Modified antibodies for enhanced hepatocyte clearance

Claim 2

In a method of treating a human patient having a tumor or infectious lesion, comprising parenterally, but non-systemically, injecting into said patient a therapeutically effective amount of an antibody or antibody fragment, conjugated to a radioisotope, toxin or drug, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 3

The method of claim 1, wherein said conjugated glycoside residue is a galactose, N-acetylgalactosamine or glucose residue.

Claim 4

The method of claim 1, wherein said antibody or antibody fragment is conjugated to a radioisotope.

Claim 5

The method of claim 1, wherein said antibody or antibody fragment is conjugated to a drug or toxin.

Claim 6

The method of claim 1, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with a tumor.

Claim 7

The method of claim 5, wherein said tumor is an ovarian tumor.

Claim 8

The method of claim 1, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with an infectious lesion.

Claim 9

The method of claim 1, wherein said non-systemic parenteral injection is effected by an intraperitoneal route.

Claim 10

The method of claim 1, which further comprises reducing the rate of efflux of said conjugate into the bloodstream.

Claim 11

In a method of treating a human patient having a tumor or infectious lesion, comprising parenterally, but non-systemically, injecting into said patient a therapeutically effective amount of an antibody or antibody fragment which specifically binds to a marker produced by or associated with said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment is modified by being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 12

In a method of treating a human patient having a tumor or infectious lesion, comprising parenterally, but non-systemically, injecting into said patient a therapeutically effective amount of an antibody or antibody fragment which specifically binds to a marker produced by or associated with said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment is modified by being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 13

The method of claim 10, wherein said conjugated glycoside residue is a galactose, N-acetylgalactosamine or glucose residue.

Claim 14

The method of claim 10, wherein said antibody or antibody fragment specifically binds to a marker produced by or associated with a tumor.

Claim 15

The method of claim 12, wherein said tumor is an ovarian tumor.

Claim 16

In a method of treating a human patient having a tumor or infectious lesion, comprising injecting into said patient intravenously a therapeutically effective amount of an antibody or antibody fragment, conjugated to a radioisotope, toxin or drug, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion, The improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and wherein said method further comprises injecting into said patient intravenously, at, prior to or subsequent to the injection of said modified antibody or antibody fragment conjugate, an amount of a competitive inhibitor of binding to the hepatocyte asialoglycoprotein receptor sufficient to inhibit or significantly retard hepatocyte clearance of circulating modified conjugate, for a time sufficient to permit uptake of said modified conjugate by said tumor or infectious lesion, after which time said modified conjugate is cleared from the circulation.

Claim 17

In a method of treating a human patient having a tumor or infectious lesion, comprising injecting into said patient intravenously a therapeutically effective amount of an antibody or antibody fragment, conjugated to a radioisotope, toxin or drug, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion, The improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and wherein said method further comprises injecting into said patient intravenously, at, prior to or subsequent to the injection of said modified antibody or antibody fragment conjugate, an amount of a competitive inhibitor of binding to the hepatocyte asialoglycoprotein receptor sufficient to inhibit or significantly retard hepatocyte clearance of circulating modified conjugate, for a time sufficient to permit uptake of said modified conjugate by said tumor or infectious lesion, after which time said modified conjugate is cleared from the circulation.

Claim 18

In a method of imaging a human patient having a tumor or infectious lesion, comprising parenterally, but non-systemically, injecting into said patient a diagnostically effective amount of an antibody or antibody fragment, conjugated to a radioisotope or magnetic resonance image enhancing agent, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion; and obtaining a scintigraphic or magnetic resonance image of said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 19

In a method of imaging a human patient having a tumor or infectious lesion, comprising parenterally, but non-systemically, injecting into said patient a diagnostically effective amount of an antibody or antibody fragment, conjugated to a radioisotope or magnetic resonance image enhancing agent, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion; and obtaining a scintigraphic or magnetic resonance image of said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 20

The method of claim 15, wherein said conjugated glycoside residue is a galactose, N-acetylgalactosamine or glucose residue.

Claim 21

The method of claim 15, wherein said antibody or antibody fragment is conjugated to a radioisotope, and a scintigraphic image is obtained.

Claim 22

The method of claim 15, wherein said antibody or antibody fragment is conjugated to a magnetic resonance image enhancing agent, and a magnetic resonance image is obtained.

Claim 23

The method of claim 15, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with a tumor.

Claim 24

The method of claim 19, wherein said tumor is an ovarian tumor.

Claim 25

In a method of imaging a human patient having a tumor or infectious lesion, comprising injecting into said patient intravenously a diagnostically effective amount of an antibody or antibody fragment, conjugated to a radioisotope or magnetic resonance image enhancing agent, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion; and obtaining a scintigraphic or magnetic resonance image of said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminated glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and wherein said method further comprises injecting into said patient intravenously, at, prior to or subsequent to the injection of said modified antibody or antibody fragment conjugate, an amount of a competitive inhibitor of binding to the hepatocyte asialoglycoprotein receptor sufficient to inhibit or significantly retard hepatocyte clearance of circulating modified conjugate, for a time sufficient to permit uptake of said modified conjugate by said tumor or infectious lesion, after which time said modified conjugate is cleared from the circulation.

