31 results about "Synthetic vaccine" patented technology

The present invention provides for novel immungens that are comprised of an activated polyhydroxypolymer backbone to which is attached 2 separate antigenic determinants. The 1st antigenic determinant includes a B-cell or CTL epitope and the 2nd antigenic determinant includes a T-helper epitope. In preferred embodiments, the antigenic determinants are derived from different molecules and species. Exemplary immunogens of the invention are constituted of a linear tresyl-activated dextran backbone to which is coupled B-cell or CTL epitopes of an antigen and to which is also coupled universal T-helper epitopes. Also disclosed are immunogenic compositions comprising the immunogens, methods of immunization and a method for identification of suitable immunogens of the invention.

The present invention relates to a constructed oligosaccharide cluster, optionally bonded to an immunogenic protein, that can be administered to a subject to induce an immune response for increasing production of 2G12 and / or used in assays as reactive sites for determining compounds that inactivate and / or bind the high-mannose oligosaccharide cluster. Compositions comprising these clusters, methods of using these clusters and compositions are disclosed.

This invention relates generally to identifying peptide sequences involved in antibody binding to any protein for synthesis of vaccine treatments. This novel method allows for a more manageable vaccine peptide discovery and specific generation of unique immunogenic peptides from self-tumor associated proteins and / or foreign proteins from infectious organisms for specific and / or enhanced expression only in the presence of the antibody.

The present invention provides synthetic vaccine delivery compositions based on polyester amide (PEA), polyester urethane (PEUR), and polyester urea (PEU) polymers for stimulating an immune response to a variety of pathogenic organisms and tumor cells in humans and other mammals. The vaccine delivery compositions are formulated as a liquid dispersion of polymer particles or molecules including class I or class II antigen peptides derived from organism or tumor cell proteins, which are taken up by antigen presenting cells of the mammal to induce an immune response in the mammal. Methods of inducing an immune response to the pathogenic organism or tumor cells in the invention compositions are also included.

Embodiments of the present invention include conserved-element vaccines and methods for designing and producing conserved-element vaccines. A conserved-element vaccine (“CEVac”) is a recombinant and / or synthetic vaccine that incorporates only highly conserved epitopes from an observed set of pathogen variants. The conserved epitopes are identified computationally by aligning biopolymer sequences, such as concatenated polypeptide sequences that together represent a pathogen proteome, corresponding to an observed set of pathogen variants, and computationally selecting conserved subsequences according to a number of subsequence-selection criteria. These subsequence-selection criteria may include a minimum conserved-subsequence length, a threshold frequency of occurrence of a particular monomer at each conserved, single-monomer position within a conserved subsequence, a threshold combined occurrence for a set of allowable variant monomers at a particular conserved, variable position within a conserved subsequence, and a maximum number of variable positions within a subsequence. A set of conserved subsequences identified according to the subsequence-selection criteria are then filtered to remove subsequences identical to, or too similar to, naturally-occurring host subsequences, and are then assembled into expression vectors for incorporation into microbial hosts for biosynthesis of a recombinant CEVac or assembled into one or more synthetic constructs for a synthetic CEVac.

The invention belongs to the field of biomedical engineering, and more specifically, the invention relates to a novel ultrasonic microbubble used as an immune adjuvant and a vaccine carrier. Ultrasonic microbubbles carrying vaccine antigens are synthesized by adhering vaccine antigens to the surface of the microbubbles and / or wrapping them in the microbubbles; when in use, the microbubbles carrying vaccine antigens act on the target tissue through the system and locally, and the target tissue is destroyed by ultrasonic waves. The microbubbles in the tissue area release the vaccine antigen material in a targeted manner and enhance the immune activity of the antigen. It is expected to be developed as a new type of immune adjuvant and vaccine carrier, especially for new adjuvants and carriers suitable for polypeptide vaccines, nucleic acid vaccines, virus and bacterial vaccines.

