US2022236284A1PendingUtilityA1

Therapeutically Triggering an Innate Immune Response in a Target Tissue

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Assignee: QU BIOLOGICS INCPriority: Apr 26, 2016Filed: Dec 6, 2021Published: Jul 28, 2022
Est. expiryApr 26, 2036(~9.8 yrs left)· nominal 20-yr term from priority
A61P 37/04C12Q 2600/156C12Q 1/6883A61K 2039/545A61K 2039/58A61K 2039/585A61K 39/0258A61K 2039/55594G01N 33/6869C12Q 1/6886C12Q 2600/158A61P 35/00A61P 29/00A61K 2039/577G01N 2800/50A61K 39/39C12Q 2600/106A61K 2039/55511A61K 39/092A61K 39/0266G01N 33/6863G01N 2333/065C12Q 2600/112A61K 2039/55555G01N 33/6866A61K 36/064A61K 39/0011A61K 35/74
52
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Claims

Abstract

The invention provides therapeutic compositions that present an artificial repertoire of mammalian pattern recognition receptor (PRR) agonists, so that the pattern of PRR agonists recapitulates a distinct portion of a PRR agonist signature of a mammalian pathogen. The artificial repertoire of PRR agonists may be formulated together in a therapeutic vehicle for combined presentation to an innate immune cell resident in a target tissue in a mammalian host, and the vehicle adapted to deliver the PRR agonists to the target tissue, so as to modulate an immune response.

Claims

exact text as granted — not AI-modified
1 - 8 . (canceled) 
     
     
         9 . The method according to  claim 36 , wherein the therapeutic vehicle further comprises one or more of: GMCSF, vitamin D, NOHA, alph1 antitrypsin, glutathione, an isoprenoid, or α-galactosylceramide. 
     
     
         10 - 19 . (canceled) 
     
     
         20 . The method according to  claim 36 , wherein therapeutic vehicle is administered at an administration site that is the skin or subcutaneous tissue. 
     
     
         21 - 24 . (canceled) 
     
     
         25 . The method according to  claim 36 , wherein the therapeutic vehicle is administered in a plurality of doses over a dosage duration, and the dosage duration is at least two weeks. 
     
     
         26 . The method according to  claim 25 , wherein the doses are administered subcutaneously every day, or every other day. 
     
     
         27 . (canceled) 
     
     
         28 . The method according to  claim 36 , wherein the patient is immunosuppressed or immunocompromised. 
     
     
         29 . The method according to  claim 36 , wherein the patient is a geriatric patient. 
     
     
         30 . The method according to  claim 36 , wherein the patient is a pediatric patient. 
     
     
         31 - 32 . (canceled) 
     
     
         33 . The method of  claim 36 , wherein the  Klebsiella  spp. is a  K. variicola  or  K. pneumonia  that is a pathogenic strain of  K. variicola  or  K. pneumonia.    
     
     
         34 - 35 . (canceled) 
     
     
         36 . A method of treating neutropenia in a human patient, comprising administering to the patient an effective amount of a therapeutic vehicle, comprising a whole killed or attenuated cell of a  Klebsiella  spp. 
     
     
         37 . The method of  claim 36 , wherein the neutropenia is caused by a myelosuppressive chemotherapy. 
     
     
         38 - 73 . (canceled)

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