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44 results about "Synthetic Immunogens" patented technology

Novel immunogenic lipopeptides comprising t-helper and b-cell epitopes

The present invention provides synthetic immunogenic lipopeptide molecules comprising co-linear T-helper and B cell epitopes, and methods for their production and use in the generation of primary and secondary immune responses, and for the vaccination of animal subjects against particular antigens. More particularly, the present invention provides highly soluble lipopeptides wherein the lipid moiety is attached to the terminal side-chain group of an internal lysine or lysine analog, preferably to the terminal side-chain group of an internal diamino acid residue. Preferably the internal lysine or lysine analog is positioned between the T-helper epitope and the B cell epitope or within the T-helper epitope.
Owner:COUNCIL OF THE QUEENSLAND INST OF MEDICAL RES

Method for producing human antibodies with properties of agonist, antagonist, or inverse agonist

A method for obtaining agonist, antagonist and inverse agonist, to a given physiological receptor is disclosed. For the method, use is made of in silico design synthetic immunogens, which are caused to act in vitro on human lymphocyte-containing cell populations. A preferred receptor is human CD152, particularly the regions of CDRl, CDR2 and CDR3 that elicit antibodies serving as antagonist, inverse agonist and agonist, respectively. Also provided is a method in the treatment of human peripheral lymphocytes for use in the screening of CD152 ligands that yield pharmacological effects.
Owner:HUMORIGIN BIOTECH CORP

Immunogenic lipopeptides comprising T-helper and cytotoxic T lymphocyte (CTL) epitopes

The present invention provides synthetic immunogenic lipopeptide molecules comprising co-linear T-helper and CTL epitopes, and methods for their production and use in the generation of primary and secondary immune responses, and for the vaccination of animal subjects against particular CTL epitopes. More particularly, the present invention provides highly soluble lipopeptides wherein the lipid moiety is attached to the terminal side-chain group of an internal lysine or lysine analog, preferably to the terminal side-chain group of an internal diamino acid residue. Preferably the internal lysine or lysine analog is positioned between the T-helper epitope and the CTL epitope.
Owner:COUNCIL OF THE QUEENSLAND INST OF MEDICAL RES

Pyrethroid hapten design based on computer molecular simulation technique and application

The invention relates to pyrethroid hapten design based on a computer molecular simulation technique and an application, which belongs to the technical field of pyrethroid pesticide detection. Six kinds of available hapten are designed by using the pyrethroid hapten design. Gaussian software is utilized to calculate charge distribution of the hapten and a target object, and Discovery Studio 2.5 software is utilized to establish spatial conformation of the hapten and the target object. By comparison, the hapten with the highest degree of structure similarity is selected as immune hapten (hapten 1), the hapten is predicted to generate a good immune effect, and the hapten with higher structure difference is selected as coated hapten (hapten 5). The computer molecular simulation software is successfully used by the method to design the hapten of a pyrethroid pesticide; a mass selection antibody which is used for identifying the pyrethroid pesticide is prepared through synthesis of immunogen and immunity, serum screening, fusion, screening and acrylics; the method is proven to have strong predictive ability, and time and funds are saved; and a new method is provided for later analyzing and researching immunology.
Owner:JIANGNAN UNIV

Method for producing human antibodies to human CD152 with properties of agonist, antagonist, or inverse agonist

A method for obtaining agonist, antagonist and inverse agonist, to a given physiological receptor is disclosed. For the method, use is made of in silico design synthetic immunogens, which are caused to act in vitro on human lymphocyte-containing cell populations. A preferred receptor is human CD152, particularly the regions of CDR1, CDR2 and CDR3 that elicit antibodies serving as antagonist, inverse agonist and agonist, respectively. Also provided is a method in the treatment of human peripheral lymphocytes for use in the screening of CD152 ligands that yield pharmacological effects.
Owner:HUMORIGIN BIOTECH CORP