Claim 26

In a method of imaging a human patient having a tumor or infectious lesion, comprising injecting into said patient intravenously a diagnostically effective amount of an antibody or antibody fragment, conjugated to a radioisotope or magnetic resonance image enhancing agent, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with said tumor or infectious lesion; and obtaining a scintigraphic or magnetic resonance image of said tumor or infectious lesion, the improvement wherein said antibody or antibody fragment conjugate is modified by being further conjugated to, or having exposed thereon, a plurality of terminated glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and wherein said method further comprises injecting into said patient intravenously, at, prior to or subsequent to the injection of said modified antibody or antibody fragment conjugate, an amount of a competitive inhibitor of binding to the hepatocyte asialoglycoprotein receptor sufficient to inhibit or significantly retard hepatocyte clearance of circulating modified conjugate, for a time sufficient to permit uptake of said modified conjugate by said tumor or infectious lesion, after which time said modified conjugate is cleared from the circulation.

Claim 27

The method of claim 21, wherein said conjugated glycoside residue is a galactose, N-acetylgalactosamine or glucose residue.

Claim 28

The method of claim 21, wherein said antibody or antibody fragment is conjugated to a radioisotope, and a scintigraphic image is obtained.

Claim 29

The method of claim 21, wherein said antibody or antibody fragment is conjugated to a magnetic resonance image enhancing agent, and a magnetic resonance image is obtained.

Claim 30

The method of claim 21, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with a tumor.

Claim 31

A modified antibody conjugate, comprising an antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to a radioisotope, a magnetic resonance image enhancing agent, a toxin or a drug, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 32

A modified antibody conjugate, comprising an antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to a radioisotope, a magnetic resonance image enhancing agent, a toxin or a drug, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor.

Claim 33

The modified antibody conjugate of claim 26, wherein said conjugated glycoside residue is a galactose, N-acetylgalactosamine or glucose residue.

Claim 34

The modified antibody conjugate of claim 26, wherein said antibody or antibody fragment is conjugated to a radioisotope.

Claim 35

The modified antibody conjugate of claim 26, wherein said antibody or antibody fragment is conjugated to a magnetic resonance image enhancing agent.

Claim 36

The modified antibody conjugate of claim 26, wherein said antibody or antibody fragment specifically binds to a marker produced by or associated with a tumor.

Claim 37

The modified antibody conjugate of claim 30, wherein said tumor is an ovarian tumor.

Claim 38

The modified antibody conjugate of claim 26, wherein said antibody or antibody fragment conjugate specifically binds to a marker produced by or associated with an infectious lesion.

Claim 39

A sterile, injectable preparation for human therapeutic use, comprising: (a) a therapeutically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 40

A sterile, injectable preparation for human therapeutic use, comprising: (a) a therapeutically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 41

A sterile, injectable preparation for imaging a tumor or infectious lesion in a human patient, comprising: (a) a diagnostically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to a radioisotope or a magnetic resonance image enhancing agent, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 42

A sterile, injectable preparation for imaging a tumor or infectious lesion in a human patient, comprising: (a) a diagnostically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to a radioisotope or a magnetic resonance image enhancing agent, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 43

A kit for preparing a sterile, injectable preparation for human therapeutic use, comprising, in one or more suitable sterile containers: (a) a therapeutically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 44

A kit for preparing a sterile, injectable preparation for human therapeutic use, comprising, in one or more suitable sterile containers: (a) a therapeutically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 45

The kit of claim 35, which further comprises (c) an effective inhibiting amount of a competitive inhibitor of binding to the human hepatocyte asialoglycoprotein receptor.

Claim 46

A kit for preparing a sterile, injectable preparation for imaging a tumor or infectious lesion in a human patient, comprising, in one or more suitable sterile containers: (a) a diagnostically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to or adapted for conjugation to a radioisotope or magnetic resonance image enhancing agent, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 47

A kit for preparing a sterile, injectable preparation for imaging a tumor or infectious lesion in a human patient, comprising, in one or more suitable sterile containers: (a) a diagnostically effective amount of a modified antibody or antibody fragment which specifically binds a marker which is produced by or associated with a tumor or infectious lesion, said antibody or antibody fragment being conjugated to or adapted for conjugation to a radioisotope or magnetic resonance image enhancing agent, said antibody or antibody fragment being further conjugated to, or having exposed thereon, a plurality of terminal glycoside residues which bind to the human hepatocyte asialoglycoprotein receptor; and (b) a pharmaceutically acceptable sterile injection vehicle.

Claim 48

The kit of claim 37, which further comprises (c) an effective inhibiting amount of a competitive inhibitor of binding to the human hepatocyte asialoglycoprotein receptor.

Claim 49

The method of claim 1, wherein said glycoside residue is a galactose residue.

Claim 50

The method of claim 10, wherein said glycoside residue is a galactose residue.

Claim 51

The method of claim 15, wherein said glycoside residue is a galactose residue.

Claim 52

The method of claim 21, wherein said glycoside residue is a galactose residue.

Claim 53

The modified antibody conjugate of claim 26, wherein said glycoside residue is a galactose residue.