PyroTIMER Technology: Enabling T-Cell Persistence in Immunosuppressive Tumor Microenvironments
Project Number1R44CA295355-01
Contact PI/Project LeaderBAGATI, ARCHIS
Awardee OrganizationPYROJAS INC
Description
Abstract Text
Abstract
The challenge of effectively treating cancer is further complicated by the limitations of current CAR-T cell
therapies, especially when confronted with the immunosuppressive tumor microenvironment (TIME). Central to
this issue is the transforming growth factor-beta (TGF-β), which induces T cell exhaustion and curtails their
antitumor potency. Current methodologies to inhibit the TGF-β pathway have yielded suboptimal results due to
transient effects. This project introduces PyroTIMER CAR-T cells, an innovative approach that promises durable
inhibition of all TGF-β isoforms within the TIME. This robust strategy not only targets TGF-β with unprecedented
potency but also incorporates multiple technical advancements, enhancing T cell cytotoxicity and leveraging
patient-derived xenograft (PDX) models for a more accurate representation of the tumor milieu.
The overarching research plan is to thoroughly assess PyroTIMER CAR-T cells in both immunocompetent
syngeneic models and PDX models. Employing multi-parametric flow cytometry, we aim to delve into the immune
dynamics within tumors, elucidating how PyroTIMER CAR-T cells interact with and potentially remodel the TIME.
Our objectives are four-fold: 1. Deciphering the influence of TGF-β on PyroTIMER CAR-T cells. 2. Profiling
cytokine production to gauge risks, particularly concerning cytokine release syndrome (CRS). 3. Investigating
potential exhaustion scenarios in PyroTIMER CAR-T cells. 4. In-depth in vivo evaluations of the safety and
efficacy of PyroTIMER CAR-T cells.
Our long-term trajectory is underpinned by a commitment to patient safety and therapeutic efficacy. By forging
collaborations with pharmaceutical entities, refining manufacturing strategies for scalability, and seeking FDA
endorsement, we aspire to position PyroTIMER CAR-T cells at the forefront of personalized cancer therapies.
This initiative represents a harmonious blend of advanced scientific inquiry, patient well-being, and strategic
commercial planning. Through this endeavor, we aim to redefine CAR-T cell therapy, presenting a novel, potent,
and safer treatment paradigm for cancer patients.
Public Health Relevance Statement
Narrative
Pyrojas has developed PyroTIMER CAR-T cells that express an anti-TGF-β fusion protein to enhance the
efficacy of CAR-T cell therapy by inhibiting the TGF-β pathway. In preliminary studies, PyroTIMER CD19 CAR-
T cells have demonstrated enhanced cytotoxicity and persistence compared to traditional CD19 CAR-T cells
against B cell lymphomas in cellular and animal models. The objective of this proposal is to evaluate the safety
and efficacy of PyroTIMER CAR-T cells in preclinical animal models of B-cell lymphoma, breast cancer, and lung
cancer. The study aims to provide critical preclinical safety and efficacy data to pave the way for further clinical
development of PyroTIMER CAR-T cells in treating human cancers where efficacy is limited by the
immunosuppressive TIME.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Adverse reactionsAftercareAnimal ModelAntigen TargetingB-Cell LymphomasBenchmarkingBiological AssayBioluminescenceBreast Cancer CellBreast MelanomaCAR T cell therapyCD19 geneCancer PatientCell LineCell ProliferationCell modelCellsChimeric ProteinsClinical TrialsCollaborationsCytolysisDataDevelopmentDoseEnsureEnvironmentEvaluationExhibitsFlow CytometryFutureHematologic NeoplasmsHumanImmuneImmune responseImmunocompetentImmunosuppressionIn VitroInfusion proceduresInvestigational New Drug ApplicationLong-Term EffectsLuciferasesMalignant Breast NeoplasmMalignant NeoplasmsMalignant neoplasm of lungMeasurementMeasuresMediatingMediatorMelanoma CellMethodologyMonitorMusOutcomePathway interactionsPatient-Focused OutcomesPatientsPeptidesPersonal SatisfactionPharmacologic SubstancePhasePopulationPositioning AttributePredispositionProductionProliferatingProtein IsoformsResearchRiskSafetyScientific Advances and AccomplishmentsScientific InquirySeriesSolid NeoplasmT cell therapyT-LymphocyteTCR ActivationTechnologyTestingTherapeuticTimeTissue StainsToxic effectTransforming Growth Factor betaTreatment EfficacyTumor BurdenTumor VolumeValidationXenograft Modelantitumor effectbioluminescence imagingburden of illnesscell killingchimeric antigen receptorchimeric antigen receptor T cellsclinical developmentcomparativecytokinecytokine release syndromecytotoxiccytotoxicitydesigndisorder controleffective therapyefficacy studyengineered T cellsexhaustionforgingimmunogenicimmunogenicityimprovedimproved outcomein vitro Assayin vivoin vivo evaluationinnovationmanufacturemouse modelnovelpatient derived xenograft modelpatient safetypersonalized cancer therapyphase 2 studypre-clinicalpreclinical efficacypreclinical safetyresiliencetherapy designtriple-negative invasive breast carcinomatumortumor microenvironmenttumor-immune system interactions
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