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公开(公告)号:EP3231868A4
公开(公告)日:2018-05-23
申请号:EP15867235
申请日:2015-09-07
发明人: WU JUN , SUN PENG , LIU BO , CHANG SHAOHONG , GONG XIN , WANG HENGLIANG , ZHU LI , PAN CHAO , FENG ERLING
CPC分类号: A61K39/0275 , A61K48/00 , A61K2039/521 , A61K2039/523 , C12N9/1051 , C12N9/93 , C12N15/11 , C12N15/63 , C12N15/74 , C12Y204/01 , C12Y600/00 , Y02A50/472 , Y02A50/482
摘要: The present invention discloses a Salmonella Paratyphi A with an O-antigen having an extended carbohydrate chain and uses thereof. The method comprises the following steps: inactivating an cld gene encoding an enzyme controlling chain length of O-antigen of a Salmonella paratyphi A strain to obtain a Salmonella paratyphi A with deletion of cld gene; allowing overexpression of cld LT2 gene encoding an enzyme controlling chain length of O-antigen of Salmonella typhimurium in Salmonella paratyphi A deficient in the cld gene encoding an enzyme controlling chain length of O-antigen, so as to extend carbohydrate chain length of O-antigen. Both of the Salmonella paratyphi A O-polysaccharide-recombinant fusion protein conjugate vaccines rCTB4573 3 -OPS Spty 50973 and rEPA4573-OPS Spty 50973 as prepared by using Salmonella Paratyphi A with an O-antigen having an extended carbohydrate chain can induce mice to generate specific antibodies against Salmonella paratyphi A, and their antibody titers are significantly improved.
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2.
公开(公告)号:EP3225690A4
公开(公告)日:2018-06-20
申请号:EP15862847
申请日:2015-09-01
发明人: WU JUN , PAN CHAO , SUN PENG , WANG HENGLIANG , LIU BO , PENG ZHEHUI , ZHU LI , CHANG SHAOHONG , GONG XIN , FENG ERLING , WANG BIN , ZENG MING
IPC分类号: C12N15/70 , A61K39/08 , A61K39/104 , A61K39/112 , A61P31/04 , C07K19/00 , C12N15/74
CPC分类号: A61K39/08 , A61K39/104 , C07K19/00 , C12N15/70 , C12N15/74 , Y02A50/472 , Y02A50/476 , Y02A50/482
摘要: The invention provided a method for preparing a bacterial polysaccharide-modified recombinant fusion protein and use of the bacterial polysaccharide-modified recombinant fusion protein. The method comprises: co-expressing a recombinant fusion protein and the Neisseria meningitidis O-oligosaccharyltransferase PglL in an O-antigen ligase gene-defective bacterium, and linking a polysaccharides endogenous or exogenous for the bacterium to the recombinant fusion protein by the O-oligosaccharyltransferase PglL, to obtain the bacterial polysaccharide-modified recombinant fusion protein. The protein can be used for preparing antibodies against bacterial polysaccharides and vaccines.
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