Christophe Combadiere - Paris, FR Yu Feng - San Diego CA, US Ghalib Alkhatib - Carmel IN, US Edward A. Berger - Rockville MD, US Philip M. Murphy - Rockville MD, US Christopher C. Broder - Rockville MD, US Paul E. Kennedy - Silver Spring MD, US
Assignee:
The United States of America as represented by the Department of Health and Human Resources - Washington DC
International Classification:
A61K 38/00
US Classification:
514 13, 514 14
Abstract:
The susceptibility of human macrophages to human immunodeficiency virus (HIV) infection depends on cell surface expression of the human CD4 molecule and CC cytokine receptor 5. CCR5 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CCR5 plays an essential role in the membrane fusion step of infection by some HIV isolates. The establishment of stable, nonhuman cell lines and transgenic mammals having cells that coexpress human CD4 and CCR5 provides valuable tools for the continuing research of HIV infection. In addition, antibodies which bind to CCR5, CCR5 variants, and CCR5-binding agents, capable of blocking membrane fusion between HIV and target cells represent potential anti-HIV therapeutics for macrophage-tropic strains of HIV.
Compositions And Methods For Production Of Rna Viruses And Rna Virus-Based Vector Particles
The invention provides methods to produce RNA viral sequences, recombinant RNA viruses, mutants of RNA viruses and RNA virus-derived vectors in cell culture and in vitro using non-viable, replication defective, helper vaccinia recombinants. These methods allow generation of RNA virus sequences and viral particles in cell culture and in vitro independent of their natural replication pathways, bypassing the limitation of any cellular barriers. The invention also provides novel RNA viral sequences and viral particles using these methods.
Cc Chemokine Receptor 5 Dna, New Animal Models And Therapeutic Agents For Hiv Infection
Christophe Combadiere - Rockville MD, US Yu Feng - San Diego CA, US Ghalib Alkhatib - Bethesda MD, US Edward Berger - Rockville MD, US Philip Murphy - Rockville MD, US Christopher Broder - Rockville MD, US Paul Kennedy - Silver Spring MD, US
The susceptibility of human macrophages to human immunodeficiency virus (HIV) infection depends on cell surface expression of the human CD4 molecule and CC cytokine receptor 5. CCR5 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CCR5 plays an essential role in the membrane fusion step of infection by some HIV isolates. The establishment of stable, nonhuman cell lines and transgenic mammals having cells that coexpress human CD4 and CCR5 provides valuable tools for the continuing research of HIV infection. In addition, antibodies which bind to CCR5, CCR5 variants, and CCR5-binding agents, capable of blocking membrane fusion between HIV and target cells represent potential anti-HIV therapeutics for macrophage-tropic strains of HIV.
Cells Expressing Both Human Cd4 And A Human Fusion Accessory Factor Associated With Hiv Infection
The susceptibility to human immunodeficiency virus (HIV) infection depends on the cell surface expression of the human CD4 molecule and a human fusion accessory factor associated with HIV infection (CXCR4). CXCR4 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CXCR4 plays an essential role in the membrane fusion step of HIV infection. The establishment of stable, nonhuman cell lines and transgenic mammals having cells that coexpress human CD4 and CXCR4 provides valuable tools for the continuing research of HIV infection and the development of more effective anti-HIV therapeutics. In addition, antibodies against CXCR4, isolated and purified peptide fragments of CXCR4, and CXCR4-binding biologic agents, capable of blocking membrane fusion between HIV and target cells represent potential anti-HIV therapeutics.
Cc Chemokine Receptor 5 Dna, New Animal Models And Therapeutic Agents For Hiv Infection
Christophe Combadiere - Paris, FR Yu Feng - San Diego CA, US Ghalib Alkhatib - Carmel IN, US Edward Berger - Rockville MD, US Philip Murphy - Rockville MD, US Christopher Broder - Rockville MD, US Paul Kennedy - Silver Spring MD, US
International Classification:
A61K 31/70 C12P 21/06 A01N 43/04
US Classification:
514044000, 435069100
Abstract:
The susceptibility of human macrophages to human immunodeficiency virus (HIV) infection depends on cell surface expression of the human CD4 molecule and CC cytokine receptor 5. CCR5 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CCR5 plays an essential role in the membrane fusion step of infection by some HIV isolates. The establishment of stable, nonhuman cell lines and transgenic mammals having cells that coexpress human CD4 and CCR5 provides valuable tools for the continuing research of HIV infection. In addition, antibodies which bind to CCR5, CCR5 variants, and CCR5-binding agents, capable of blocking membrane fusion between HIV and target cells represent potential anti-HIV therapeutics for macrophage-tropic strains of HIV.
Cc Chemokine Receptor 5 Dna, New Animal Models And Therapeutic Agents For Hiv Infection
Christophe Combadiere - Paris, FR Yu Feng - San Diego CA, US Ghalib Alkhatib - Carmel IN, US Edward A. Berger - Rockville MD, US Philip M. Murphy - Rockville MD, US Christopher C. Broder - Rockville MD, US Paul E. Kennedy - Silver Spring MD, US
The susceptibility of human macrophages to human immunodeficiency virus (HIV) infection depends on cell surface expression of the human CD4 molecule and CC cytokine receptor 5. CCR5 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CCR5 plays an essential role in the membrane fusion step of infection by some HIV isolates. The establishment of stable, nonhuman cell lines and transgenic mammals having cells that coexpress human CD4 and CCR5 provides valuable tools for the continuing research of HIV infection. In addition, antibodies which bind to CCR5, CCR5 variants, and CCR5-binding agents, capable of blocking membrane fusion between HIV and target cells represent potential anti-HIV therapeutics for macrophage-tropic strains of HIV.
Cells Expressing Both Human Cd4 And A Human Fusion Accessory Factor Associated With Hiv Infection
Edward Berger - Rockville MD Yu Feng - San Diego CA Paul Kennedy - Silver Spring MD Christopher Broder - Rockville MD
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC
International Classification:
C12N 1500 C12N 1563 C12N 1509 C12N 500
US Classification:
435325
Abstract:
The susceptibility to human immunodeficiency virus (HIV) infection depends on the cell surface expression of the human CD4 molecule and a human fusion accessory factor associated with HIV infection (CXCR4). CXCR4 is a member of the 7-transmembrane segment superfamily of G-protein-coupled cell surface molecules. CXCR4 plays an essential role in the membrane fusion step of HIV infection. The establishment of stable cell lines that coexpress human CD4 and CXCR4 provides valuable tools for the continuing research of HIV infection and the development of more effective anti-HIV therapeutics.
Methods And Compositions For Inhibiting Hiv Infection Of Cells By Cleaving Hiv Co-Receptor Rna
Markley C. Leavitt - La Jolla CA Richard Tritz - San Diego CA Yu Feng - San Diego CA Jack Barber - San Diego CA Mang Yu - San Diego CA
Assignee:
Immusol Incorporated - San Diego CA
International Classification:
C07H 2102
US Classification:
536 231
Abstract:
Methods of inhibiting HIV infection by blocking HIV co-receptor RNA expression are provided. Ribozymes which cleave HIV co-receptor RNA and inhibit HIV infection of cells are also provided. Co-receptor targets include fusin and CKR5.
Oct 2011 to 2000 ServerInternational Elementary School Students
Oct 2012 to Jun 2013 Private English TutorJJ Magic Kitchen Restaurant Industry, CA Aug 2009 to Mar 2011 ServerHsi-Lai Temple Hacienda Heights, CA May 2008 to Aug 2008 Volunteer
Education:
University of Pittsburgh Pittsburgh, PA May 2014 Bachelor of Art in PhilosophyNational Chengchi University Jun 2013 Philosophy
Skills:
Languages: Mandarin (Native), English (fluent). Both verbal and written. Microsoft Office: Words, Excel, Powerpoint, Outlook. U.S. C class driver's licence.
Jan 2012 to 2000 Program Manager & EngineerCharles Dunn Company, Inc Los Angeles, CA Jun 2011 to Aug 2011 Marketing and Research Analyst (Intern)Penn State University
Feb 2011 to May 2011 Graduate Student Research AssistantPenn State University
Jan 2010 to Apr 2010 Graduate Student Research AssistantDalian Zhenxin Canned Food Co., Ltd Dalian, CN Jan 2009 to Sep 2009 Production Manager and Business Coordinator (Intern)Mobile Barcode Technology
Mar 2009 to Jul 2009 Jingtang Port Logistics Systems Development
Education:
The Pennsylvania State University University Park, PA Dec 2011 Master of Engineering in Industrial EngineeringDalian University of Technology Dalian, CN Jul 2009 B.Eng. in Mechanical Engineering & B.ARoyal Institute of Technology Stockholm, ME Jan 2008 to Jul 2008 GD&T in Engineering and Management
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Project Management, Statistics, Quality Control, Engineering Economics, Operation Research &Management, Multiple Criteria Optimization, Optimization modeling, Stochastic Processes, Decision Analysis Proficient in Office (Word, Excel, PowerPoint, Project, Publisher), PLEX, Minitab, SAS, MATLAB, LINDO, Delphi Familiar with programming language SQL, C++ Speak Fluent Chinese (Mandarin) and English