R01HD108015
Project Grant
Overview
Grant Description
Mechanisms of Innate Immune Dysfunction in SIV/Malaria Co-infection in Pregnancy - Project Summary/Abstract
HIV remains one of the world's most devastating diseases, with more than 38 million people living with HIV (PLWH) and an additional 1.7 million new infections per year. Moreover, in 2019, infection with malaria was reported to have reached 229 million cases worldwide and caused over 409,000 deaths. Although advances have been made in reducing the incidence of both HIV and malaria, the risk of infection with either disease is still great, especially in resource-limited countries. Importantly, the geographical overlap in endemic HIV and malaria constitutes a high risk for co-infection, fueling transmission and pathogenesis of both diseases.
The burdens of HIV and malaria are particularly elevated in pregnant women, leading to increased risk of poor birth outcomes and maternal and infant mortality. Notably, malaria in pregnancy (MIP) in women living with HIV (WLH) results in even greater risk of adverse outcomes, and the treatments currently available for MIP have only shown limited success in WLH. Therefore, our long-term goal is to identify key factors in MIP immunopathogenesis to aid in the development of new therapeutics that can safely and effectively reduce maternal and fetal morbidity and mortality in WLH.
The overall objectives for this application are to (1) dissect the pathogenic outcomes of P. fragile infection in SIV+ pregnant rhesus macaques (RMs) and (2) mechanistically elucidate the role of neutrophils and innate lymphoid cells (ILCs) in decidual inflammation during SIV/P. fragile co-infection. Our central hypothesis is that P. fragile and SIV co-infection of pregnant RMs will result in greater placental parasitemia and dysfunction that associates with higher levels of decidual neutrophil accumulation and ILC activation, as compared to mono-infected or healthy RMs.
The rationale for the proposed research is that a better understanding of the complex interplay of neutrophils and ILCs in placental dysfunction will promote subsequent, targeted studies to leverage our findings to develop novel interventions to treat MIP in WLH. The central hypothesis will be tested by pursuing three specific aims: 1) to identify key pathogenic consequences of P. fragile infection and the impact of SIV co-infection during pregnancy; 2) to define the role of neutrophils in peripheral and decidual inflammation during co-infection of pregnant RMs; and 3) to determine the role of ILCs in regulating peripheral and decidual inflammation in co-infected pregnant RMs.
The proposed research is innovative because it focuses on using a highly translational animal model to open new scientific horizons on key alterations in innate immune function that drive poor maternal and fetal outcomes in SIV and P. fragile co-infection, which closely parallels the dynamics of HIV and P. falciparum infection. The proposed research is significant because it is expected to provide a strong, evidence-based foundation for future pre-clinical studies of the biological mechanisms of MIP in WLH. Ultimately, these studies will provide new opportunities to develop therapies and prevention strategies to reduce morbidity and mortality due to malaria in highly vulnerable WLH.
HIV remains one of the world's most devastating diseases, with more than 38 million people living with HIV (PLWH) and an additional 1.7 million new infections per year. Moreover, in 2019, infection with malaria was reported to have reached 229 million cases worldwide and caused over 409,000 deaths. Although advances have been made in reducing the incidence of both HIV and malaria, the risk of infection with either disease is still great, especially in resource-limited countries. Importantly, the geographical overlap in endemic HIV and malaria constitutes a high risk for co-infection, fueling transmission and pathogenesis of both diseases.
The burdens of HIV and malaria are particularly elevated in pregnant women, leading to increased risk of poor birth outcomes and maternal and infant mortality. Notably, malaria in pregnancy (MIP) in women living with HIV (WLH) results in even greater risk of adverse outcomes, and the treatments currently available for MIP have only shown limited success in WLH. Therefore, our long-term goal is to identify key factors in MIP immunopathogenesis to aid in the development of new therapeutics that can safely and effectively reduce maternal and fetal morbidity and mortality in WLH.
The overall objectives for this application are to (1) dissect the pathogenic outcomes of P. fragile infection in SIV+ pregnant rhesus macaques (RMs) and (2) mechanistically elucidate the role of neutrophils and innate lymphoid cells (ILCs) in decidual inflammation during SIV/P. fragile co-infection. Our central hypothesis is that P. fragile and SIV co-infection of pregnant RMs will result in greater placental parasitemia and dysfunction that associates with higher levels of decidual neutrophil accumulation and ILC activation, as compared to mono-infected or healthy RMs.
