Grant: Project Grant
University of Alberta
$623,475.00
LILRB1 Genetic Variation and the Response to Human Cytomegalovirus
FY 2018-19
Summary
Cytomegalovirus is a member of the herpes virus family that causes serious complications in transplant patients and newborns, and cytomegalovirus is associated with cancer and cardiovascular disease. We are studying a cell surface protein involved in the normal regulation of the immune response that cytomegalovirus exploits to escape the immune response. There is considerable genetic variation in the receptor, which is known as LILRB1, and the variation in the viral immune evasion protein known as UL18. We previously discovered that transplant patients with distinct variants of LILRB1 do not control cytomegalovirus as well as the general population. The goal of the proposed research project is to understand why the rare individuals with the LILRB1 variants do poorly with a view to tailoring current antiviral therapies (personalized medicine) for those at highest risk post-transplant and for informing the development of a vaccine to prevent congenital infection.
Department
Program
Project Grant
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
387761
Name
Burshtyn Deborah N
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
LILRB1 Genetic Variation and the Response to Human Cytomegalovirus
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$623,475
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Gene Regulation; Immunogenetics; Inhibitory Receptors; Receptor Biology; Viral Immune Evasion
Abstract
Cytomegalovirus is a member of the herpes virus family that causes serious complications in transplant patients and newborns, and cytomegalovirus is associated with cancer and cardiovascular disease. We are studying a cell surface protein involved in the normal regulation of the immune response that cytomegalovirus exploits to escape the immune response. There is considerable genetic variation in the receptor, which is known as LILRB1, and the variation in the viral immune evasion protein known as UL18. We previously discovered that transplant patients with distinct variants of LILRB1 do not control cytomegalovirus as well as the general population. The goal of the proposed research project is to understand why the rare individuals with the LILRB1 variants do poorly with a view to tailoring current antiviral therapies (personalized medicine) for those at highest risk post-transplant and for informing the development of a vaccine to prevent congenital infection.
Competitiondate
201809
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Burshtyn, Deborah N; Cervera, Carlos; Humar, Atul
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $623,475~ $0~