US2016015799A1PendingUtilityA1

Recombinant antigens of the porcine circovirus 2 (pcv-2) for vaccine formulations and use thereof

Assignee: UNIV FED DE VIÇOSAPriority: Jan 25, 2013Filed: Oct 5, 2015Published: Jan 21, 2016
Est. expiryJan 25, 2033(~6.5 yrs left)· nominal 20-yr term from priority
A61P 31/20A61K 39/12C12N 2750/10034G01N 33/56983C07K 14/005G01N 2469/20C12N 2750/10023G01N 2333/015A61K 2039/55505G01N 2333/01A61K 2039/5258C12N 7/00
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Claims

Abstract

The present continuation-in-part of the Application BR 7 10 2013 001893 refers to the obtainment of the viral capsid recombinant antigen of the Porcine circovirus 2 (PCV-2) and modifications thereof, upon expression in prokaryotic system, recovery of virus-like particles (VLPs) and its use in vaccine formulations. The antigens and vaccine formulations can be used in the immunization of animals in control programs of the diseases associated with PCV-2 in conventional swine production systems and represent alternatives to vaccines available on the market.

Claims

exact text as granted — not AI-modified
1 . A recombinant antigen of the porcine circovirus 2 which is the SEQ ID NO: 02. 
     
     
         2 . A recombinant antigen, which comprises the product of the oligomerization of SEQ ID NO: 02 in the form of virus-like particles (VLPs) of the PCV-2. 
     
     
         3 . Vaccine formulations which comprise the antigen as defined in  claim 1 , associated with pharmaceutically acceptable adjuvants. 
     
     
         4 . Uses of the antigen as defined in  claim 1 , which is applied in the production of vaccine compounds. 
     
     
         5 . Use of the vaccine formulations defined in  claim 3 , which is for the control of diseases related to the PCV-2. 
     
     
         6 . Vaccine formulations which comprise the VLPs as defined in  claim 2  associated with pharmaceutically acceptable adjuvants. 
     
     
         7 . Uses of the antigen as defined in  claim 2  which is applied in the production of vaccine compounds. 
     
     
         8 . Use of the vaccine formulations as defined in  claim 6  which is for the control of diseases related to the PCV-2.

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