{"id":5736,"date":"2024-12-11T18:05:29","date_gmt":"2024-12-11T18:05:29","guid":{"rendered":"https:\/\/mnitf.org\/?page_id=5736"},"modified":"2024-12-11T18:05:29","modified_gmt":"2024-12-11T18:05:29","slug":"funded-grants-2020","status":"publish","type":"page","link":"https:\/\/mnitf.org\/es\/funded-grants-2020\/","title":{"rendered":"Funded Grants – 2020"},"content":{"rendered":"
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FUNDED GRANTS - 2020<\/h2>
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COLUMBIA UNIVERSITY MEDICAL CENTER<\/strong>\u200b<\/p>\n

Targeting HLA Antibodies with belatacept and a proteasome inhibitor in heart transplantation<\/em><\/p>\n

The primary objective of this study is to define functionally relevant, mechanistically driven biomarkers that predict and monitor response to a synergistic strategy targeting HLA antibodies with belatacept and a proteasome inhibitor. This will be accomplished by performing i) detailed immunophenotyping, ii) HLA antibody characterization, and iii) intragraft molecular assessment using gene expression profiling. The secondary objective is to use these findings to develop novel, precision-based therapeutic paradigms which can ultimately be tailored to the patient\u2019s underlying immunophenotype.<\/p>\n

Principal Investigator: Marlena Habal, MD
\nAwarded: September 2020
\nDuration: 12 months
\nAmount of Award: $75,000<\/p>\n

IVIVA MEDICAL, INC.<\/strong>\u200b<\/p>\n

Non-synthetic Lung-on-a-chip COVID-19 Model Platform<\/em>\u200b<\/p>\n

The overall goal is to provide fellow researchers with a viable model of lung epithelium useful for modeling novel viral infection, immune response, and discovery of therapeutic strategies. The Grantee proposes to use our biologic scaffold to establish long-term culture of a human 3D lung model and introduce perturbations (e.g., lipopolysaccharide) to validate the model. The proposed model will utilize human induced pluripotent stem cell (iPSC)-derived alveolar epithelial and endothelial cells.\u200b<\/p>\n

Principal Investigator: Daniel Cheng, MD
\nAwarded: September 2020
\nDuration:\u00a0 12 months
\nAmount of Award: $74,988<\/p>\n

UNIVERSITY OF CALIFORNIA, SAN FRANCISCO<\/strong><\/p>\n

SARS CoV-2-pseudotyped vectors for immune response evaluation and vaccine development<\/em><\/p>\n

The overall objective is to develop SARS-CoV-2 pseudotyped lentiviral vectors for use in antibody neutralization assays using human kidney and lung cells, for investigation of antibody-dependent modulation of immunocyte infection, and for evaluation as a multivalent vaccine platform.\u200b<\/p>\n

Principal Investigator: Noriyuki Kasahara, MD, PhD
\nAwarded: September 2020
\nDuration:\u00a0 12 months
\nAmount of Award: $82,500<\/p>\n

UNIVERSITY OF ALBERTA, EDMONTON<\/strong>\u200b<\/p>\n

SARS CoV-2-pseudotyped vectors for immune response evaluation and vaccine development<\/em>\u200b<\/p>\n

The main goal of INTERLUNG is to establish a precise and accurate system for diagnosing the rejection and chronic atrophy\/fibrosis states in lung transplant patients, focusing particularly on chronic lung allograft dysfunction (CLAD), using the Molecular Microscope\u00ae Diagnostic System (MMDx) platform that incorporates microarrays (and in some cases RNA sequencing) plus machine-learning\/AI approaches. This study aims to provide insight into the biology of CLAD and its relationship to rejection, and establish the clinical utility of the MMDx System as a precise and accurate diagnostic platform.<\/p>\n

Principal Investigator: Philip F. Halloran, MD, PhD
\nAwarded: March 2020
\nDuration:\u00a0 6 months
\nAmount of Award: $75,000<\/p>\n

MASSACHUSETTS GENERAL HOSPITAL<\/strong>\u200b<\/p>\n

Engineering of distal pulmonary epithelium from human iPSCs by recapitulating fetal lung development<\/em><\/p>\n

Building lungs for transplantation will require the generation of epithelial populations of well-defined developmental state, which is currently not defined or replicated by stem cell or developmental biology. To bridge this gap, Grantee will investigate neonatal human lung epithelium at single cell resolution and define transcriptome signatures, then utilize fetal developmental signals to induce formation of functional epithelium using induced pluripotent stem cells derived alveolar cells. Grantee will crosscheck engineered against native epithelium in comparative analyses and optimize the process.<\/p>\n

Principal Investigator: Tong Wu, PhD
\nAwarded: March 2020
\nDuration: 12 months
\nAmount of Award: $100,000<\/p>\n

COLUMBIA UNIVERSITY<\/strong>\u200b<\/p>\n

Genetic and Immune Predictors of Recurrent Glumerulonephritis of the Kidney Allograft<\/em><\/p>\n

Recurrent glomerulonephritis (GN) is a type of kidney disease that recurs after transplantation. Despite being a leading cause of kidney transplant failure, recurrent GN is poorly understood. Grantee hypothesizes that inherited and immune factors are needed to develop recurrent GN. To identify predictors of recurrent GN, Grantee will compare genetic and immunologic factors in kidney transplants patients with and without recurrent GN. This may lead to improve donor-recipient matching and discovery of more effective therapies. The goal is to reduce recurrent GN and improve kidney transplant survival.<\/p>\n

Principal Investigator: Ibrahim Batal, MD
\nAwarded: March 2020
\nDuration: 12 months
\nAmount of Award: $149,361<\/p>\n\n\t\t<\/div>\n\t<\/div>\n<\/div><\/div><\/div><\/div>

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