Please use this identifier to cite or link to this item:
http://doi.org/10.25358/openscience-227
Authors: | Zimmer, Niklas Kim, Ella Schupp, Jonathan Sprang, Bettina Leukel, Petra Khafaji, Fatemeh Ringel, Florian Sommer, Clemens Tüttenberg, Jochen Tüttenberg, Andrea |
Title: | GARP as an immune regulatory molecule in the tumor microenvironment of glioblastoma multiforme |
Online publication date: | 8-Nov-2019 |
Year of first publication: | 2019 |
Language: | english |
Abstract: | Glycoprotein A repetition predominant (GARP), a specific surface molecule of activated regulatory T cells, has been demonstrated to significantly contribute to tolerance in humans by induction of peripheral Treg and regulatory M2-macrophages and by inhibition of (tumorantigen specific) T effector cells. Previous work identified GARP on Treg, and also GARP on the surface of several malignant tumors, as well as in a soluble form being shedded from their surface, contributing to tumor immune escape. Preliminary results also showed GARP expression on brain metastases of malignant melanoma. On the basis of these findings, we investigated whether GARP is also expressed on primary brain tumors. We showed GARP expression on glioblastoma (GB) cell lines and primary GB tissue, as well as on low-grade glioma, suggesting an important influence on the tumor micromilieu and the regulation of immune responses also in primary cerebral tumors. This was supported by the finding that GB cells led to a reduced, in part GARP-dependent effector T cell function (reduced proliferation and reduced cytokine secretion) in coculture experiments. Interestingly, GARP was localized not only on the cell surface but also in the cytoplasmatic, as well as nuclear compartments in tumor cells. Our findings reveal that GARP, as an immunoregulatory molecule, is located on, as well as in, tumor cells of GB and low-grade glioma, inhibiting effector T cell function, and thus contributing to the immunosuppressive tumor microenvironment of primary brain tumors. As GARP is expressed on activated Treg, as well as on brain tumors, it may be an interesting target for new immunotherapeutic approaches using antibody-based strategies as this indication. |
DDC: | 610 Medizin 610 Medical sciences |
Institution: | Johannes Gutenberg-Universität Mainz |
Department: | FB 04 Medizin |
Place: | Mainz |
ROR: | https://ror.org/023b0x485 |
DOI: | http://doi.org/10.25358/openscience-227 |
URN: | urn:nbn:de:hebis:77-publ-594100 |
Version: | Published version |
Publication type: | Zeitschriftenaufsatz |
License: | CC BY |
Information on rights of use: | https://creativecommons.org/licenses/by/4.0/ |
Journal: | International journal of molecular sciences 20 15 |
Pages or article number: | Art. 3676 |
Publisher: | Molecular Diversity Preservation International |
Publisher place: | Basel |
Issue date: | 2019 |
ISSN: | 1422-0067 1661-6596 |
Publisher URL: | http://dx.doi.org/10.3390/ijms20153676 |
Publisher DOI: | 10.3390/ijms20153676 |
Appears in collections: | JGU-Publikationen |