Laura Joachim

ORCID: 0000-0003-2132-7013
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About
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Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Cancer Research and Treatments
  • CRISPR and Genetic Engineering
  • Phagocytosis and Immune Regulation
  • interferon and immune responses
  • Immune Cell Function and Interaction
  • Extracellular vesicles in disease
  • Gut microbiota and health
  • Immune cells in cancer
  • Cell death mechanisms and regulation
  • Click Chemistry and Applications
  • Clinical Nutrition and Gastroenterology

Technical University of Munich
2023-2025

Inter-individual differences in response to immune checkpoint inhibitors (ICI) remain a major challenge cancer treatment. The composition of the gut microbiome has been associated with differential ICI outcome, but underlying molecular mechanisms unclear, and therapeutic modulation challenging.

10.1016/j.ebiom.2023.104834 article EN cc-by-nc-nd EBioMedicine 2023-10-20

Tumor-derived extracellular vesicles (EVs) have been associated with immune evasion and tumor progression. We show that the RNA-sensing receptor RIG-I within cells governs biogenesis immunomodulatory function of EVs. Cancer-intrinsic activation releases EVs, which mediate dendritic cell maturation T antitumor immunity, synergizing checkpoint blockade. Intact RIG-I, autocrine interferon signaling, GTPase Rab27a in are required for immunostimulatory Active intrinsic signaling composition EV...

10.1016/j.xcrm.2023.101171 article EN cc-by-nc-nd Cell Reports Medicine 2023-08-31

Changes in the intestinal microbiome and microbiota-derived metabolites predict clinical outcomes after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Here, we report that desaminotyrosine (DAT), a product of bacterial flavonoid metabolism, correlates with improved overall survival reduced relapse rates allo-HSCT patients. In preclinical mouse models, treatment synthetic DAT prevents graft-versus-host disease by protecting barrier promoting regeneration contributes to...

10.1101/2025.04.08.647747 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2025-04-15

Background Immune checkpoint inhibitors (ICIs) of programmed cell death protein-1 (PD-1) or cytotoxic T-lymphocytes-associated protein 4 (CTLA-4) reinvigorate strong polyclonal T-cell immune responses against tumor cells. For many patients, these therapies fail because the development spontaneous is often compromised, as microenvironment (TME) lacks proinflammatory signals resulting in suboptimal activation antigen-presenting cells (APCs). Necroptosis a special form associated with leakage...

10.1136/jitc-2024-010433 article EN cc-by-nc-nd Journal for ImmunoTherapy of Cancer 2025-05-01

Summary Intestinal stem cells (ISC) promote tissue repair after genotoxic or immune-mediated injury. However, ISCs are particularly sensitive to various stressors and primary targets of overwhelming immune responses such as interferon-γ (IFNγ)-mediated killing. In mouse models gut damage biopsies from patients having undergone allo-hematopoietic cell transplantation, we observed IFNy expression by intestinal T reg cells. leverage combined IFNγ interleukin 10 (IL-10) stimulation nurture the...

10.1101/2024.10.21.617518 preprint EN 2024-10-24

Background: Inter-individual differences in response to immune checkpoint inhibitors (ICI) remain a major challenge cancer treatment. The composition of the gut microbiome has been associated with differential ICI outcome, but underlying molecular mechanisms unclear, and therapeutic modulation challenging.Methods: We established an vivo model treat mice type‑I interferon (IFN-I)-modulating, bacterial-derived metabolite desaminotyrosine (DAT) order improve therapy. Broad spectrum antibiotics...

10.2139/ssrn.4449685 preprint EN 2023-01-01
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