U19AI145825
Cooperative Agreement
Overview
Grant Description
Maternal Immunization and Determinants of Infant Immunity - Overall Abstract
Maternal Immunization and Determinants of Infant Immunity (MADI) aims to address the issue of infectious diseases, which continue to be the leading cause of death in children under 5 years old worldwide. Newborns and infants within the first year of life are particularly affected. The immune fitness of the mother plays a crucial role in the sustained health of a child. Vaccination during pregnancy has the potential to enhance maternal immunity and improve neonatal immunity to pathogens. However, there are still significant gaps in our understanding of how the unique immunological setting of pregnancy influences responses to vaccination, the rules of maternal antibody (AB) transfer, and the interactions between transferred maternal AB and the infant immune system.
To bridge this knowledge gap, MADI has proposed synergistic and multidisciplinary studies organized into three aims:
1. Distinguish unique features and predictors of vaccine-induced immunity during pregnancy.
2. Define the principles governing maternal antibody transfer.
3. Identify determinants of infant immunity and responses to vaccines.
MADI consists of four integrated and synergistic projects (P) and three cores (C):
P1 will determine the influence of pregnancy on AB biophysical and functional features, as well as B/T cell responses to vaccines.
P2 will identify AB-intrinsic factors underlying transfer via placenta and breast milk.
P3 will identify features of transferred maternal AB that mediate immunity to pathogens and regulate vaccine responses in infants.
P4 will identify cellular and molecular predictors of responses to vaccination in the mother-infant dyad.
C1 will provide cutting-edge systems serology and AB engineering technologies, training, and quality control.
C2 will provide centralized management and analysis of data from all projects and will manage data dissemination.
The Admin Core will provide management and programmatic support.
The MADI team combines complementary expertise, access to unique and well-characterized clinical cohorts, and state-of-the-art methods to dissect complex maternal-infant immune interactions. MADI has public health significance and translational value in:
1) Investigating the immunobiology of maternal immunization at a new breadth and depth.
2) Identifying novel actionable targets to improve the effectiveness of maternal immunization.
3) Informing vaccine design and implementation.
4) Stimulating the field of maternal-infant immunology and vaccinology by generating new analytical tools, mechanistic insights, and rich hypothesis-generating systems immunology datasets.
Such knowledge has the potential to transform the field of maternal immunization.
Maternal Immunization and Determinants of Infant Immunity (MADI) aims to address the issue of infectious diseases, which continue to be the leading cause of death in children under 5 years old worldwide. Newborns and infants within the first year of life are particularly affected. The immune fitness of the mother plays a crucial role in the sustained health of a child. Vaccination during pregnancy has the potential to enhance maternal immunity and improve neonatal immunity to pathogens. However, there are still significant gaps in our understanding of how the unique immunological setting of pregnancy influences responses to vaccination, the rules of maternal antibody (AB) transfer, and the interactions between transferred maternal AB and the infant immune system.
To bridge this knowledge gap, MADI has proposed synergistic and multidisciplinary studies organized into three aims:
1. Distinguish unique features and predictors of vaccine-induced immunity during pregnancy.
2. Define the principles governing maternal antibody transfer.
3. Identify determinants of infant immunity and responses to vaccines.
MADI consists of four integrated and synergistic projects (P) and three cores (C):
P1 will determine the influence of pregnancy on AB biophysical and functional features, as well as B/T cell responses to vaccines.
P2 will identify AB-intrinsic factors underlying transfer via placenta and breast milk.
P3 will identify features of transferred maternal AB that mediate immunity to pathogens and regulate vaccine responses in infants.
P4 will identify cellular and molecular predictors of responses to vaccination in the mother-infant dyad.
C1 will provide cutting-edge systems serology and AB engineering technologies, training, and quality control.
C2 will provide centralized management and analysis of data from all projects and will manage data dissemination.
The Admin Core will provide management and programmatic support.
The MADI team combines complementary expertise, access to unique and well-characterized clinical cohorts, and state-of-the-art methods to dissect complex maternal-infant immune interactions. MADI has public health significance and translational value in:
1) Investigating the immunobiology of maternal immunization at a new breadth and depth.
2) Identifying novel actionable targets to improve the effectiveness of maternal immunization.
3) Informing vaccine design and implementation.
4) Stimulating the field of maternal-infant immunology and vaccinology by generating new analytical tools, mechanistic insights, and rich hypothesis-generating systems immunology datasets.
