US Army Medical Research and Materiel Command

Slides:



Advertisements
Similar presentations
“REACH-THROUGH CLAIMS”
Advertisements

Immuno- pathogenesis of Ebola virus disease
Monoclonal Antibodies Large scale production and their implications in AIDS research.
Lec 16 Medical biotechnology Shah Rukh Abbas, PhD
Dr Hannah Kibuuka Makerere University Walter Reed Project Presentation at the Uganda Medical Association-Uganda Veterinary Association joint conference.
Phagocyte. B cells Receptor B Cell Naïve B cell B cells and antibodies daughter cells produce antibodies phagocyte consumes an antibody coated virus.
Viruses Chapter 19. A Borrowed Life Virus: an infections particle incapable of replicating outside of a cell, which consists of an RNA or DNA genome enclosed.
After a virus becomes active and replicates in a host cell, it destroys the host cell. Copies of the virus are then released into the host organism, where.
The tale of an enveloped virus.
Technology Available for Licensing US Army Medical Research and Materiel Command A Pharmaceutical Composition Containing pGLU- GLU-PRO-NH 2 and Methods.
Rationale Marburg Hemorrhagic Fever is a highly fatal disease and it is less known than Ebola. Together, Ebola and Marburg make up the Filoviridae family.
Technology Available for Licensing US Army Medical Research and Materiel Command Recombinant Vaccine Against Botulinum Neurotoxin This invention provides.
ACTIVE AND PASSIVE IMMUNIZATION. Two types of immunization Active immunization - natural infection - vaccination, that provides people with an immunological.
Smallpox vaccine in combination with ST-246 Robert Jordan, Ph.D. SIGA Technologies, Inc FDA – Public HearingMay 17, 2007.
Examination Practice in Applications Presenting “Reach-Through Claims” George Elliott Practice Specialist Technology Center 1600
CATEGORY: VACCINES & THERAPEUTICS HIV-1 Vaccines Shokouh Makvandi-Nejad, University of Oxford, UK HIV-1 Vaccines © The copyright for this work resides.
Unit Question: What is life and how does it maintain balance? Notes #8: The Immune System and Homeostasis Aim: What does your immune system do? Name:________________.
MONOCLONAL ANTIBODIES What are they? How are they produced? What potential uses?
“Science Improving Health”
Basics of HIV Virus Vijay Kandula, MD MPH AAHIVS
Antiviral Medications
Good teaching is more a giving of right questions than a giving of right answers. – Josef Albers Viruses Chapter 19.
HIV-1 Vaccines Shokouh Makvandi-Nejad, University of Oxford, UK
Question of the day Q: What relationship do some bacteria have with their host organisms? A: Q: Name a situation where bacteria is “helpful”.
Viral pathogens and Vaccination
“Science Improving Health”
Globular Protein Made of amino acid chains
Characteristics of Viruses
In Vivo Production of Monoclonal Antibodies by Gene Transfer via Electroporation Protects against Lethal Influenza and Ebola Infections  Chasity D. Andrews,
AIDS supplement.
US Army Medical Research and Materiel Command
“Science Improving Health”
by Peter Ruf, and Horst Lindhofer
US Army Medical Research and Materiel Command
A typical enveloped virus
US Army Medical Research and Materiel Command
“Science Improving Health”
US Army Medical Research and Materiel Command
Page 21 EQ: How do Viruses compare to cells? How do viruses replicate?
Volume 10, Issue 4, Pages (April 1999)
M. Juliana McElrath, Barton F. Haynes  Immunity 
New Hope in the Search for Ebola Virus Treatments
Viruses.
US Army Medical Research and Materiel Command
US Army Medical Research and Materiel Command
In vivo prophylactic and therapeutic efficacy of C12G6 in mice
Viruses Viruses – are segments of nucleic acids
by Guntur Fibriansah, Kristie D. Ibarra, Thiam-Seng Ng, Scott A
Obiltoxaximab Drugbank ID :DB05336 Molecular Weight (Daltons) :148000
Volume 6, Issue 4, Pages (October 2009)
Viral Diseases How do vaccines work?.
Humoral and Cell Mediated Immunity
US Army Medical Research and Materiel Command
US Army Medical Research and Materiel Command
In Vivo Production of Monoclonal Antibodies by Gene Transfer via Electroporation Protects against Lethal Influenza and Ebola Infections  Chasity D. Andrews,
Virus Characteristics
Development of Effective Vaccines against Pandemic Influenza
US Army Medical Research and Materiel Command
Good teaching is more a giving of right questions than a giving of right answers. – Josef Albers Viruses Chapter 19.
US Army Medical Research and Materiel Command
Viruses TEK 4C: Compare structures of viruses to cells, describe viral reproduction, and describe the role of viruses in causing diseases such as HIV and.
US Army Medical Research and Materiel Command
US Army Medical Research and Materiel Command
US Army Medical Research and Materiel Command
US Army Medical Research and Materiel Command
Strategies of CMV envelope protein-mediated immune evasion.
US Army Medical Research and Materiel Command
In vivo prophylactic and therapeutic efficacy of C12G6 in mice
PDL192 and inhibit the growth of xenograft tumors.
Viruses Viruses – are segments of nucleic acids
Presentation transcript:

US Army Medical Research and Materiel Command Technology Available for Licensing Monoclonal Antibodies to Ebola Glycoprotein This invention provides a method for using individual antibodies or mixtures thereof for the detection, prevention, and therapeutic treatment of Ebola virus infections, both in vitro and in vivo. The invention describes Ebola glycoprotein (GP) monoclonal antibodies (Mabs) and epitopes recognized by these Mabs. The invention includes several different Mabs against Ebola viral strains that are representative of five different antibody types. The MAbs were protective against Ebola challenge when administered prophylactically or therapeutically to mice. Ebola viruses cause acute, lethal hemorrhagic fevers in humans and nonhuman primates. No vaccines or treatments currently exist against these viruses. Understanding of the immune mechanisms that mediate protection is limited. The membrane-anchored viral GP is the only one known to occur on the surfaces of both virions and infected cells, and is presumed responsible for receptor binding and fusion of the virus with host cells. Ebola GP may therefore be an important target of protective antibodies. For the most effective Mabs, the amount required to protect mice was within an achievable human therapeutic dose of 3 – 5 mg/kg. Some of the Mabs were effective when administered two days after challenge, during which significant viral replication had occurred. Features and advantages: • Protects BALB/C strain mice from a lethal challenge with mouse-adapted Ebola Zaire virus • Protects C57BL/6 strain mice from a similar challenge • Binds specifically to epitopes on the Ebola virus GP • Mabs are of the IgG1 and IgG2a subclass • Can produce Mabs with desired characteristics by phage display, or common cell line types • Can prepare as a mixture of Mabs to prevent, treat, and detect infections Patent Status Patent No.: 6,630,144 Available from: www.uspto.gov Issued: October 7, 2003 Docket No.: RIID 99-28 Point of Contact Dr. Paul C. Mele Director, Office of Research and Technology Applications USAMRMC, MCMR-ZA-J 504 Scott St., Ft. Detrick, MD 21702-5012 E-mail: paul.mele@amedd.army.mil Voice: 301-619-6664/2032/7219 Fax: 301-619-5034 KEYWORDS: Ebola; monoclonal antibodies; protection; production; animal studies Licensing Opportunities • Patent licenses are available to companies with commercial interests