The rationale for the proposed research is that a better understanding of the complex interplay of neutrophils and ILCs in placental dysfunction will promote subsequent, targeted studies to leverage our findings to develop novel interventions to treat MIP in WLH. The central hypothesis will be tested by pursuing three specific aims: 1) to identify key pathogenic consequences of P. fragile infection and the impact of SIV co-infection during pregnancy; 2) to define the role of neutrophils in peripheral and decidual inflammation during co-infection of pregnant RMs; and 3) to determine the role of ILCs in regulating peripheral and decidual inflammation in co-infected pregnant RMs.
The proposed research is innovative because it focuses on using a highly translational animal model to open new scientific horizons on key alterations in innate immune function that drive poor maternal and fetal outcomes in SIV and P. fragile co-infection, which closely parallels the dynamics of HIV and P. falciparum infection. The proposed research is significant because it is expected to provide a strong, evidence-based foundation for future pre-clinical studies of the biological mechanisms of MIP in WLH. Ultimately, these studies will provide new opportunities to develop therapies and prevention strategies to reduce morbidity and mortality due to malaria in highly vulnerable WLH.
Funding Goals
TO CONDUCT AND SUPPORT LABORATORY RESEARCH, CLINICAL TRIALS, AND STUDIES WITH PEOPLE THAT EXPLORE HEALTH PROCESSES. NICHD RESEARCHERS EXAMINE GROWTH AND DEVELOPMENT, BIOLOGIC AND REPRODUCTIVE FUNCTIONS, BEHAVIOR PATTERNS, AND POPULATION DYNAMICS TO PROTECT AND MAINTAIN THE HEALTH OF ALL PEOPLE. TO EXAMINE THE IMPACT OF DISABILITIES, DISEASES, AND DEFECTS ON THE LIVES OF INDIVIDUALS. WITH THIS INFORMATION, THE NICHD HOPES TO RESTORE, INCREASE, AND MAXIMIZE THE CAPABILITIES OF PEOPLE AFFECTED BY DISEASE AND INJURY. TO SPONSOR TRAINING PROGRAMS FOR SCIENTISTS, DOCTORS, AND RESEARCHERS TO ENSURE THAT NICHD RESEARCH CAN CONTINUE. BY TRAINING THESE PROFESSIONALS IN THE LATEST RESEARCH METHODS AND TECHNOLOGIES, THE NICHD WILL BE ABLE TO CONDUCT ITS RESEARCH AND MAKE HEALTH RESEARCH PROGRESS UNTIL ALL CHILDREN, ADULTS, FAMILIES, AND POPULATIONS ENJOY GOOD HEALTH. THE MISSION OF THE NICHD IS TO ENSURE THAT EVERY PERSON IS BORN HEALTHY AND WANTED, THAT WOMEN SUFFER NO HARMFUL EFFECTS FROM REPRODUCTIVE PROCESSES, AND THAT ALL CHILDREN HAVE THE CHANCE TO ACHIEVE THEIR FULL POTENTIAL FOR HEALTHY AND PRODUCTIVE LIVES, FREE FROM DISEASE OR DISABILITY, AND TO ENSURE THE HEALTH, PRODUCTIVITY, INDEPENDENCE, AND WELL-BEING OF ALL PEOPLE THROUGH OPTIMAL REHABILITATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Covington,
Louisiana
704338915
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 455% from $842,028 to $4,672,308.
The Administrators Of Tulane Educational Fund was awarded
Innate Immune Dysfunction in SIV/Malaria Co-infection during Pregnancy
Project Grant R01HD108015
worth $4,672,308
from the National Institute of Child Health and Human Development in September 2021 with work to be completed primarily in Covington Louisiana United States.
The grant
has a duration of 4 years 10 months and
was awarded through assistance program 93.865 Child Health and Human Development Extramural Research.
The Project Grant was awarded through grant opportunity Stephen I. Katz Early Stage Investigator Research Project Grant (R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
9/24/21
Start Date
7/31/26
End Date
Funding Split
$4.7M
Federal Obligation
$0.0
Non-Federal Obligation
$4.7M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01HD108015
Additional Detail
Award ID FAIN
R01HD108015
SAI Number
R01HD108015-1664383455
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NT00 NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development
Funding Office
75NT00 NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development
Awardee UEI
XNY5ULPU8EN6
Awardee CAGE
1BHK1
Performance District
LA-01
Senators
Bill Cassidy
John Kennedy
John Kennedy
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Child Health and Human Development, National Institutes of Health, Health and Human Services (075-0844) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,632,945 | 100% |
Modified: 9/24/25