Mechanism of innate and adaptive immune development in human neonates
We are experts in scaled down immunoassays to characterize the immunological phenotype of infants born between 24 weeks to full-term, and during the neonatal period. We employ both molecular and human cell-based immunology approaches. Our current focus is on the maturation of innate immune Pattern Recognition Receptor (PRR) pathways and on neonatal T cell differentiation.
To support research we developed the BC Women’s Hospital Preemie Biobank, the first biobank dedicated to infants born below 33 weeks of gestation in Canada, in partnership with the BC Children’s Hospital Biobank and the Women’s Health Research Institute (WHRI).
Immunity to natural viral exposure in high-risk newborns
RSV and influenza are two main causes of Lower Respiratory Tract Infection (LRTI) in young infants. Newborns are naïve to these viruses and less responsive to vaccines against influenza, the common cause of flu. In this study, we aim to understand how infants respond to active or passive immunization against common respiratory viruses in terms of their antibody responses.
Heritability of Bronchopulmonary Dysplasia (BPD)
BPD is a form of chronic inflammatory-mediated lung disease affecting thousands of infants born below 30 weeks of gestation each year in Canada. Clinicians lack a cure for BPD and current treatments can have serious side-effects. In this project, we study anti-inflammatory interventions and examine how genetic factors affect the regulation of inflammation and predispose infants to BPD.
Improving the early diagnosis of neonatal sepsis in Malawi
Sepsis (e.g. severe infections) is a main cause of mortality worldwide in low/middle outcome countries. Diagnosis of neonatal sepsis can be challenging in newborns due to the difficulty in recognizing warning signs especially for non-expert health workers. In this study, we aim to understand the clinical presentation and epidemiology of neonatal sepsis at Kamuzu Central Hospital in a main pediatric hospital center in Malawi. We also work to understand how host response immune signatures between infants with versus those without sepsis in order to improve diagnosis and medical management.