Synthetic immunogen useful for generating long lasting immunity and protection against pathogens

InactiveUS20130183377A1Induced proliferationGenerating long lasting protective immunityAntibacterial agentsPowder deliverySynthetic ImmunogensTrypanosomiasis
The present invention relates to a synthetic immunogen represented by the general formula 1, useful for generating long lasting protective immunity against various intracellular pathogens which are the causative agents of tuberculosis, leishmaniasis, AIDS, trypanosomiasis, malaria and also allergy, cancer and a process for the preparation thereof. The developed immunogen is able to circumvent HLA restriction in humans and livestock. The invention further relates to a vaccine comprising the said immunogen for generating enduring protective immunity against various diseases. The said vaccine is targeted against intracellular pathogens, more particularly the pathogen M. tuberculosis in this case. In the present invention, promiscuous peptides of M. tuberculosis are conjugated to TLR ligands especially; Pam2Cys to target them mainly to dendritic cells and therefore elicit long-lasting protective immunity. (The formula (I) should be inserted here) General formula (I) wherein, X1=a promiscuous CD4 T helper epitope selected from SEQ ID No. 1 to 98 OR nil; X2=a promiscuous CD8 T cytotoxic epitope selected from SEQ ID No. 99 to 103 OR nil; when X1=nil; X2=SEQ ID No. 99 to 103 and when X2=nil; X1=SEQ ID No. 1 to 98; Y=Lysine; and S=Serine.
Owner:COUNCIL OF SCI & IND RES +1

Novel immunogenic lipopeptides comprising t-helper and cytotoxic t lymphocyte (ctl) epitopes

The present invention provides synthetic immunogenic lipopeptide molecules comprising co-linear T-helper and CTL epitopes, and methods for their production and use in the generation of primary and secondary immune responses, and for the vaccination of animal subjects against particular CTL epitopes. More particularly, the present invention provides highly soluble lipopeptides wherein the lipid moiety is attached to the terminal side-chain group of an internal lysine or lysine analog, preferably to the terminal side-chain group of an internal diamino acid residue. Preferably the internal lysine or lysine analog is positioned between the T-helper epitope and the CTL epitope.
Owner:COUNCIL OF THE QUEENSLAND INST OF MEDICAL RES

Stabilized synthetic immunogen delivery system

ActiveUS8084015B2Effectively upregulating immune responseEasy to demonstrateAntimycoticsImpression capsSynthetic ImmunogensParticulates
The present invention provides an immunostimulatory complex specifically adapted to act as adjuvant and as a peptide immunogen stabilizer. The immunostimulatory complex comprises a CpG oligonucleotide and a biologically active peptide immunogen. The immunostimulatory complex is particulate and can efficiently present peptide immunogens to the cells of the immune system to produce an immune response. The immunostimulatory complex may be formulated as a suspension for parenteral administration. The immunostimulatory complex may also be formulated in the form of w / o-emulsions, as a suspension in combination with a mineral salt suspension or with an in-situ gelling polymer for the efficient delivery of an immunogen to the cells of the immune system of a subject following parenteral administration, to produce an immune response which may also be a protective immune response.
Owner:UNITED BIOMEDICAL INC

Polypeptide GPR5 and application thereof to promoting of hepatocyte proliferation and inhibiting of hepatocyte apoptosis

The invention discloses polypeptide GPR5 and application thereof to promoting of hepatocyte proliferation and inhibiting of hepatocyte apoptosis. The invention discloses polypeptide and application thereof to promoting of hepatocyte proliferation and / or inhibiting of hepatocyte apoptosis. According to the polypeptide capable of promoting hepatocyte proliferation and / or inhibiting hepatocyte apoptosis, compared with an amino acid sequence shown in SEQ ID NO:1, the amino acid sequence of the polypeptide has 3 / 5 or above sequence consistency, the polypeptide length is 5 amino acids, the polypeptide has the advantages of being small in molecular weight, easy to synthesize, low in immunogenicity and the like, and therefore the polypeptide has broad application prospects in treatment of hepatopathy.
Owner:LINK HEALTH GRP

