Immunomodulatory biomaterial to enhancing T-cell responses to triple negative breast cancer
Immunomodulatory biomaterial to enhancing T-cell responses to triple negative breast cancer
批准号:
10699815
负责人:
Fatemeh Sadat Majedi
金额:
$39.96万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
已结题
起止时间:
2023-05-01 至 2024-08-31
关键词:
4T1Abscopal effectAdjuvantAdverse effectsAffectAlginatesAntibodiesAutoimmuneBiocompatible MaterialsBiological SciencesBiomedical EngineeringBiopsyBreast Cancer ModelCAR T cell therapyCanis familiarisCaringCellsCertificationCessation of lifeClinical TrialsCytotoxic T-LymphocytesDataDevelopmentDevicesDistantDistant MetastasisDrug KineticsEarly treatmentEndowmentExonsFlow CytometryFormulationFundingGoalsHematologic NeoplasmsHistologyHumanImmuneImmune systemImmunityImmunologicsImmunotherapyImplantIn SituIncubatorsInfiltrationLoxP-flanked alleleLymphocyteLymphomaMalignant NeoplasmsMechanicsMetastatic breast cancerModalityMusMyelogenousNeoadjuvant TherapyNeoplasm MetastasisOperative Surgical ProceduresOutcomePerformancePhasePilot ProjectsPoriferaRattusRegulatory T-LymphocyteSecureSiteSolid NeoplasmT cell responseT-Cell ActivationT-LymphocyteTechniquesTestingTimeToxic effectTransforming Growth Factor betaTranslatingTumor SuppressionUnited StatesWorkarmbiocompatible polymerbiodegradable polymercancer infiltrating T cellschemotherapycytokine release syndromedesigneffector T cellengineered T cellsexhaustionexperiencefightingimmunoregulationimprovedinhibitorinnovationlymph nodesmalignant breast neoplasmmanufacturabilitymanufacturemelanomamouse modelneoplastic cellnovel therapeuticsparticlepatient derived xenograft modelpolyoma middle tumor antigenpre-Investigational New Drug meetingrecruitresponsescaffoldside effectstandard of caretriple-negative invasive breast carcinomatumortumor microenvironmenttumor-immune system interactions
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Project Summary
Deaths from solid tumors vastly outnumber deaths from hematopoietic cancers. Yet progress in
immunotherapies for solid tumors is well behind those for lymphoma. CAR-T cell therapies and
engineered T cells have become revolutionary approaches for hematopoietic cancers, but their
potential for solid tumors is yet to be realized. Significant challenges hinder the potential of
immune therapies in solid tumors, including insufficient activation and eventual exhaustion of
effector T cells; and suppression of T cell effector responses in the tumor microenvironment. In
this proposal we consider these hurdles and offer a biomaterial solution that overcomes them.
This proposal is significant in facilitating endogenous T cells to fight solid tumors. Surgery is a
major treatment modality for both invasive and in situ tumors, but at this time, there are no specific
immunotherapies initiated at the time of surgery; they all start days to weeks later. Our proposal
is significant for offering a way to start treatments early, right at the time of initial surgery. Here
our synthetic scaffold, SymphNode can be injected at the time of biopsy or surgery not to only
recruit and active tumor-experienced local immune cells but also to suppress the inhibitory cells
created by tumor cells. Our long-term goal is to develop this bioengineered, locally injected,
“synthetic lymph node” into a therapy for human tumors.
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