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Compartmentalized inflammatory processes within the CNS might be a driver of tissue damage in chronic stages of CNS autoimmunity. Tissue resident T cells constitute a sizeable population of immune cells in the chronically inflamed CNS. However, little is known about their functional integration into CNS tissue niches. Here, we have identified the co-inhibitory molecule CD96 to be expressed on a subset of CNS resident conventional and regulatory T cells. Using genetic tools, we aim to investigate the interaction of CD96 with its CNS-expressed ligands and interrogate its function as a checkpoint to control perpetuation vs resolution of CNS resident T cell populations in the chronically inflamed CNS.
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Created: 6th Jul 2026 at 12:37
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Projects: CRC1002: Modulatory Units in Heart Failure, TRR 274: Checkpoints of Central Nervous System Recovery, SFB 1190: Compartmental Gates and Contact Sites in Cells
Web page: Not specified
https://rdp.sfb274.de/ (Research Data Platform) https://gepris.dfg.de/gepris/projekt/408885537 (DFG Gepris entry) The central nervous system (CNS) is a terminally differentiated tissue, where any insult carries a heightened risk - yet the tissue response to these insults is variable and can range from irreversible destruction to almost complete recovery. The rules that instruct these divergent outcomes are still unknown. The aim of this CRC is therefore to understand the biology of the multicellular ...
Programme: Sonderforschungsbereiche/Collaborative Research Centers
Public web page: https://www.sfb274.de/
Multidimensional single cell-analyses of T cells have fueled the debate about either extensive plasticity or “mixed” priming of T helper cell subsets in vivo. Here, we developed an experimental framework to probe the idea that the site of priming in the systemic immune compartment is a determinant of T helper cell-induced immunopathology in remote organs. By site-specific in vivo labeling of antigen-specific T cells in inguinal (i) or gut draining mesenteric (m) lymph nodes, we show that i-T cells ...
Submitter: Camilla Giudici
Investigation: A01 - CD96 as checkpoint for the persistence of...
Assays: Expression profiling: Bulk RNA-seq (mouse), Expression profiling: scRNA-seq (human), Expression profiling: scRNA-seq (mouse), Genome binding/occupancy profiling: Bulk ATAC-seq (mouse)
Snapshots: No snapshots
Submitter: Camilla Giudici
Assay type: Transcriptomics
Technology type: Sequencing
Investigation: A01 - CD96 as checkpoint for the persistence of...
Submitter: Camilla Giudici
Assay type: Transcriptomics
Technology type: Sequencing
Investigation: A01 - CD96 as checkpoint for the persistence of...
Organisms: Mouse
SOPs: No SOPs
Data files: Tracking of CD4+ T cells during CNS autoimmunity
Snapshots: No snapshots
Submitter: Camilla Giudici
Assay type: Gene Expression Profiling
Technology type: Rna-seq
Investigation: A01 - CD96 as checkpoint for the persistence of...
Organisms: Mouse
SOPs: No SOPs
Data files: Skin and gut imprinted T helper cell subsets ex...
Snapshots: No snapshots
Submitter: Camilla Giudici
Assay type: Experimental Assay Type
Technology type: Technology Type
Investigation: A01 - CD96 as checkpoint for the persistence of...
Organisms: Mouse
SOPs: No SOPs
Data files: Skin and gut imprinted T helper cell subsets ex...
Snapshots: No snapshots
Comparison of DNA accessibility by Omni-ATAC-seq in sorted effector i- and m-T cells (mD2RED CD4+ CD44high) and naive i- and m-T cells (mD2RED CD4+ CD44int) from spleen
Creators: None
Submitter: Camilla Giudici
We sorted i- and m-T cells (mD2REDCD4+CD44high) from lymph nodes and spleens of 2D2 x TH PhamT mice and performed RNAseq
Creators: None
Submitter: Camilla Giudici
Creators: None
Submitter: Camilla Giudici
Investigations: A01 - CD96 as checkpoint for the persistence of...
Single-cell transcriptome profiling of disease-related lymphocytes in patients with multiple sclerosis
Creators: None
Submitter: Camilla Giudici
Investigations: A01 - CD96 as checkpoint for the persistence of...
Abstract
Authors: Michael Hiltensperger, Eduardo Beltrán, Ravi Kant, Sofia Tyystjärvi, Gildas Lepennetier, Helena Domínguez Moreno, Isabel J. Bauer, Simon Grassmann, Sebastian Jarosch, Kilian Schober, Veit R. Buchholz, Selin Kenet, Christiane Gasperi, Rupert Öllinger, Roland Rad, Andreas Muschaweckh, Christopher Sie, Lilian Aly, Benjamin Knier, Garima Garg, Ali M. Afzali, Lisa Ann Gerdes, Tania Kümpfel, Sören Franzenburg, Naoto Kawakami, Bernhard Hemmer, Dirk H. Busch, Thomas Misgeld, Klaus Dornmair, Thomas Korn
Date Published: 7th Jun 2021
Publication Type: Journal Article
DOI: 10.1038/s41590-021-00948-8
Citation: Nat Immunol 22(7):880-892.
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https://orcid.org/0000-0002-3633-0955