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Grant: Project Grant

McGill University

$905,935.00

The impact of perturbations in T cell migration on the spatio-temporal dynamics of CD4 T cell homeostasis and effector cell differentiation

FY 2015-16

Summary
In our global society, many of us travel to and from work, fly between cities, or even set up residence somewhere new. Along the way, we might bump into others, exchange information, and learn new things that inform our behaviour. Hence, what we learn during our travels can have a dramatic impact on our lives. T lymphocytes have a similarly cosmopolitan lifestyle within the body. The job of T cells in the immune system - to detect and stop the replication of a pathogen or cancer cell as quickly as possible - makes it essential for them to commute continuously between the blood and secondary lymphoid organs. Within lymphoid organs, T cells make critical interactions with other cells that dictate their function and fate. During infections, such interactions can license them to enter tissues and even set up residence there, protecting from reinfection. To understand the implications of the jet-setting behaviour of T cells on their function, we use advanced microscopy to track their movements within tissues in real time. This approach enables us to investigate a number of important questions. How do the interactions T cells make with other cells keep them alive? Why do pathogens or gene defects that prevent migration lead paradoxically both to severe immune deficiencies and to immune-mediated disease? In the long-term, answers to these questions will contribute to the design of better therapies for immunological diseases, such as allergy and autoimmunity, and allow us to harness the function of T cells to improve our ability to treat or prevent infections, from Ebola virus to HIV and beyond.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
343890
Name
Mandl Judith N
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
The impact of perturbations in T cell migration on the spatio-temporal dynamics of CD4 T cell homeostasis and effector cell differentiation
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$905,935
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
2-Photon Microscopy; Cd4 T Cells; Cell Migration; Cellular Interaction Dynamics; Dendritic Cells; Dock8; Effector Cell Differentiation; Homeostasis; Mouse Models; Primary Immunodeficiency
Abstract
In our global society, many of us travel to and from work, fly between cities, or even set up residence somewhere new. Along the way, we might bump into others, exchange information, and learn new things that inform our behaviour. Hence, what we learn during our travels can have a dramatic impact on our lives. T lymphocytes have a similarly cosmopolitan lifestyle within the body. The job of T cells in the immune system - to detect and stop the replication of a pathogen or cancer cell as quickly as possible - makes it essential for them to commute continuously between the blood and secondary lymphoid organs. Within lymphoid organs, T cells make critical interactions with other cells that dictate their function and fate. During infections, such interactions can license them to enter tissues and even set up residence there, protecting from reinfection. To understand the implications of the jet-setting behaviour of T cells on their function, we use advanced microscopy to track their movements within tissues in real time. This approach enables us to investigate a number of important questions. How do the interactions T cells make with other cells keep them alive? Why do pathogens or gene defects that prevent migration lead paradoxically both to severe immune deficiencies and to immune-mediated disease? In the long-term, answers to these questions will contribute to the design of better therapies for immunological diseases, such as allergy and autoimmunity, and allow us to harness the function of T cells to improve our ability to treat or prevent infections, from Ebola virus to HIV and beyond.
Competitiondate
201603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Mandl, Judith N
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $905,935~ $0~
McGill University - $905,935 Grant (2015-16) | Canada Spends