The invention discloses an A-type clostridium perfringens populus skin lipoid inactivated vaccine which is synthesized by taking populus skin lipoid as an aduvant and mixing A-type clostridium perfringens toxin subjected to inactivation and detoxication and the populus skin lipoid aduvant. The concrete method comprises the following steps: aseptically inoculating A-type clostridium perfringens in liver and gastric enzyme digestion soup, anaerobically culturing at 37 DEG C for 15-20h, selecting typical colonies to be inoculated on a blood inclined plane, and anaerobically culturing at 37 DEG C for 20-24h; then inoculating in the liver and gastric enzyme digestion soup according to a proportion of 1 percent of the total weight of a culture medium, culturing at a constant temperature of 35 DEG C for 7-8h, centrifuging to obtain the toxin, adding formaldehyde which is 0.3-0.5 percent of the total weight of the toxin, and carrying out inactivation and detoxication at 37 DEG C for 5d; mixing the toxin subjected to inactivation and detoxication with the populus skin lipoid aduvant according to the weight ratio of 4:1 and stirring at high speed to synthesize the vaccine. The A-type clostridium perfringens populus skin lipoid inactivated vaccine has long immunity time, no vaccination reaction after being injected and small stress.

The present invention relates to the total synthesis of saccharide structures contained in the capsular polysaccharide of Streptococcus pneumoniae type 1, to glycoconjugates containing said saccharide structures obtained by total synthesis and to use of such glycoconjugates and pharmaceutical compositions thereof in the immunization against diseases associated with bacteria containing said saccharide structures in their capsular polysaccharide, and more specifically associated with Streptococcus pneumoniae.

An outer membrane vaccine for preventing the infection of typhoid bacillus and paratyphoid bacillus A and B is disclosed. Its preparing process includes such steps as culturing said bacilli in culture liquid, getting their thallus, and preparing vaccine.

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.

The invention provides a GMP compatible method to chemically synthesize proteins which may be advantageously used in compositions for vaccination that are free of biological contaminants. The method uses conventional synthesis of peptides and linking these to yield synthetic proteins that preferably comprise all T cell epitopes for an antigen. Preferably an adjuvant is covalently attached to a synthetic protein to yield a fully synthetic vaccine. The invention is illustrated mainly by using HPV proteins directed immunity as a model.

The present invention provides a protein- and peptide-free conjugate comprising a synthetic carbohydrate and a carrier molecule, wherein the synthetic carbohydrate is a Streptococcus pneumoniae type 3 capsular polysaccharide related carbohydrate and the carrier molecule is a glycosphingolipid. Said conjugate and pharmaceutical composition thereof are useful for immunization against diseases associated with Streptococcus pneumoniae, and more specifically against diseases associated with Streptococcus pneumoniae type 3.

The present invention relates to a synthetic saccharide of general formula (I) that is related to Streptococcus pneumoniae serotype 2 capsular polysaccharide, a conjugate thereof and the use of said saccharide and conjugate for raising a protective immune response in a human and / or animal host. Furthermore, the synthetic saccharide of general formula (I) is useful as marker in immunological assays for detection of antibodies against Streptococcus pneumoniae type 2 bacteria.

The present invention provides a rapid qualitative and quantitative detection method for an oil adjuvant vaccine. The rapid qualitative and quantitative detection method comprises: demulsifying a foot-and-mouth disease synthetic peptide vaccine, and carrying out qualitative and quantitative detection on the demulsified antigen sample by using a competitive ELISA method, wherein the demulsifying method comprises: mixing a foot-and-mouth disease synthetic vaccine and a demulsifying agent, and layering to obtain a water phase antigen sample, the demulsifying agent comprises the mixture of an organic solvent and an acid, the organic solvent is one selected from acetonitrile, n-butanol, benzyl alcohol, butyl diethylene glycol and ethanol, and the acid is one selected from hydrochloric acid, acetic acid, formic acid and trifluoroacetic acid. According to the present invention, the demulsifying ability of the demulsifying method is strong, wherein the sample can be determined without the purification treatment so as to shorten the detection time; and the antigen concentration is subjected to qualitative and quantitative detection by using the competitive ELISA method, such that the slope of the obtained standard curve can be greater than the slope of the standard curve obtained through the conventional indirect competition method so as to substantially improve the detection sensitivity.