Monoclonal antibody hybridoma cell strain YH4 resisting furaltadone metabolite AMOZ and application thereof

Belonging to the technical field of food safety immunodetection, the invention discloses a monoclonal antibody hybridoma cell strain YH4 resisting furaltadone metabolite AMOZ and application thereof. The hybridoma cell strain YH4 is preserved in the China General Microbiological Culture Collection Center, and the preservation number is CGMCC No.12017. The monoclonal antibody resisting furaltadone metabolite AMOZ is secreted by the hybridoma cell strain YH4. The monoclonal antibody secreted by the cell strain YH4 has good specificity (an IC50 value of 0.2microgram / L) to furaltadone metabolite AMOZ, has good detection sensitivity and affinity, and can be used for specific detection of anti-furaltadone metabolite AMOZ in food safety. The invention also provides a new method for synthesis of furaltadone metabolite AMOZ immunogen, the synthesis steps of hapten are more simplified and effective, thus providing an immunogen synthesis idea and method for future research of people.
Owner:JIANGNAN UNIV

Synthetic immunogens for prophylaxis or treatment of tuberculosis

Compositions comprising a nucleic acid molecule that encodes TB esat-6 proteins are disclosed. Methods of inducing an immune response against TB an individual are disclosed. Method of treating an individual who has been diagnosed with TB are disclosed. Method of preventing TB infection in an individual are disclosed.
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA

Estriol-specificity-resistant monoclonal antibody hybridoma cell strain NaN-2 and application thereof

The invention provides an estriol-specificity-resistant monoclonal antibody hybridoma cell strain NaN-2 and application thereof and belongs to the technical field of food safety immune detection. The estriol-specificity-resistant monoclonal antibody hybridoma cell strain NaN-2 is preserved in General Microbiology Center, Microbial Preservation Management Committee, China, and the preservation number is CGMCC No. 12016. An estriol-specificity-resistant monoclonal antibody is generated by secretion of the hybridoma cell strain NaN-2. The monoclonal antibody secreted by the cell strain has good specificity to estriol (the IC 50 value is 0.25 ng / mL) and can be used for estriol specificity detection in food safety. The obtained estriol-resistant monoclonal antibody cell strain has good detection sensitivity and appetency to estriol, a novel method for synthesizing estriol immunogen is further provided, the synthesis step of hapten is more simplified and effective, and a thought and method for synthesizing immunogen are provided for people to conduct research in the future.
Owner:深圳重链生物科技有限公司

Synthetic vaccine for tick control

This invention is related to the field of immunology of protein biotechnology and particularly to the construction of synthetic immunogens which result, where inoculated, in the production by cattle of an immune response capable of lesion to the ticks feeding on the inoculated bovines, reducing their number, their weight and their reproductive capacity to such an extent that the constructed immunogen can be used as an effective vaccine for tick control on bovines. The technical object of the invention consists of the design and construction of two synthetic immunogens constituted of a continuous and defined sequence with forty-three (43) amino acids, found in different positions in the sequence of protein Bm86, their polymerization with cysteine in the N-terminal and in the C-terminal, the medicamentous composition based on said peptide(s) and the synthetic vaccine obtained thereby.
Owner:FUNDACAO UNIVE FEDERAL DE VICOSA +1

Method for producing human antibodies with properties of agonist, antagonist, or inverse agonist

A method for obtaining agonist, antagonist and inverse agonist, to a given physiological receptor is disclosed. For the method, use is made of in silico design synthetic immunogens, which are caused to act in vitro on human lymphocyte-containing cell populations. A preferred receptor is human CD152, particularly the regions of CDR1, CDR2 and CDR3 that elicit antibodies serving as antagonist, inverse agonist and agonist, respectively. Also provided is a method in the treatment of human peripheral lymphocytes for use in the screening of CD152 ligands that yield pharmacological effects.
Owner:HUMORIGIN BIOTECH CORP

