Grant: CIHR Fellowship
Direct Payment
$225,000.00
Characterizing the Vaginal Antifungal Immune Response in the Context of Health and Diabetes
FY 2024-25
Summary
Despite impacting half of the global population, we currently lack a detailed understanding of how the immune system plays a role in vaginal health and disease. Our current knowledge indicates that immunity is different in the vagina compared to other sites in the body, demonstrating the importance of studying how the immune system specifically functions at the vaginal mucosa. Improving our understanding of vaginal immunity can provide important context relevant to the treatment of infections, cancers, fertility disorders, and other diseases of the female reproductive tract. To expand our understanding of vaginal immunity, I will be studying one of the most common diseases of the vagina, vulvovaginal candidiasis (VVC), commonly known as a yeast infection. About 75% of people with vaginas will experience VVC in their lifetime, and the risk factors are exceedingly common, including the use of antibacterials and both type-1 and type-2 diabetes. However, despite the commonality of VVC, we do not understand how the vagina fights the infection and why common illnesses like diabetes make people with vaginas more likely to develop the disease. Using multiple mouse models of diabetes, I have recapitulated this increased risk for VVC, and can now mechanistically dissect how the vagina combats infection, and how diabetes alters this fundamental immunology. Using immunology-based techniques, I will therefore characterize which components of the immune system are important for these responses to expand our understanding of vaginal immunology and pave the way for potential therapeutic interventions for VVC that target the immune system.
Department
Program
CIHR Fellowship
Recipient
Location
Maryland, United States of America
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
513402
Name
MacAlpine Jessie
Region
Maryland
Country
United States of America
Orgtype
Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Characterizing the Vaginal Antifungal Immune Response in the Context of Health and Diabetes
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$225,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Candida Albicans; Diabetes; Fungal Infection; Fungal Pathogenesis; Mucosal Immunology; Vaginal Candidiasis; Vaginal Immunology
Abstract
Despite impacting half of the global population, we currently lack a detailed understanding of how the immune system plays a role in vaginal health and disease. Our current knowledge indicates that immunity is different in the vagina compared to other sites in the body, demonstrating the importance of studying how the immune system specifically functions at the vaginal mucosa. Improving our understanding of vaginal immunity can provide important context relevant to the treatment of infections, cancers, fertility disorders, and other diseases of the female reproductive tract. To expand our understanding of vaginal immunity, I will be studying one of the most common diseases of the vagina, vulvovaginal candidiasis (VVC), commonly known as a yeast infection. About 75% of people with vaginas will experience VVC in their lifetime, and the risk factors are exceedingly common, including the use of antibacterials and both type-1 and type-2 diabetes. However, despite the commonality of VVC, we do not understand how the vagina fights the infection and why common illnesses like diabetes make people with vaginas more likely to develop the disease. Using multiple mouse models of diabetes, I have recapitulated this increased risk for VVC, and can now mechanistically dissect how the vagina combats infection, and how diabetes alters this fundamental immunology. Using immunology-based techniques, I will therefore characterize which components of the immune system are important for these responses to expand our understanding of vaginal immunology and pave the way for potential therapeutic interventions for VVC that target the immune system.
Competitiondate
202410
Approvedterm2
3 yrs 0 mth
Pinamesdelim
MacAlpine, Jessie
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $225,000~ $0~