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Grant: Operating Grant: Industry-partnered Collaborative Research

University of British Columbia

$576,493.00

Discovery & Development of Novel Small Molecule Inhibitors of Viroporin Proteins for the Treatment of Acute & Chronic Viral Infections.

FY 2011-12

Summary
The public enjoys protection from viral infectious diseases through the use of modern day vaccines. However, when vaccines are not possible, medications are available to reduce the effects of certain viruses such as herpes simplex, influenza, shingles, cytomegalovirus, and even HIV-1, the cause of acquired immune deficiency syndrome (AIDS). Notably, very new medications for hepatitis C (HCV), for which there is no vaccine, show particular promise by targeting key steps in the HCV life cycle. However, the need for newer, more effective antiviral medications remains a priority as new viruses invade naïve populations and conditions in developing countries continue to allow for the propagation of neglected viral diseases. For example, Dengue, Chikungunya, West Nile, new strains of HCV, and pandemic influenza variants are emerging threats. Many of these emerging viruses have also been resistant to vaccine development, further underscoring the need to develop new medications. This proposal is designed to exploit new antiviral targets called viroporins, which appear to be involved in virus life cycles. Initially studied for influenza, the viroporins have now been characterized in many viruses, and recent data suggest that viroporins may be a viable therapeutic intervention for many viral infectious diseases. In this proposal, we will 1) Develop the means to identify molecules that can inhibit the viroporins of several problem viruses; 2) Determine the effectiveness of identified molecules to block the life cycles of HCV, Dengue, and Influenza viruses.
Program
Operating Grant: Industry-partnered Collaborative Research
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
255430
Name
Fedida David
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Cardiome Pharma Corp. (Vancouver, B.C,)
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Industry Partnered Collaborative Research
Projecttitle
Discovery & Development of Novel Small Molecule Inhibitors of Viroporin Proteins for the Treatment of Acute & Chronic Viral Infections.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$576,493
Cihrequipment2
$0
Programname2
Operating Grant: Industry-partnered Collaborative Research
Keyworddelim
Dengue Fever; Hepatitis C; Influenza M2; Ion Channels; Viroporins
Abstract
The public enjoys protection from viral infectious diseases through the use of modern day vaccines. However, when vaccines are not possible, medications are available to reduce the effects of certain viruses such as herpes simplex, influenza, shingles, cytomegalovirus, and even HIV-1, the cause of acquired immune deficiency syndrome (AIDS). Notably, very new medications for hepatitis C (HCV), for which there is no vaccine, show particular promise by targeting key steps in the HCV life cycle. However, the need for newer, more effective antiviral medications remains a priority as new viruses invade naïve populations and conditions in developing countries continue to allow for the propagation of neglected viral diseases. For example, Dengue, Chikungunya, West Nile, new strains of HCV, and pandemic influenza variants are emerging threats. Many of these emerging viruses have also been resistant to vaccine development, further underscoring the need to develop new medications. This proposal is designed to exploit new antiviral targets called viroporins, which appear to be involved in virus life cycles. Initially studied for influenza, the viroporins have now been characterized in many viruses, and recent data suggest that viroporins may be a viable therapeutic intervention for many viral infectious diseases. In this proposal, we will 1) Develop the means to identify molecules that can inhibit the viroporins of several problem viruses; 2) Determine the effectiveness of identified molecules to block the life cycles of HCV, Dengue, and Influenza viruses.
Competitiondate
201203
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Fedida, David
Approvedterm
3 ans 0 mois
Cihrcontribution2
Knowledge Translation Branch~ $576,493~ $0~
University of British Columbia - $576,493 Grant (2011… | Canada Spends