TY  - JOUR
A1  - Ruck, Tobias
A1  - Bittner, Stefan
A1  - Afzali, Ali Maisam
A1  - Göbel, Kerstin
A1  - Glumm, Sarah
A1  - Kraft, Peter
A1  - Sommer, Claudia
A1  - Kleinschnitz, Christoph
A1  - Preusse, Corinna
A1  - Stenzel, Werner
A1  - Wiendl, Heinz
A1  - Meuth, Sven G.
T1  - The NKG2D-IL-15 signaling pathway contributes to T-cell mediated pathology in inflammatory myopathies
JF  - Oncotarget
N2  - NKG2D is an activating receptor on T cells, which has been implicated in the pathogenesis of autoimmune diseases. T cells are critically involved in idiopathic inflammatory myopathies (IIM) and have been proposed as specific therapeutic targets. However, the mechanisms underlying T cell-mediated progressive muscle destruction in IIM remain to be elucidated. We here determined the involvement of the NKG2D - IL-15 signaling pathway. Primary human myoblasts expressed NKG2D ligands, which were further upregulated upon inflammatory stimuli. In parallel, shedding of the soluble NKG2D ligand MICA (sMICA) decreased upon inflammation potentially diminishing inhibition of NKG2D signaling. Membrane-related expression of IL-15 by myoblasts induced differentiation of naive CD8\(^+\) T cells into highly activated, cytotoxic \(CD8^+NKG2D^{high}\) T cells demonstrating NKG2D-dependent lysis of myoblasts in vitro. \(CD8^+NKG2D^{high}\) T cell frequencies were increased in the peripheral blood of polymyositis (PM) patients and correlated with serum creatinine kinase concentrations, while serum sMICA levels were not significantly changed. In muscle biopsy specimens from PM patients expression of the NKG2D ligand MICA/B was upregulated, IL-15 was expressed by muscle cells, CD68\(^+\) macrophages as well as CD4\(^+\) T cells, and \(CD8^+NKG2D^+\) cells were frequently detected within inflammatory infiltrates arguing for a local signaling circuit in the inflammatory muscle milieu. In conclusion, the NKG2D - IL-15 signaling pathway contributes to progressive muscle destruction in IIM potentially opening new therapeutic avenues.
KW  - MIC ligands
KW  - pathology section
KW  - T cell activation
KW  - idiopathic inflammatory myopathies
KW  - polymyositis
KW  - IL-15
KW  - NKG2D
KW  - receptor
KW  - expression
KW  - lymphokine-activated killer
KW  - human muscle-cells
KW  - multiple sclerosis
KW  - celiac disease
KW  - tumor immunity
KW  - NKG2D ligands
KW  - cutting edge
Y1  - 2015
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-136047
VL  - 6
IS  - 41
ER  - 
TY  - JOUR
A1  - Zeiner, Pia S.
A1  - Preusse, Corinna
A1  - Golebiewska, Anna
A1  - Zinke, Jenny
A1  - Iriondo, Ane
A1  - Muller, Arnaud
A1  - Kaoma, Tony
A1  - Filipski, Katharina
A1  - Müller-Eschner, Monika
A1  - Bernatz, Simon
A1  - Blank, Anna-Eva
A1  - Baumgarten, Peter
A1  - Ilina, Elena
A1  - Grote, Anne
A1  - Hansmann, Martin L.
A1  - Verhoff, Marcel A.
A1  - Franz, Kea
A1  - Feuerhake, Friedrich
A1  - Steinbach, Joachim P.
A1  - Wischhusen, Jörg
A1  - Stenzel, Werner
A1  - Niclou, Simone P.
A1  - Harter, Patrick N.
A1  - Mittelbronn, Michel
T1  - Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
JF  - Brain Pathology
N2  - While the central nervous system is considered an immunoprivileged site and brain tumors display immunosuppressive features, both innate and adaptive immune responses affect glioblastoma (GBM) growth and treatment resistance. However, the impact of the major immune cell population in gliomas, represented by glioma-associated microglia/macrophages (GAMs), on patients’ clinical course is still unclear. Thus, we aimed at assessing the immunohistochemical expression of selected microglia and macrophage markers in 344 gliomas (including gliomas from WHO grade I–IV). Furthermore, we analyzed a cohort of 241 IDH1R132H-non-mutant GBM patients for association of GAM subtypes and patient overall survival. Phenotypical properties of GAMs, isolated from high-grade astrocytomas by CD11b-based magnetic cell sorting, were analyzed by immunocytochemistry, mRNA microarray, qRT-PCR and bioinformatic analyses. A higher amount of CD68-, CD163- and CD206-positive GAMs in the vital tumor core was associated with beneficial patient survival. The mRNA expression profile of GAMs displayed an upregulation of factors that are considered as pro-inflammatory M1 (eg, CCL2, CCL3L3, CCL4, PTGS2) and anti-inflammatory M2 polarization markers (eg, MRC1, LGMN, CD163, IL10, MSR1), the latter rather being associated with phagocytic functions in the GBM microenvironment. In summary, we present evidence that human GBMs contain mixed M1/M2-like polarized GAMs and that the levels of different GAM subpopulations in the tumor core are positively associated with overall survival of patients with IDH1R132H-non-mutant GBMs.
KW  - glioma
KW  - glioma-associated microglia and macrophages;
KW  - immune polarization
KW  - tumor microenvironment
Y1  - 2019
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-233897
VL  - 29
ER  -