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Monthly Featured Technologies |
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CC Chemokine Receptor 5 DNA, New Animal Models and Therapeutic Agents for HIV Infection
Description of Technology:
Chemokine receptors are expressed by many cells, including lymphoid cells, and function to mediate cell trafficking and localization. CC chemokine receptor 5 (CCR5) is a seven-transmembrane, G protein-coupled receptor (GPCR) which regulates trafficking and effector functions of memory/effector T-lymphocytes, macrophages, and immature dendritic cells. Chemokine binding to CCR5 leads to cellular activation through pertussis toxin-sensitive heterotrimeric G proteins as well as G protein-independent signalling pathways. Like many other GPCRs, CCR5 is regulated by agonist-dependent processes which involve G protein coupled receptor kinase (GRK)-dependent phosphorylation, beta-arrestin-mediated desensitization and internalization.
Human CCR5 also functions as the main coreceptor for the fusion and entry of many strains of human immunodeficiency virus (HIV-1, HIV-2). HIV-1 transmission almost invariably involves such CCR5-specific variants (designated R5); individuals lacking functional CCR5 (by virtue of homozygosity for a defective CCR5 allele) are almost completely resistant to HIV-1 infection. Specific blocking of CCR5 (e.g. with chemokine ligands, anti-CCR5 antibodies, CCR5-blocking low MW inhibitors, etc.) inhibits entry/infection of target cells by R5 HIV strains. Cells expressing CCR5 and CD4 are useful for screening for agents that inhibit HIV by binding to CCR5. Such agents represent potential new approaches to block HIV transmission and to treat infected people. A small animal expressing both human CCR5 along with human CD4 supports entry of HIV into target cells, a necessary hurdle that must be overcome for development of a small animal model (e.g. transgenic mouse, rat, rabbit, mink) to study HIV infection and its inhibition.
The invention embodies the CCR5 genetic sequence, cell lines and transgenic animals, the cells of which coexpress human CD4 and CCR5, and which may represent valuable tools for the study of HIV infection and for screening anti-HIV agents. The invention also embodies anti-CCR5 agents that block HIV env-mediated membrane fusion associated with HIV entry into human CD4-positive target cells or between HIV-infected cells and uninfected human CD4-positive target cells.
Inventors:
Christophe Combadiere (NIAID), Yu Feng (NIAID), Ghalib Alkahatib (NIAID), Edward A. Berger (NIAID), Philip M. Murphy (NIAID), Christopher C. Broder (NIAID), Paul E. Kennedy (NIAID)
Publication:
G Alkhatib et al. CC CKR5: a RANTES, MIP-1alpha, MIP-1beta receptor as a fusion cofactor for macrophage-tropic HIV-1. Science. 1996 Jun 28;272(5270):1955-1958. [PubMed abs]
Patent Status:
DHHS Reference No. E-090-1996/0 --
U.S. Provisional Application No. 60/018,508 filed 28 May 1996
U.S. Patent Application No. 08/864,458 filed 28 May 1997
U.S. Patent Application No. 10/439,845 filed 15 May 2003
U.S. Patent No. 7,151,087 issued 19 Dec 2006
U.S. Patent Application No. 10/846,185 filed 14 May 2004
U.S. Patent No. 7,374,872 issued 20 May 2008
U.S. Patent Application No. 12/044,845 filed 07 Mar 2008
PCT Application No. PCT/US97/09586 filed 28 May 1997
European Patent Application No. 97929777.7 filed 28 May 1997
Licensing Status:
This technology is available for exclusive or nonexclusive licensing.
Collaborative Research Opportunity:
The NIAID Laboratory of Molecular Immunology and Laboratory of Viral Diseases are seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize CCR5-related products. Please contact Philip Murphy (301-496-8616, pmm@nih.gov) or Edward Berger (301-402-2481, edward_berger@nih.gov) for more information.
Portfolios:
Infectious Diseases - Therapeutics, anti-virals, AIDS
Infectious Diseases - Research Materials
For additional information, please contact:
Peter A. Soukas, J.D.
Office of Technology Transfer
National Institutes of Health
6011 Executive Boulevard, Suite 325
Rockville MD 20852
Phone: 301/435-4646
Fax: 301/402-0220
Email: soukasp@mail.nih.gov
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