Pieter J. Schol

ORCID: 0000-0002-9118-1630
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • Immune cells in cancer
  • Neuroblastoma Research and Treatments
  • CAR-T cell therapy research
  • PARP inhibition in cancer therapy
  • Genomics and Chromatin Dynamics
  • Prostate Cancer Treatment and Research
  • Inflammation biomarkers and pathways
  • IL-33, ST2, and ILC Pathways
  • Phagocytosis and Immune Regulation
  • T-cell and B-cell Immunology
  • interferon and immune responses

Leiden University Medical Center
2022-2024

Oncode Institute
2022-2024

Dana-Farber Cancer Institute
2022

The Netherlands Cancer Institute
2022

Activation of the stimulator interferon genes (STING) pathway promotes antitumor immunity but STING agonists have yet to achieve clinical success. Increased understanding mechanism action in human tumors is key developing therapeutic combinations that activate effective innate immunity. Here, we report malignant pleural mesothelioma cells robustly express and are responsive agonist treatment ex vivo. Using dynamic single-cell RNA sequencing explants treated with a agonist, observed CXCR3...

10.1158/2326-6066.cir-22-0017 article EN Cancer Immunology Research 2022-06-02

Abstract Androgen receptor (AR) drives prostate cancer (PCa) development and progression. AR chromatin binding profiles are highly plastic form recurrent programmatic changes that differentiate disease stages, subtypes patient outcomes. While prior studies focused on concordance between subgroups, inter-tumor heterogeneity of enhancer selectivity remains unexplored. Here we report high levels in human primary tumors, overlap with observed healthy epithelium. Such has functional consequences,...

10.1038/s41467-022-35135-2 article EN cc-by Nature Communications 2022-11-30

Human natural killer (NK) cells in lymphoid tissues can be categorized into three subsets: CD56brightCD16+, CD56dimCD16+ and CD69+CXCR6+ tissue-resident (lt)NK cells. How the subsets are functionally developmentally related is currently unknown. Therefore, we performed single-cell RNA sequencing combined with oligonucleotide-conjugated antibodies against CD56, CXCR6, CD117 CD34 on fresh bone marrow NK A minor CD56dimGzmK+ subset was identified that shared features CD56bright CD56dimGzmK-...

10.3389/fimmu.2022.1044398 article EN cc-by Frontiers in Immunology 2022-11-24

<div>Abstract<p>Activation of the stimulator interferon genes (STING) pathway promotes antitumor immunity but STING agonists have yet to achieve clinical success. Increased understanding mechanism action in human tumors is key developing therapeutic combinations that activate effective innate immunity. Here, we report malignant pleural mesothelioma cells robustly express and are responsive agonist treatment <i>ex vivo</i>. Using dynamic single-cell RNA sequencing...

10.1158/2326-6066.c.6550907.v1 preprint EN 2023-04-04

<div>Abstract<p>Activation of the stimulator interferon genes (STING) pathway promotes antitumor immunity but STING agonists have yet to achieve clinical success. Increased understanding mechanism action in human tumors is key developing therapeutic combinations that activate effective innate immunity. Here, we report malignant pleural mesothelioma cells robustly express and are responsive agonist treatment <i>ex vivo</i>. Using dynamic single-cell RNA sequencing...

10.1158/2326-6066.c.6550907 preprint EN 2023-04-04
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