Treatment of bacterial infections

• US 6,310,043 B1
• Filed: 05/24/1999
• Issued: 10/30/2001
• Est. Priority Date: 08/07/1998
• Status: Expired due to Fees

• Current Assignee: The Governors of the University of Alberta (University of Alberta)
• Original Assignee: The Governors of the University of Alberta (University of Alberta)
• Inventors: Armstrong, Glen, Ling, Hong, Bundle, David R., Kitov, Pavel, Read, Randy J.
• Primary Examiner(s): FONDA, KATHLEEN KAHLER
• Application Number:
  US09/317,290
• Time in Patent Office: 890 Days
• Field of Search: 514/25, 514/53, 514/54, 514/61, 435/34, 424/DIG.16
• US Class Current: 514/25
• CPC Class Codes: A61K 47/549 Sugars, nucleosides, nucleotides or nucleic acids
• CPC Class Codes: A61K 47/59 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
• CPC Class Codes: C07H 15/04 attached to an oxygen atom of the saccharide radical
• CPC Class Codes: C07H 3/04 Disaccharides
• CPC Class Codes: C07H 3/06 Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
• CPC Class Codes: Y10S 424/16 Dendrimers and dendritic polymers

Abstract

Compounds which bind to toxins associated with enteric bacterial infection, compositions including the compounds, methods for the neutralization of toxins in a patient, and methods for the diagnosis of bacterial and viral infections are disclosed. Toxins which can be bound by the compounds include pentameric toxins, for example SLTs, such as those from salmonella, camylobacter and other bacteria, verotoxins from E. coli, cholera toxin, clostridium difficile toxins A and B, bacterial pili from enteropathogenic E. coli (EPEC) and enterotoxigenic E. coli (ETEC) and viral lectins such as viral hemagglutinins. The compounds include a core molecule bound to a plurality of linker arms, which in turn are bound to a plurality of bridging moieties, which in turn are bound to at least one, and preferably, two or more ligands which bind to the toxin. The presence of a plurality of bridged dimers of the ligands is responsible for the increased binding affinity of the compounds relative to the ligands themselves. In one embodiment, the compounds, when administered in a timely fashion to a patient suffering from enteric E. coli infection, inhibit progression of this infection into hemolytic uremic syndrome (HUS).

Claims

1. A compound of the following structure:

2. The compound of claim 1 wherein the multifunctional compound is selected from the group consisting of monosaccharides, oligosaccharides, aldaric acids, amino acids, peptides, acrylamides, cyclodextrins, phthalocyanins and polyhydroxy alkanes.

3. The compound of claim 1 wherein at least one of the linker arms is selected from the group consisting of polymethylene, aryl groups, aralkyl groups alkaryl groups, alkylcycloalkanes, polyalkylene glycols, alkyl diamines, alkyl thio amines, and alkyl dithiols.

4. The compound of claim 1 wherein the bridging moieties include at least one functional group selected from the group consisting of carbamoyl, amide, carboxylic acid, hydroxy, thiol, amine, aldehyde, ketone, thioacid, thioester, thiourea, sulfonic acid, and phosphoric acid.

5. The compound of claim 1 wherein at least one of the ligands is a dimer or trimer including a saccharide selected from the group consisting of α

Gal(1→

4)β

Gal, α

Gal(1→

4)β

Gal(1→

4)β

GlcNAc and α

Gal(1→

4)β

Gal(1→

4)β

Glc., wherein the aglycon of the terminal reducing saccharide is alkyl, aryl, aralkyl, alkaryl, allyl or the corresponding thio analogues.

6. The compound of claim 1 wherein the number of linker arms is between 3 and 20.

7. The compound of claim 1, further comprising a pharmaceutically acceptable carrier for administration to a patient.

8. The compound of claim 1 wherein the linker is designed to bridge the spacing between the binding sites on proximal lectin subunits or proximal lectin molecules in a toxin including those moieties.

9. A method for treating a bacterial infection mediated by a toxin in a subject comprising administering to the subject in need of such treatment an amount sufficient to treat the infection of a composition comprising a compound of claim 1.

10. The method of claim 9 wherein the compound includes the oligosaccharide sequence α

Gal(1→

4)β

Gal.

11. The method of claim 9 wherein the compound includes the oligosaccharide sequence α

Gal(1→

4)β

Gal(1→

4)β

GlcNAc.

12. The method of claim 9 wherein the compound includes the oligosaccharide sequence α

Gal(1→

4)β

Gal(1→

4)β

Glc.

13. The method of claim 9 wherein the linker arm comprises from 6 to 10 carbon atoms.

14. The method of claim 9 wherein the linker arm is —

(CH₂)₈C(O)—

.

15. The method of claim 9 wherein the compound is covalently bound to or adsorbed onto a solid inert affinity support.

16. The method of claim 9 wherein the pharmaceutical composition is administered to the patient prior to organ involvement other than intestinal involvement.

17. The method of claim 9 wherein the compound is administered orally.

18. The method of claim 9 wherein the compound is administered via injection.

19. The method of claim 9 wherein the toxin is a pentameric toxin.

20. The method of claim 9 wherein the toxin is selected from the group consisting of SLTs, verotoxins, cholera toxin, clostridium difficile toxins A and B, bacterial pili from enteropathogenic E. coli (EPEC) and enterotoxigenic E. coli (ETEC).

21. The method of claim 20 wherein the SLTs are present in salmonella or camylobacter bacteria.

22. The method of claim 9 wherein the toxin is selected from the group consisting of viral lectins.

23. A method for diagnosing bacterial infections mediated by toxins in a patient comprising obtaining a biological sample from the patient and assaying for the presence of the toxin in a binding assay which uses a compound according to claim 1 to bind to the toxin.

24. The method of claim 23 wherein the compound includes a label selected from the group consisting of radiolabels, fluorescent tags, biotin, streptavidin, and enzymes which enable the compound to be detected after it has been bound to the toxin.