Giuseppina Astone

ORCID: 0000-0003-4206-3491
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About
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Research Areas
  • CAR-T cell therapy research
  • Immunotherapy and Immune Responses
  • Cancer Immunotherapy and Biomarkers
  • Lymphoma Diagnosis and Treatment
  • Prostate Cancer Treatment and Research
  • Biosimilars and Bioanalytical Methods
  • T-cell and Retrovirus Studies
  • Silk-based biomaterials and applications
  • Chronic Lymphocytic Leukemia Research
  • Acute Lymphoblastic Leukemia research
  • Immune Cell Function and Interaction
  • Antimicrobial Peptides and Activities

New York Hospital Queens
2025

Presbyterian Hospital
2025

NewYork–Presbyterian Hospital
2025

Cornell University
2021-2025

University of Genoa
2021-2023

Weill Cornell Medicine
2021-2023

Peripheral T cell lymphomas (PTCLs) comprise heterogeneous malignancies with limited therapeutic options. To uncover targetable vulnerabilities, we generate a collection of PTCL patient-derived tumor xenografts (PDXs) retaining histomorphology and molecular donor-tumor features over serial xenografting. PDX demonstrates remarkable heterogeneity, complex intratumor architecture, stepwise trajectories mimicking primary evolutions. Combining functional transcriptional stratification...

10.1016/j.xcrm.2025.102029 article EN cc-by-nc-nd Cell Reports Medicine 2025-03-01

Abstract Debate is around the optimal immunization regimen for cancer vaccines since too intense vaccination schedules may exhaust reactive lymphocytes. GX301 a telomerase-based vaccine whose safety and immunological effects were tested in phase I trial applying an eight administrations schedule. Main objective of this study was to comparatively analyse response three regimens metastatic castration-resistant prostate patients with response/disease stability after docetaxel chemotherapy. This...

10.1007/s00262-021-03024-0 article EN cc-by Cancer Immunology Immunotherapy 2021-08-05

Head and neck squamous cell carcinoma (HNSCC) has a poor clinical outcome despite the presence of rich CD8+ T tumor infiltrate in majority patients. This may be due to alterations infiltrating cells. Here, we performed characterization HNSCC cells cohort 30 The results showed that differential intratumoral frequency CD8+CD28+ cells, CD8+CD28− CD8+CD28−CD127−CD39+ Treg distinguished between patients who did or not respond treatment. Moreover, high PD1 expression identified subpopulation,...

10.3390/cancers13092234 article EN Cancers 2021-05-06

Background The current challenge for immunotherapies is to generate effective antitumor immunity. Since tumor immune escape mechanisms do not impact pre-existing and consolidated responses, we tested the hypothesis of redirecting a pregenerated immunity cancer: recall non-tumor antigen response against tumor, silk fibroin nanoparticles (SFNs) have been selected as ‘Trojan-horse’ carriers, promoting uptake by cells. Methods SFNs loaded with either ovalbumin (OVA) or CpG oligonucleotide (CpG)...

10.1136/jitc-2022-005916 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2023-01-01

T-cell lymphomas (TCLs) comprise a heterogeneous group of malignancies. Current therapeutic options remain limited, partly given the scarcity representative preclinical models. To uncover targetable vulnerabilities, we created collection TCL patient-derived-tumor-xenografts (PDXs) retaining molecular and histomorphology donor tumor features over serial xeno-grafting while capturing their mechanisms lymphomagenesis evolution. Ex-vivo cultures in-vivo experiments demonstrated remarkable...

10.2139/ssrn.4529648 preprint EN 2023-01-01
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