http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20220148550-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-4713
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-00
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filingDate 2021-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73f38bc7fcf14094ca308a761e742fe5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28ee64ce8414af15b4a9b05d7a42278f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e88bcc25a0750644130b8eba24106c1e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1b5e841b1d620adf4d79bf770526d73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_534f118d66dbd7b5170c2f61098d8870
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_105b417c0fc3684477348c42e97a93da
publicationDate 2022-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20220148550-A
titleOfInvention Composition for treating lupus disease containing CRIF1 as an active ingredient
abstract It relates to a composition for treating lupus disease comprising Crif1 as an active ingredient, wherein the deficiency of Crif1 in the B cells of the present invention results in the development of lupus disease, and the deficiency of Crif1 in the B cells is IgG, IgG2c and IgG3 and each antibody It was confirmed to increase the formation, increase the expression of genes associated with inflammation, and increase the number of dysfunctional mitochondria. In addition, it was confirmed that the deficiency of Crif1 in B cells increased the activity of inflammation-related B cells and follicular helper T cells, and increased the amount of inflammation-related cytokines IL-6 and IL-17. It was confirmed that the disease was improved and the amount of anti-dsDNA IgG antibody decreased.
priorityDate 2021-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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