Publications by authors named "Catharina Lotsch"

Meningiomas are the most common primary intracranial tumors in adults and typically have a slow-growing and benign nature. However, there is also a substantial subset of meningiomas that shows aggressive clinical behavior and is refractory to standard treatment modalities, which are still limited to surgery and/or radiotherapy. Despite intensive research, no systemic treatment options are yet available in the clinic for these challenging tumors, resulting in poor patient outcome.

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Personalized cancer immunotherapies such as therapeutic vaccines and adoptive transfer of T cell receptor-transgenic T cells rely on the presentation of tumor-specific peptides by human leukocyte antigen class I molecules to cytotoxic T cells. Such neoepitopes can for example arise from somatic mutations and their identification is crucial for the rational design of new therapeutic interventions. Liquid chromatography mass spectrometry (LC-MS)-based immunopeptidomics is the only method to directly prove actual peptide presentation and we have developed a parameter optimization workflow to tune targeted assays for maximum detection sensitivity on a per peptide basis, termed optiPRM.

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Glioblastoma is the most common primary brain cancer in adults and represents one of the worst cancer diagnoses for patients. Suffering from a poor prognosis and limited treatment options, tumor recurrences are virtually inevitable. Additionally, treatment resistance is very common for this disease and worsens the prognosis.

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Article Synopsis
  • - Targeting glioblastoma-associated macrophages and microglial cells (GAMs) can significantly enhance patient outcomes, particularly through the inhibition of the colony-stimulating factor-1 receptor (CSF1R).
  • - In experiments, three CSF1R-targeting drugs were tested on patient-derived GAMs, with GW2580 proving the most effective in reprogramming them to enhance anti-tumor immune responses and decrease tumor proliferation.
  • - GW2580 showed notable promise by promoting a pro-inflammatory GAM phenotype and supporting antitumor T-cell responses, indicating its potential as a key treatment in future glioblastoma therapies.
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