IP Library Granted Patent US 7,858,298
Granted Patent B1
US 7,858,298 · App. 09/460,216 · Granted Dec 28, 2010

Methods of inhibiting human immunodeficiency virus type 1 (HIV-1) infection through the administration of CCR5 chemokine receptor antagonists

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,858,298
App. No.
09/460,216
Granted
Dec 28, 2010
Kind
B1
Abstract

This invention provides methods for inhibiting fusion of HIV-1 to CD4 + cells which comprise contacting CD4 + cells with a non-chemokine agent capable of binding to a chemokine receptor in an amount and under conditions such that fusion of HIV-1 to the CD4 + cells is inhibited. This invention also provides methods for inhibiting HIV-1 infection of CD4 + cells which comprise contacting CD4 + cells with a non-chemokine agent capable of binding to a chemokine receptor in an amount and under conditions such that fusion of HIV-1 to the CD4 + cells is inhibited, thereby inhibiting the HIV-1 infection. This invention provides non-chemokine agents capable of binding to the chemokine receptor and inhibiting fusion of HIV-1 to CD4 + cells. This invention also provides pharmaceutical compositions comprising an amount of the non-chemokine agent capable of binding to the chemokine receptor and inhibiting fusion of HIV-1 to CD4 + cells effective to prevent fusion of HIV-1 to CD4 + cells and a pharmaceutically acceptable carrier.

Claims (13)

1. A method of inhibiting fusion of a CCR5+, CD4+ human cell by with a macrophage-tropic HIV-1, which comprises contacting the CCR5+, CD4+ cell with a non-chemokine agent which is a CCR5 chemokine receptor antagonist which

(a) binds to the CCR5 chemokine receptor on the surface of the CCR5+, CD4+ cell;

(b) competes with RANTES, MIP-1α and MIP-1β for binding to the CCR5 chemokine receptor on the surface of the CCR5+, CD4+ cell;

(c) inhibits binding of HIV1 JR-FL gp120 to the CCR5+, CD4+ cell;

(d) inhibits fusion of HIV-1 JR-FL with a PM-1 cell;

(e) does not inhibit fusion of HIV-1 BRU with a PM-1 cell; and

(f) does not activate an inflammatory response upon binding to the CCR5 chemokine receptor on the surface of the CCR5+, CD4+ cell;

in an amount and under conditions such that fusion of the macrophage-tropic HIV-1 with the CCR5+, CD4+ cell is inhibited.

2. The method of claim 1 , wherein the CCR5 chemokine receptor antagonist is a polypeptide.

3. The method of claim 1 , wherein the CCR5 chemokine receptor antagonist is a non-chemokine peptide obtained by adding amino acids to, or deleting amino acids from, the N-terminus of a chemokine selected from the group consisting of RANTES, MIP-1α and MIP-1β.

4. The method of claim 1 , wherein the CCR5 chemokine receptor antagonist is an antibody or a portion of an antibody.

5. The method of claim 4 , wherein the CCR5 chemokine receptor antagonist is a monoclonal antibody or a portion of a monoclonal antibody.

6. The method of claim 4 , wherein the CCR5 chemokine receptor antagonist is a polyclonal antibody.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2013
From: PROGENICS PHARMACEUTICALS, INC.
To: CYTODYN, INC.
Reel/Frame 029633/0837 →