Project Grant R01CA282027
- This Project Grant award of $663,340 from the National Cancer Institute (NCI), under the Cancer Biology Research federal grant program (CFDA 93.396), supports research to elucidate the mechanisms underlying regulatory T cell (Treg)-mediated suppression of tumor elimination by natural killer (NK) cells and CD4 T cells. The goal is to investigate how depletion of intratumoral Tregs can mobilize NK and CD4 T cells to control MHC I-deficient tumors that have escaped CD8 T cell responses. The...
- This $846,982 Project Grant award was provided by the National Cancer Institute (CFDA 93.396 Cancer Biology Research) to Beth Israel Deaconess Medical Center, Inc. (Bidmc) to conduct research aimed at understanding the role of immune checkpoint molecules like PD-1 in regulating myeloid cell differentiation and function in the tumor microenvironment. The goal is to identify new targets and strategies to enhance anti-tumor immunity and overcome barriers to cancer immunotherapy. The 7-year...
- This federal Project Grant award of $713,601.00 from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) aims to characterize the mechanisms by which defects in the homologous recombination (HR) DNA repair pathway influence the efficacy of immune checkpoint blockade therapies in cancer treatment. The primary objectives are to: 1) Elucidate the differential immunogenicity between BRCA2 and BRCA1 mutant tumors in murine models, 2) Evaluate whether differences in response to...
- This federal Project Grant award of $618,928 from the National Cancer Institute (CFDA 93.396 Cancer Biology Research) aims to investigate the role of regulatory T cells (Tregs) in suppressing antitumor immune responses within the tumor microenvironment and tumor-draining lymph nodes. The key objectives are to: Decipher the mechanisms by which Tregs control dendritic cell antigen uptake, which impacts T cell priming in the tumor-draining lymph nodes. Determine how altering antigen uptake...
- This Project Grant award from the National Cancer Institute (CFDA 93.395 - Cancer Treatment Research) provides $639,004 to Mayo Clinic from January 1, 2025 to December 31, 2029 to conduct research on using a novel long-acting interleukin-7 (NT-I7) in combination with anti-PD-1 checkpoint blockade for the treatment of glioblastoma. The key products and services to be delivered under this award include: Collecting and processing pre- and post-treatment tumor tissue and peripheral blood samples...
- This R03 project grant, awarded by the National Center for Advancing Translational Sciences (NCATS) under CFDA Program 93.350, aims to comprehensively identify metabolic enzymes that control the generation of TCF1+ progenitor CD8+ T cells, which are critical for durable anti-tumor immune responses. The $169,500 award, spanning from September 1, 2024 to August 31, 2026, will fund two key research objectives: Identifying metabolic enzymes whose loss alters T cell differentiation and the TCF1+...
- This $121,857 Project Grant award from the National Cancer Institute's Cancer Research Manpower program (CFDA 93.398) supports research at the University of Pittsburgh to systematically investigate how anti-cancer drugs modulate T cells in the tumor microenvironment. The key goals are to: (1) conduct in silico screening to identify anti-cancer drugs impacting T cell effector function, activation, stemness and proliferation; (2) perform single-cell CRISPR knockout screening to identify drug...
- This Project Grant award, valued at $1,419,108, was provided by the National Cancer Institute under the Cancer Treatment Research federal grant program (CFDA 93.395). The grant supports research to advance the understanding of how a novel neoadjuvant therapy, combining Pepinemab (an antibody that blocks Semaphorin 4D) with immune checkpoint blockade (Nivolumab and/or Ipilimumab), impacts the immune system in patients with solid tumors, using refractory melanoma as a model. Key findings from a...
- This Project Grant award from the National Cancer Institute (CFDA 93.398 - Cancer Research Manpower) to President and Fellows of Harvard College (Harvard Medical School) in the amount of $163,296 supports research to define the role of the cytokine IL-27 in promoting anti-tumor cytotoxic CD8+ T cell responses. The overarching goals are to: (1) determine the mechanisms by which IL-27 drives CD8+ T cell cytotoxicity against tumors, and (2) elucidate the regulation of IL-27 production. Through this...
- This Project Grant award from the National Cancer Institute (CFDA 93.398 - Cancer Research Manpower) provides $127,629 to Harvard T.H. Chan School of Public Health to elucidate the role of both germline and somatic human leukocyte antigen (HLA) variations in cellular immunity and the efficacy of immune checkpoint inhibitor monotherapy in patients with non-small cell lung cancer. The research aims to leverage multi-omic data (genetics, genomics, transcriptomics, proteomics) from over 80,000 NSCLC...