Polypeptide CAK18N and application thereof to promotion of regeneration and inhibition of liver apoptosis

The invention relates to polypeptide CAK18N and application thereof to promotion of regeneration and inhibition of liver apoptosis. The invention discloses polypeptide and application thereof of promotion of hepatic cell proliferation and / or inhibition of liver apoptosis. In the polypeptide capable of promoting hepatic cell proliferation and / or inhibiting liver apoptosis, the amino acid sequence has sequence consistency of more than 16 / 18 through comparison with the amino acid sequence as shown in SEQ ID NO:1, the length of the polypeptide is 18 pieces of amino acid, and the polypeptide has the advantages of small molecular weight, easiness in synthesis, low immunogenicity and the like, so the polypeptide provided by the invention has wide application prospect in liver disease treatment.
Owner:LINK HEALTH GRP

Application of FGF-2 derived polypeptide to preparation of medicines for promoting cartilage repairing and/or treating degenerative arthritis

The invention discloses an application of FGF-2 derived polypeptide to preparation of medicines for promoting cartilage repairing and / or treating degenerative arthritis. The FGF-2 derived polypeptideis polypeptide as shown in SEQID NO:1 or polypeptide as shown in SEQID NO:2. Peptide PDG6 and KED7 are from FGF-2, cartilage can be notably promoted to regenerate, and the FGF-2 derived polypeptide has favorable treatment effects on degenerative arthritis, besides, is easy to synthetize and low in immunogenicity, and has wide application prospects in treatment of cartilage injury and degenerativearthritis.
Owner:LINK HEALTH GRP

IKK beta-targeted short peptide and application thereof in inflammatory diseases

The invention belongs to the field of biological medicines, and particularly relates to an IKK beta-targeted short peptide and application thereof in inflammatory diseases. In order to provide a moreeffective treatment means for inhibiting inflammatory reaction, the invention provides the IKK beta-targeted short peptide. The short peptide comprises an N-terminal amino acid 46-60 region derived from I kappa B kinase binding protein IKIP, and the N terminal of the short peptide is fused with a cell-penetrating peptide and has a polypeptide marker. The short peptide can target IKK beta and inhibit combination of IKK beta and IKK gamma, thus, formation of an IKK complex is inhibited, expression of inflammatory cytokines TNF-alpha and IL-6 is reduced, and inflammatory reaction is inhibited. Ananimal model shows that the short peptide can effectively treat arthritis and inflammatory enteritis. Compared with full-length proteins, the short peptide has the advantages of small molecular weight, easiness in synthesis, weak immunogenicity and relatively weak side effects; and the cell-penetrating peptide has better absorption, and the polypeptide marker is easy to track and observe, and thus, a reference is provided for clinically treating the inflammatory diseases.
Owner:SHANDONG UNIV

Synthetic Immunogens For Prophylaxis Or Treatment Of Tuberculosis

Compositions comprising a nucleic acid molecule that encodes TB esat-6 proteins are disclosed. Methods of inducing an immune response against TB an individual are disclosed. Method of treating an individual who has been diagnosed with TB are disclosed. Method of preventing TB infection in an individual are disclosed.
Owner:THE TRUSTEES OF THE UNIV OF PENNSYLVANIA

Application of polypeptide in preparing medicine for treating pancreatitis and medicine containing polypeptide

