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Hattingen, E.

Publications and source records attributed to Hattingen, E..

2 recordsLinked to original sources

Absolute quantification of cerebral metabolites using 2D 1H-MRSI with quantitative MRI-based water reference

PurposeMetabolite concentrations are valuable biomarkers in brain tumors (BT). However, correction of water relaxation effects often requires time-consuming quantitative MRI (qMRI) sequences on top of a lengthy spectroscopic water reference acquisition. The goal of this work was to develop and validate a fast metabolite quantification method where a 2D spectroscopic water reference acquisition is obtained using a fast qMRI protocol and single-voxel STEAM sequence. MethodsA 2D sLASER sequence was acquired for MRSI. An 8-minute qMRI protocol was also acquired. A single-voxel unsuppressed water signal was acquired using a STEAM sequence. The H2O map, obtained from qMRI, was calibrated based on the STEAM-signal to obtain the spectroscopic water reference (proposed method). Five healthy volunteers and one BT patient were scanned at 3T. Concentrations obtained using the proposed and two reference methods, one where water relaxation effects were corrected using literature values (Reference method) and one where they were corrected using qMRI-derived values (Reference method with qMRI) were compared. ResultsIn healthy subjects, WM metabolite concentrations obtained using water relaxation using literature values (Reference method) significantly differed from those using individual-specific corrections (Reference method with qMRI and proposed method). Bland-Altman analyses revealed a very low bias and SD of the differences between the Reference method with qMRI and the proposed-method (Bias<0.5% and SD<10%). The BT regions showed a [~]15% underestimation of metabolite concentrations using the Reference method. ConclusionFor metabolite quantification, accurate water referencing with individual-specific corrections for water relaxation times was obtained in 8 minutes using the proposed method.

neuroscience↗

Glioma-associated tertiary lymphoid structures are sites of lymphocyte clonal expansion and plasma cell formation

Adult-type diffuse gliomas, the most common primary brain tumors, pose significant clinical challenges due to limited treatment options, restricted anti-tumor immune response and dismal patient prognosis. In this study, we elucidate the immunological function and clinical relevance of intra-tumoral tertiary lymphoid structures (TLS) in adaptive anti-glioma immunity. We conducted a comprehensive, unbiased analysis of lymphoid aggregation in 642 gliomas using a multi-modal approach that combines RNA sequencing with spatial transcriptome and proteome profiling. Our findings reveal that TLS are present in 15% of tumors and correlate with improved overall survival. Gliomas with TLS exhibit a remodeled perivascular space, marked by transcriptional upregulation and spatial redistribution of collagens associated with barrier functions. Furthermore, we demonstrate that TLS maturation into sites of dynamic adaptive immune responses, characterized by clonal T and B cell expansion and IgA+ and IgG+ plasma-cell formation, is driven by efficient early T cell recruitment to the perivascular space.

immunology↗