Simone Stupia

ORCID: 0000-0002-0961-5736
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About
Contact & Profiles
Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Cytokine Signaling Pathways and Interactions
  • Cutaneous Melanoma Detection and Management
  • CAR-T cell therapy research
  • interferon and immune responses
  • Bacterial Infections and Vaccines
  • T-cell and B-cell Immunology
  • Bacteriophages and microbial interactions
  • Melanoma and MAPK Pathways
  • Streptococcal Infections and Treatments
  • Redox biology and oxidative stress
  • Nanoplatforms for cancer theranostics
  • Pneumonia and Respiratory Infections

University of Duisburg-Essen
2022-2023

Deutschen Konsortium für Translationale Krebsforschung
2021-2022

German Cancer Research Center
2022

Düsseldorf University Hospital
2021

Heinrich Heine University Düsseldorf
2021

University of Trento
2018-2019

Bacterial outer membrane vesicles (OMVs) represent an interesting vaccine platform for their built-in adjuvanticity and simplicity of production process. Moreover, OMVs can be decorated with foreign antigens using different synthetic biology approaches. However, the optimal OMV engineering strategy, which should guarantee compartmentalization most heterologous in quantities high enough to elicit protective immune responses, remains validated. In this work we exploited lipoprotein transport...

10.1073/pnas.1905112116 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2019-10-07

Recent studies have demonstrated HLA class II (HLA-II)-dependent killing of melanoma cells by cytotoxic CD4 T cells. We investigated evolution HLA-II-loss tumors that escape T-cell activity and contribute to immunotherapy resistance.Melanoma from longitudinal metastases were studied for constitutive IFN-inducible HLA-II expression, sensitivity towards autologous cells, immune evasion loss. Clinical significance HLA-II-low was determined analysis transcriptomic data sets patients with...

10.1158/1078-0432.ccr-23-0099 article EN Clinical Cancer Research 2023-05-18

Drug-tolerant persister cells (DTPs) exhibit remarkable cell state heterogeneity and phenotypic evolvability. However, the central question of how DTPs epigenetically coordinate their metabolic flexibility to adapt early therapeutic stress remains unanswered. We have recently shown that histone demethylase KDM5B, which is intrinsically expressed in differentiated melanoma DTPs, reprograms landscape. exact mechanism by KDM5B affects underlying enzymes, whether this reveals new druggable...

10.1101/2025.03.10.641595 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2025-03-13

Human FAT1 is overexpressed on the surface of most colorectal cancers (CRCs) and in particular a 25 amino acid sequence (D8) present one 34 cadherin extracellular repeats carries epitope recognized by mAb198.3, monoclonal antibody which partially protects mice from challenge with human CRC cell lines xenograft mouse models. Here we data immune competent demonstrating potential D8-FAT1 as cancer vaccine. We first demonstrated that homolog (mD8-FAT1) also expressed CT26 B16F10 murine lines....

10.3389/fonc.2018.00481 article EN cc-by Frontiers in Oncology 2018-10-26

Background Immune-stimulatory agents, like agonists of the innate immune receptor RIG-I, are currently tested in clinical trials as an intratumoral treatment option for patients with unresectable melanoma, aiming to enhance anti-tumor T cell responses. Switching melanoma toward a dedifferentiated state has recently been linked and therapy resistance. It remains be determined whether RIG-I affect differentiation, potentially leading Methods Patient metastases-derived lines were treated...

10.1136/jitc-2021-003863 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2022-06-01

<div>AbstractPurpose:<p>Recent studies have demonstrated HLA class II (HLA-II)–dependent killing of melanoma cells by cytotoxic CD4 T cells. We investigated evolution HLA-II–loss tumors that escape T-cell activity and contribute to immunotherapy resistance.</p>Experimental Design:<p>Melanoma from longitudinal metastases were studied for constitutive IFN-inducible HLA-II expression, sensitivity towards autologous cells, immune evasion loss. Clinical significance...

10.1158/1078-0432.c.6700316.v2 preprint EN 2023-08-01

<div>Abstract<p>Purpose: Recent studies have demonstrated HLA class II (HLA-II)-dependent killing of melanoma cells by cytotoxic CD4 T cells. We investigated evolution HLA-II-loss tumors that escape cell activity and contribute to immunotherapy resistance. Experimental Design: Melanoma from longitudinal metastases were studied for constitutive interferon-inducible HLA-II expression, sensitivity towards autologous cells, immune evasion loss. Clinical significance HLA-II-low was...

10.1158/1078-0432.c.6700316.v3 preprint EN 2024-09-16

<div>Abstract<p>Purpose: Recent studies have demonstrated HLA class II (HLA-II)-dependent killing of melanoma cells by cytotoxic CD4 T cells. We investigated evolution HLA-II-loss tumors that escape cell activity and contribute to immunotherapy resistance. Experimental Design: Melanoma from longitudinal metastases were studied for constitutive interferon-inducible HLA-II expression, sensitivity towards autologous cells, immune evasion loss. Clinical significance HLA-II-low was...

10.1158/1078-0432.c.6700316 preprint EN 2023-06-16
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