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partners*

Marc Schmitz 

Affiliation

Institute of Immunology, Faculty of Medicine Carl Gustav Carus, TU Dresden and Immune Monitoring Unit, National Center for Tumor Diseases Dresden,
Dresden, Germany 

Main scientific interest

The tumor immune architecture plays a critical role for the prognosis of patients (Binnewies M et al., Nat Med 2018;24:541-550, Bruni D et al., Nat Rev Cancer 2020;11:662-680). In addition, it can essentially contribute to the clinical efficacy of various treatment modalities, including immune checkpoint inhibitor therapy. In this context, the major current research topic of the Schmitz group is the comprehensive characterization of the tumor immune architecture by transcriptome profiling, multiparametric flow cytometry, multispectral imaging, and functional analysis (Vadakekolathu J et al., Sci Transl Med. 2020;12:eaaz0463, Kießler et al., J Immunother Cancer. 2021;9:e001813,  Tirado-Gonzalez I et al., Cancer Discov. 2021;11:2924-2943, Peuker K et al., Immunity. 2022;55:701-717). In particular, they explore the composition, frequency, spatial distribution, phenotype, functional orientation, and clinical relevance of various immune cell subsets in tumor tissues obtained prior to, during or after treatment by utilizing multispectral imaging. The main goals are to gain novel insights into the underlying mechanisms of therapeutic strategies, to discover potential modes of resistance to treatment, and to identify novel treatment-related prognostic and predictive biomarkers. In addition, the characterization of the tumor immune contexture may have implications for the design of novel immunotherapeutic strategies that improve the clinical outcome of cancer patients.

 

RiseBrain-related technologies

The main objectives of the RISEBrain consortium are to elucidate the immunosuppressive mechanisms in brain metastases to enhance anti-tumor immunity through targeted intervention and thus significantly improve the clinical response of patients to immunotherapy. In this context, the Schmitz group will perform a detailed characterisation of the immunosuppressive tumor microenvironment in brain metastases by utilizing the Vectra and MACSima imaging platforms. For this purpose, the frequency, spatial distribution, phenotype and functional properties of different immune cell populations in brain metastases of patients from retrospective and prospective cohorts will be analyzed. Furthermore, the tumor microenvironment in brain metastases from mice will be investigated in which targeted pharmacological intervention is intended to improve anti-tumor immunity.  

Most relevant awards and honors

Postdoctoral Scholarship, Novartis Foundation for Therapeutic Research

AACR-AFLAC Scholar in Training Award, American Association for Cancer Research

Travel Award, American Society of Hematology

Meet Marc Schmitz 

News & Outreach*

2023

Clinical studies (Immune monitoring performed by Schmitz group)

A phase II single arm clinical trial of a tailored immunotherapy approach with nivolumab in subjects with metastatic or advanced transitional cell carcinoma

2023

Clinical studies (Immune monitoring performed by Schmitz group)

A phase II single arm clinical trial of a tailored immunotherapy approach with nivolumab in subjects with metastatic or advanced renal cell carcinoma

2023

Characterization of the immune architecture and immunomodulatory capabilities of melanoma-derived brain metastases

Funding Organisation: Federal Ministry of Education and Research

2023

Grants

SaxoCell: Development of theranostic target molecules for diagnosis and therapy

Funding Organisation: Federal Ministry of Education and Research

Achievements*

Prophylactic transfer of BCR-ABL-, PR1-, and WT1-reactive donor T cells after T-cell-depleted allogeneic hematopoietic cell transplantation in patients with chronic myeloid leukemia

Blood

Tumor-infiltrating plasmacytoid dendritic cells are associated with survival in human colon cancer

J Immunother Cancer

Microbiota-dependent activation of the myeloid calcineurin-NFAT pathway inhibits B7H3- and B7H4-dependent anti-tumor immunity in colorectal cancer 

Immunity