US2023115331A1PendingUtilityA1

Glycotargeting therapeutics

Assignee: ECOLE POLYTECHNIQUE FED LAUSANNE EPFLPriority: Feb 21, 2014Filed: Jul 1, 2022Published: Apr 13, 2023
Est. expiryFeb 21, 2034(~7.6 yrs left)· nominal 20-yr term from priority
C07K 2317/24A61K 38/00A61K 38/164A61K 47/549A61K 38/2013A61K 38/08C07K 2317/21C07K 14/77C07K 16/241A61K 39/0002A61K 2039/6087A61K 38/37A61K 38/1709A61K 2039/60A61K 38/28A61K 39/35A61K 39/0008A61K 39/001C07K 16/2848A61K 39/0005C07K 2317/55A61K 38/38A61K 2039/577C07K 2319/01A61K 47/64C07K 14/07
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Claims

Abstract

Several embodiments of the present disclosure relate to glycotargeting therapeutics that are useful in the treatment of transplant rejection, autoimmune disease, food allergy, and immune response against a therapeutic agent. In several embodiments, the compositions are configured to target the liver and deliver antigens to which tolerance is desired. Methods and uses of the compositions for induction of immune tolerance are also disclosed herein.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A compound for the induction of antigen-specific immune tolerance in a subject, the compound comprising:
 an peptide to which tolerance is desired;
 wherein the peptide to which tolerance is desired, when presented alone to the subject is capable of inducing an unwanted immune response in the subject; 
   a polymeric linker comprising:
 a copolymer or a random copolymer, wherein the copolymer or random copolymer comprises a first methacrylate unit and a second methacrylate unit, the first methacrylate unit comprising a first ethylacetamido functionality and the second methacrylate unit comprising a second ethylacetamido functionality; 
 wherein the second ethylacetamido functionality is conjugated to an aliphatic group, an alcohol, or an aliphatic alcohol; 
 wherein the polymeric linker is bonded to the peptide to which tolerance is desired via a disulfide bond or a disulfanyl ethyl ester, 
 wherein the disulfide bond or the disulfanyl ethyl ester are each configured to be cleaved upon administration of the compound to the subject and to release the peptide to which tolerance is desired from the polymeric linker; and 
   a liver-targeting moiety;
 wherein the liver-targeting moiety comprises a galactosylating or glucosylating moiety; 
 wherein the liver-targeting moiety is bonded to the polymeric linker through the first ethylacetamido functionality.

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