Grant: Operating Grant
University of Toronto
$726,000.00
IgA Plasma Cells: Where, How and What
EF 2012-13
Résumé
B lymphocytes are an important component of the immune system due to their ability to produce antibodies, molecules that can neutralize pathogens. Such antibody responses occur when B lymphocytes that are specific for the pathogen obtain help from pathogen-specific T lymphocytes. These cellular interactions take place within a complex microenvironment called the Germinal Centre which is located within lymph nodes or the spleen. However, it takes approximately one week to initiate a Germinal Centre response, and this puts the host at risk of succumbing to infection in the early days post-exposure. As a stop-gap, humans have an innate immune system that responds rapidly to microbial exposure. Interestingly, even though B and T lymphocytes are considered part of the adaptive immune system, some B and T lymphocytes have innate properties. This is particularly true in the mucosal tissues (gut, lung, reproductive tract) and in the skin, all of which are locations where pathogens first invade our bodies. We know much less about innate lymphocytes and how they participate in immune response compared to their adaptive counterparts. We are studying innate B cell responses, with particular focus on those innate responses that occur in the gut. In particular, we are interested in how innate B cells produce the mucosal antibody IgA, and whether IgA-secreting B cells may have special properties that allow them to fight off infections.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
265308
Name
Gommerman Jennifer L
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
IgA Plasma Cells: Where, How and What
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$726,000
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Activation Induced Cytidine Deaminase; Antibody; B Lymphocyte; Germinal Centre; Iga; Innate B Cells; Mucosal Tissues
Abstract
B lymphocytes are an important component of the immune system due to their ability to produce antibodies, molecules that can neutralize pathogens. Such antibody responses occur when B lymphocytes that are specific for the pathogen obtain help from pathogen-specific T lymphocytes. These cellular interactions take place within a complex microenvironment called the Germinal Centre which is located within lymph nodes or the spleen. However, it takes approximately one week to initiate a Germinal Centre response, and this puts the host at risk of succumbing to infection in the early days post-exposure. As a stop-gap, humans have an innate immune system that responds rapidly to microbial exposure. Interestingly, even though B and T lymphocytes are considered part of the adaptive immune system, some B and T lymphocytes have innate properties. This is particularly true in the mucosal tissues (gut, lung, reproductive tract) and in the skin, all of which are locations where pathogens first invade our bodies. We know much less about innate lymphocytes and how they participate in immune response compared to their adaptive counterparts. We are studying innate B cell responses, with particular focus on those innate responses that occur in the gut. In particular, we are interested in how innate B cells produce the mucosal antibody IgA, and whether IgA-secreting B cells may have special properties that allow them to fight off infections.
Competitiondate
201209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Gommerman, Jennifer L; Martin, Alberto
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $726,000~ $0~