Newborns and young infants are at risk of infection and often respond sub-optimally to vaccines. HIPC Project 3 proposes to leverage two technological advances that will provide fundamental new insights into vaccine- induced molecular changes associated with protective immunity and may transform future neonatal vaccine development: 1) novel ?OMIC? technologies capable of measuring comprehensive molecular signatures, in particular transcriptomics and proteomics, following immunization; and 2) the development of human in vitro systems to model age-specific innate and adaptive immune responses to immunization. Our preliminary data suggest that vaccines currently given at birth, the Alum-adjuvanted hepatitis B vaccine (HBV) and the live attenuated Mycobacterium bovis named Bacille Calmette-Gurin (BCG), induce age-dependent immune and OMIC responses, and that these distinct in vivo-induced changes can also be modeled in vitro. Accordingly, the goal of Project 3 is to characterize age-specific OMIC responses to immunization in vitro and in vivo in well- defined cohorts to deepen our understanding of vaccine-induced signatures that predict vaccine immunogenicity, including correlates of protection (CoP), and enhance future age-specific vaccine development. We will achieve this goal by pursuing the following Specific Aims:
in Specific Aim 1, we will characterize vaccine-induced molecular pathways correlating with CoP in vivo employing whole blood assays in vitro; and in Specific Aim 2, we will characterize vaccine-induced molecular pathways correlating with CoP in vivo employing human microphysiologic tissue constructs in vitro HIPC Project 3 will work in synergy with the other HIPC components, including Projects-1 (OMIC integration) and -2 (Immunophenotyping) and the Data Management Core to define and validate signatures that correlate with neonatal vaccine immunogenicity. These studies will leverage novel in vitro platforms to define, characterize and dissect molecular signatures corresponding to newborn vaccine immunogenicity, thereby informing future early life vaccine development. !

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI118608-05
Application #
10063829
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2016-12-27
Project End
2021-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
5
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Boston Children's Hospital
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Scheid, Annette; Borriello, Francesco; Pietrasanta, Carlo et al. (2018) Adjuvant Effect of Bacille Calmette-Guérin on Hepatitis B Vaccine Immunogenicity in the Preterm and Term Newborn. Front Immunol 9:29
Lux, Markus; Brinkman, Ryan Remy; Chauve, Cedric et al. (2018) flowLearn: fast and precise identification and quality checking of cell populations in flow cytometry. Bioinformatics 34:2245-2253
Borriello, Francesco; van Haren, Simon D; Levy, Ofer (2018) First International Precision Vaccines Conference: Multidisciplinary Approaches to Next-Generation Vaccines. mSphere 3: