http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112018015237-A2

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K39-095
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7024
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-205
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7024
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 2017-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b93669a7d214cee6a41e94ca0a81e7b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d2756454f22b601839571154c898079
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e778585b6b5fc8c840eb504402610637
publicationDate 2018-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112018015237-A2
titleOfInvention modified hexa-acyl neisseria lps
abstract The present invention relates to a neisserial lps having a chemical fraction of the hexa-acylated lipid, wherein the chemical fraction of the hexa-acylated lipid is modified compared to the chemical fraction of the lipid to one of the hexa-acylated lipid. wild type wherein it comprises a palmitoleoyl instead of a lauryl secondary acyl chain at the non-reducing end of the lipid a chemical fraction. The invention further relates to mixtures of hexa-acylated lps with the corresponding penta-acylated lps, which does not have a glucosamine secondary acyl chain at the non-reducing end of the lipid a chemical fraction. The invention also relates to neisserial bacteria that have been genetically engineered to reduce expression of the endogenous lpxl1 gene and to introduce expression of a heterologous thermosensitive lpxp gene to produce the hexa and penta-acylated lps. By selecting the time and / or temperature at which the bacterium is proliferated, it is feasible to increase or decrease the amount of lipid to hexa-acylated structure relative to the penta-acylated structure, and thereby modulate the agonist activity of the bacterium. of the neisserial lps of the invention at the exact level of activity required for a particular immunotherapeutic approach.
priorityDate 2016-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.