The invention discloses application of an MEPE-derived polypeptide in preparing a medicine for treating pancreatitis and a medicine containing the MEPE-derived polypeptide. The MEPE-derived polypeptide is: a) a polypeptide represented by SEQ ID NO:1; or b) a polypeptide composed of amino acids at positions 5-19 in the amino acid sequence of the polypeptide represented by SEQ ID NO:1; or c) a cyclic peptide obtained by cyclization by adding Cys respectively to the N-terminal and C-terminal of the polypeptide composed of the amino acids at positions 5-19 in the amino acid sequence of the polypeptide represented by SEQ ID NO:1. The polypeptide provided by the invention has small molecular weight, is easy to synthesize, has low immunogenicity, has a good therapeutic effect on acute pancreatitis, can be used as a new type of medicine for acute pancreatitis, and has broad application prospects.
Owner:LINK HEALTH GRP

Pyrethroid hapten design based on computer molecular simulation technique and application

The invention relates to pyrethroid hapten design based on a computer molecular simulation technique and an application, which belongs to the technical field of pyrethroid pesticide detection. Six kinds of available hapten are designed by using the pyrethroid hapten design. Gaussian software is utilized to calculate charge distribution of the hapten and a target object, and Discovery Studio 2.5 software is utilized to establish spatial conformation of the hapten and the target object. By comparison, the hapten with the highest degree of structure similarity is selected as immune hapten (hapten 1), the hapten is predicted to generate a good immune effect, and the hapten with higher structure difference is selected as coated hapten (hapten 5). The computer molecular simulation software is successfully used by the method to design the hapten of a pyrethroid pesticide; a mass selection antibody which is used for identifying the pyrethroid pesticide is prepared through synthesis of immunogen and immunity, serum screening, fusion, screening and acrylics; the method is proven to have strong predictive ability, and time and funds are saved; and a new method is provided for later analyzing and researching immunology.
Owner:JIANGNAN UNIV

Method of manufacturing human antibody possessing bioreceptor synergist, antagonist and/or inverse synergist

A method for developing the synergist, antagon and reverse synergist of a particular bioreceptor includes using computer to design and synthesize the immunogen and externally acting on human lymphocyte cluster. Said receptor is human CD 152, especially the CDR1, CDR2 and CDR3 regions able to respectively trigger the antibody to play the role of synergist, antagon and reverse synergist. A method for determining their pharmacologic efficacy is also disclosed.
Owner:金立德 +1

Methods for polymering haptens into immunogens

The present invention discloses methods for polymerizing non-immunogenic haptens into immunogens, which then can be used to stimulate anti-hapten antibody production in animals. Specifically, haptens with amine and / or carboxylic groups are polymerized into macromolecules by using cross-linking reagents, and the derived haptenic polymers are used to immunize animals for the production of anti-hapten antibodies.
Owner:NATIONAL TAIWAN NORMAL UNIVERSITY

Polypeptide for promoting liver cell proliferation and/or inhibiting liver cell apoptosis and application thereof

The invention relates to a polypeptide and application thereof, in particular to a polypeptide for promoting liver cell proliferation and / or inhibiting liver cell apoptosis and application thereof. The amino acid sequence of the polypeptide for promoting liver cell proliferation and / or inhibiting liver cell apoptosis is selected from at least one of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5 and SEQ ID NO: 6. The polypeptide disclosed by the invention has the activity of promoting liver cell proliferation and / or inhibiting liver cell apoptosis, which is equivalent to or better than that of HIP / PAP, and has the advantages of small molecular weight, easiness in synthesis, low immunogenicity and the like, so that the polypeptide disclosed by the invention has a wide application prospect.
Owner:LINK HEALTH GRP

Polypeptide-antigen conjugates with non-natural amino acids

Methods for the production of immunogenic compositions containing a non-natural amino acid are disclosed. The non-natural amino acid can be a site for attachment of antigens, such as bacterial capsular polysaccharides, to make immunogenic conjugates. Bio-orthogonal attachment chemistry incorporated into the non-natural amino acids allows for more efficient and potent antigen presentation to the immune system, simplified purification, and more well-defined structure of these semi-synthetic immunogens.
Owner:VAXCYTE INC
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