We are pleased to announce that 50 investigators, from across BMC and the BU Medical & Charles River campuses, applied to the Integrated Pilot Award Program, sponsored by the BU Clinical and Translational Science Institute. From our pool of applications, 10 outstanding pilot projects were selected for funding, totaling an allocation of $373,600. We congratulate all of the recipients and look forward to their impactful contributions to translational research. |
| |
Placental Repository to Improve Infant Lung Outcomes in Preeclampsia | Through the PRIME study, Dr. Taglauer will seek to identify unique signaling proteins from preeclamptic placentas that are connected with pathways of lung and gut developmental injury. The study will also be creating a highly valuable biorepository of preeclamptic placental samples that will be available for collaborative studies. |
| |
Validity, Acceptability, and Utility of Electronic Health Record
Household Linking
| In this project, the team plans to evaluate how effective household linkage tools are by interviewing patients about their household membership, and cross-referencing their descriptions of household composition with household membership gathered through electronic health record linking. They will focus on a key disease that clusters within families, but for which there are few family-level care options: latent tuberculosis infection. |
| |
A soft-Foldable Robotic Retractor with Integrated Pressure Sensing to Reduce Tissue Trauma in Neurosurgery and Skull Base Surgery |
This pilot project will focus on the design, development, and evaluation of a novel soft robotic neurosurgical retractor to tackle current clinical barriers in neurological surgery and skull base surgery. The proposed system is designed to facilitate neurosurgery by creating a minimally invasive surgical workspace in the brain (through expansion and unfolding of pneumatically driven origami-inspired
soft robotic actuators) and monitor robot/tissue interaction (via soft capacitive pressure sensors).
|
| |
Self-Amplifying RNA Mediated Immunoglobulin Delivery for the Treatment
of Breast Cancer
| The goal of this project is to leverage a novel self-amplifying RNA (saRNA) technology developed by the Grinstaff and Wong lab to deliver an antibody for the treatment of breast cancer. Success from our work could provide better control of HER2-positive breast cancer progression by reducing tumor volume and extending survival compared to direct intravenous injection of chemotherapy. |
| |
A Soft Robotic Catheter for Percutaneous Management of Non-compressible Torso Hemorrhage | This project focuses on developing a novel device to enable controllable occlusion of the aorta to allow stabilization of the hemorrhage without completely cutting off blood flow to the lower extremities.The device will be designed to provide a safer alternative to current devices for management of non-compressible hemorrhage. It will be easy to use by enabling automation of the hemorrhage control process via robotic technologies. |
| |
Developing a Family-Based Program to Enhance Autonomy in Adults
with Down Syndrome
|
The current project focuses on improving daily quality of life of adults with Down syndrome. The team will use a community-engaged qualitative approach to develop an online family-based program to promote autonomy in adults with
Down syndrome. They will use a community-engaged qualitative approach to develop an online family-based program to promote autonomy in adults with Down syndrome. Building on prior work by our multidisciplinary research team, they will develop Project REACH (Ready to Enhance Autonomy in the Community and Home) – a community-based short-term program, delivered via telehealth, individualized for each family, and focused on skill-building.
|
| |
Radiation Therapy Resistance Promoted by LSD1 in Oral Cancer | The study showed that only 20-30% of tumors respond to RT. Thus, there is an unmet clinical need to identify radiosensitizers. The team has identified an epigenetic regulator, Lysine-specific demethylase 1 (LSD1), which promotes oral and resistance to RT. They expect to evaluate the novel mechanisms that LSD1 promotes DNA damage repair response signaling pathways and inhibition, which could promote sensitivity to RT using a mouse model and pathway analysis. |
| |
Dialysis Modality Education Access for Latinx Individuals
with Kidney Disease
|
Pre-dialysis kidney disease education is associated with significantly higher odds
of patient-centered preparation for dialysis amongst Latinx individuals. However, Latinx people are less likely to receive adequate kidney dialysis education prior
to dialysis, and are more likely to report lack of shared decision-making with
their clinician.The aim of this study is to 1) qualitatively evaluate the dialysis modality education experience for Latinx people with kidney disease and their clinicians and 2) establish a community research steering committee to co-design culturally tailored dialysis modality educational materials for Latinx individuals
with kidney disease.
|
| |
In-depth Profiling of Sickle Cell Disease (SCD) Hematopoietic Stem and Progenitor Cells (HSPCs) to Advance Gene Therapy and Transplantation Approaches | Sickle cell disease is associated with chronic inflammation of the bone marrow, affecting HSPCs residing in that niche. To better understand how this inflammation impacts their function and expression profile, the team will perform an in-depth characterization of SCD HSPCs, combining functional, transcriptional and cell surface profiling. This work will form the basis for an updated clinical workflow, enabling more accurate stem cell quantification. |
| |
Cardiopulmonary Biomarkers of Systemic Sclerosis | In this proposal, the team will investigate the role of cardiac disease using an advanced imaging approach, termed speckle-tracking echocardiography, that measures subclinical myocardial deformation to identify and create a library of associated protein biomarkers in the blood. The goal is to unravel potential mechanistic pathways to explain cardiac contributors to pulmonary hypertension for determining why these patients have such poor clinical outcomes. |
| |
| |
For information about our awardees and their Integrated Pilot Grant Award Projects
| | | | | |