Such knowledge has the potential to transform the field of maternal immunization.
Funding Goals
TO ASSIST PUBLIC AND PRIVATE NONPROFIT INSTITUTIONS AND INDIVIDUALS TO ESTABLISH, EXPAND AND IMPROVE BIOMEDICAL RESEARCH AND RESEARCH TRAINING IN INFECTIOUS DISEASES AND RELATED AREAS, TO CONDUCT DEVELOPMENTAL RESEARCH, TO PRODUCE AND TEST RESEARCH MATERIALS. TO ASSIST PUBLIC, PRIVATE AND COMMERCIAL INSTITUTIONS TO CONDUCT DEVELOPMENTAL RESEARCH, TO PRODUCE AND TEST RESEARCH MATERIALS, TO PROVIDE RESEARCH SERVICES AS REQUIRED BY THE AGENCY FOR PROGRAMS IN INFECTIOUS DISEASES, AND CONTROLLING DISEASE CAUSED BY INFECTIOUS OR PARASITIC AGENTS, ALLERGIC AND IMMUNOLOGIC DISEASES AND RELATED AREAS. PROJECTS RANGE FROM STUDIES OF MICROBIAL PHYSIOLOGY AND ANTIGENIC STRUCTURE TO COLLABORATIVE TRIALS OF EXPERIMENTAL DRUGS AND VACCINES, MECHANISMS OF RESISTANCE TO ANTIBIOTICS AS WELL AS RESEARCH DEALING WITH EPIDEMIOLOGICAL OBSERVATIONS IN HOSPITALIZED PATIENTS OR COMMUNITY POPULATIONS AND PROGRESS IN ALLERGIC AND IMMUNOLOGIC DISEASES. BECAUSE OF THIS DUAL FOCUS, THE PROGRAM ENCOMPASSES BOTH BASIC RESEARCH AND CLINICAL RESEARCH. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM EXPANDS AND IMPROVES PRIVATE SECTOR PARTICIPATION IN BIOMEDICAL RESEARCH. THE SBIR PROGRAM INTENDS TO INCREASE AND FACILITATE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. THE SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM STIMULATES AND FOSTERS SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. RESEARCH CAREER DEVELOPMENT AWARDS SUPPORT THE DEVELOPMENT OF SCIENTISTS DURING THE FORMATIVE STAGES OF THEIR CAREERS. INDIVIDUAL NATIONAL RESEARCH SERVICE AWARDS (NRSAS) ARE MADE DIRECTLY TO APPROVE APPLICANTS FOR RESEARCH TRAINING IN SPECIFIED BIOMEDICAL SHORTAGE AREAS. IN ADDITION, INSTITUTIONAL NATIONAL RESEARCH SERVICE AWARDS ARE MADE TO ENABLE INSTITUTIONS TO SELECT AND MAKE AWARDS TO INDIVIDUALS TO RECEIVE TRAINING UNDER THE AEGIS OF THEIR INSTITUTIONAL PROGRAM.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Baltimore,
Maryland
21201
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 403% from $3,188,570 to $16,036,849.
University Of Maryland, Baltimore was awarded
MADI: Maternal Immunization & Infant Immunity
Cooperative Agreement U19AI145825
worth $16,036,849
from the National Institute of Allergy and Infectious Diseases in July 2021 with work to be completed primarily in Baltimore Maryland United States.
The grant
has a duration of 4 years 9 months and
was awarded through assistance program 93.855 Allergy and Infectious Diseases Research.
The Cooperative Agreement was awarded through grant opportunity Administrative Supplements to Existing NIH Grants and Cooperative Agreements (Parent Admin Supp Clinical Trial Optional).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
7/12/21
Start Date
4/30/26
End Date
Funding Split
$16.0M
Federal Obligation
$0.0
Non-Federal Obligation
$16.0M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for U19AI145825
Transaction History
Modifications to U19AI145825
Additional Detail
Award ID FAIN
U19AI145825
SAI Number
U19AI145825-4161369926
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Funding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Awardee UEI
Z9CRZKD42ZT1
Awardee CAGE
1B0S2
Performance District
MD-07
Senators
Benjamin Cardin
Chris Van Hollen
Chris Van Hollen
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Institute of Allergy and Infectious Diseases, National Institutes of Health, Health and Human Services (075-0885) | Health research and training | Grants, subsidies, and contributions (41.0) | $6,233,295 | 100% |
Modified: 9/24/25