BHLHE40 REGULATION OF T CELL FUNCTION DURING CANCER IMMUNOTHERAPY - PROJECT SUMMARY/ABSTRACT FOR CANCER IMMUNOTHERAPIES SUCH AS IMMUNE CHECKPOINT THERAPY (ICT), SUCCESS DEPENDS ON SUSTAINED ACTIVATION OF INTRATUMORAL EFFECTOR T CELLS RECOGNIZING TUMOR ANTIGENS. WHILE MANY OF THE MOLECULAR CHANGES REQUIRED FOR EFFECTOR T CELLS TO CONTROL CANCER ARE KNOWN, MANY KEY EPIGENETIC AND TRANSCRIPTIONAL FEATURES REQUIRED FOR ICT-INDUCED ANTI-TUMOR IMMUNITY ARE UNKNOWN. WE RECENTLY FOUND IN PRECLINICAL SARCOMA AND MELANOMA MODELS THAT ANTI-PD-1 OR ANTI-CTLA-4 ICT INDUCES STRONG UPREGULATION OF THE TRANSCRIPTION FACTOR, BHLHE40, IN TUMOR ANTIGEN-SPECIFIC CD8 AND CD4 T CELLS, WHICH ARE CRUCIAL FOR ICT-INDUCED TUMOR REJECTION AND ELIMINATION. WE FURTHER DISCOVERED CONDITIONAL DELETION OF BHLHE40 IN CD4+ T REGULATORY CELLS (TREGS), CD4 T CELLS, AND CD8 T CELLS RENDERED MICE TREATED WITH ICT INCAPABLE OF REJECTING ICT-SENSITIVE TUMORS. BHLHE40- DEFICIENT CD4 AND CD8 T CELLS EXHIBITED NOTABLE REDUCTIONS IN ICT-DRIVEN INTERFERON GAMMA (IFN-G) PRODUCTION ASSOCIATED WITH DEFECTS IN ICT-INDUCED REMODELING OF INTRATUMORAL MACROPHAGES. GENE SET ENRICHMENT ANALYSIS INDICATED DYSREGULATED METABOLISM WITHIN CERTAIN SUBPOPULATIONS OF CD4+ AND CD8+ T CELLS IN THE ABSENCE OF BHLHE40. HOWEVER, THESE ANALYSES WERE DONE IN MICE LACKING BHLHE40 IN TREGS AND CONVENTIONAL CD4 AND CD8 T CELLS. THEREFORE, IT IS IMPORTANT TO DELINEATE HOW BHLHE40 CONTRIBUTES TO NOT ONLY CD8 BUT ALSO CD4 T CELL (WHICH ARE NOW ACKNOWLEDGED TO BE CRITICAL FOR EFFECTIVE ANTI-TUMOR IMMUNITY) EFFECTOR FUNCTION. WE WILL TEST THE CENTRAL HYPOTHESIS THAT BHLHE40 IS A PIVOTAL TRANSCRIPTIONAL REGULATOR OF BOTH CD4 AND CD8 T CELL ANTI-TUMOR EFFECTOR FUNCTION DURING ANTI-PD-1/ANTI-CTLA-4 ICT AND TUMOR-SPECIFIC CANCER VACCINE THERAPIES. IN AIM 1, WE WILL USE CONVENTIONAL CD4 OR CD8 T CELL-SPECIFIC BHLHE40 KNOCKOUT (KO) MICE, NEWLY GENERATED MOUSE MELANOMA MODELS THAT EXPRESS DEFINED NEOANTIGENS, AND MOUSE SARCOMA LINES TO DETERMINE HOW CELL- SPECIFIC DELETION OF BHLHE40 IMPACTS RESPONSE TO ANTI-PD-1 AND/OR ANTI-CTLA-4 ICT OR TUMOR-SPECIFIC NEOANTIGEN CANCER VACCINE TREATMENT. WE WILL THEN ANALYZE TUMORS FROM CD4 OR CD8 T CELL SPECIFIC BHLHE40 KO MICE AND BHLHE40 REPORTER MICE BY SINGLE CELL RNA SEQUENCING (SCRNASEQ), MASS CYTOMETRY (CYTOF), AND CODEX MULTIPLEX IMAGING, TO ASSESS HOW LOSS OF BHLHE40 IN CD4 OR CD8 T CELLS ALTERS THE IMMUNE TUMOR MICROENVIRONMENT. IN AIM 2, WE WILL DISSECT THE MECHANISM BY WHICH BHLHE40 REGULATES CD4 AND CD8 T CELL FUNCTION IN THE CONTEXT OF DIFFERENT IMMUNOTHERAPIES BY SEVERAL APPROACHES SUCH AS FUNCTIONAL ASSAYS, SINGLE- CELL SEQUENCING ASSAY FOR TRANSPOSASE-ACCESSIBLE CHROMATIN (SCATACSEQ), CHROMATIN IMMUNOPRECIPITATION SEQUENCING (CHIPSEQ), AND LUCIFERASE REPORTER ASSAYS. IN AIM 3, WE WILL RELATE OUR FINDINGS IN MICE TO HUMANS BY FIRST MANIPULATING THE EXPRESSION OF BHLHE40 IN HUMAN CD4 AND CD8 T CELLS TO DETERMINE HOW BHLHE40 REGULATES THEIR EFFECTOR FUNCTION AND THEN ANALYZING PRE- AND POST-ICT TREATMENT PATIENT SAMPLES. THESE STUDIES WILL CONTRIBUTE TO OUR UNDERSTANDING OF HOW T CELLS RECOGNIZING TUMOR ANTIGENS MAINTAIN EFFECTOR FUNCTIONS DURING ICT AND THERAPEUTIC NEOANTIGEN CANCER VACCINES AND COULD IDENTIFY BHLHE40 AS A NOVEL THERAPEUTIC TARGET.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $606.6k | 5/30/25 | ||
| Not listed | $606.6k | 5/30/24 |