes that are presented by antigen-presenting cells (APCs) to specific receptors present on helper T lymphocytes, which are essential for the differentiation of B cells into antibody-producing cells. desired signal is required. ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K14/59A61K38/24A61P15/16A61P15/18
CPCC07K14/59A61K39/0006C07K2319/00C07K7/08A61K38/00C07K7/23A61K2039/6018A61P15/16A61P15/18A61P5/10A61K38/24
Inventor 戴维·查尔斯·杰克逊约翰·沃克曾伟光
Owner 昆士兰医学研究所理事会(QIMR)
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