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Article ; Online: Stability and Maintenance of Foxp3

Korn, Thomas / Muschaweckh, Andreas

2019 Volume 10, Page(s) 2634

Abstract: ... ...

Abstract	Foxp3
MeSH term(s)	Animals ; Forkhead Transcription Factors/immunology ; Homeostasis/immunology ; Humans ; Inflammation/immunology ; T-Lymphocytes, Regulatory/immunology
Chemical Substances	Forkhead Transcription Factors
Language	English
Publishing date	2019-11-14
Publishing country	Switzerland
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Review
ZDB-ID	2606827-8
ISSN	1664-3224 ; 1664-3224
ISSN (online)	1664-3224
ISSN	1664-3224
DOI	10.3389/fimmu.2019.02634
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Article: Evaluation of the Effect of CD70 Co-Expression on CD8 T Cell Response in Protein-Prime MVA-Boost Vaccination in Mice.

Stephan, Ann-Sophie / Kosinska, Anna D / Mück-Häusl, Martin / Muschaweckh, Andreas / Jäger, Clemens / Röder, Natalie / Heikenwälder, Mathias / Dembek, Claudia / Protzer, Ulrike

Vaccines

2023 Volume 11, Issue 2

Abstract: Here, we investigate the potential of CD70 co-expression during viral vector boost vaccination to improve an antigen-specific T cell response. To determine the chance of activating antigen-specific T cells by CD70, we used the HBV core antigen as a model ...

Abstract	Here, we investigate the potential of CD70 co-expression during viral vector boost vaccination to improve an antigen-specific T cell response. To determine the chance of activating antigen-specific T cells by CD70, we used the HBV core antigen as a model antigen in a heterologous protein-prime, Modified Vaccinia virus Ankara (MVA) boost vaccination scheme. Both the HBV core and a CD70 expression cassette were co-expressed upon delivery by an MVA vector under the same promoter linked by a P2A site. To compare immunogenicity with and without CD70 co-expression, HBV-naïve, C57BL/6 (wt) mice and HBV-transgenic mice were prime-vaccinated using recombinant HBV core antigen followed by the MVA vector boost. Co-expression of CD70 increased the number of vaccine-induced HBV core-specific CD8 T cells by >2-fold and improved their effector functions in HBV-naïve mice. In vaccinated HBV1.3tg mice, the number and functionality of HBV core-specific CD8 T cells was slightly increased upon CD70 co-expression in low-viremic, but not in high-viremic animals. CD70 co-expression did not impact liver damage as indicated by ALT levels in the serum, but increased the number of vaccine-induced, proliferative T cell clusters in the liver. Overall, this study indicates that orchestrated co-expression of CD70 and a vaccine antigen may be an interesting and safe means of enhancing antigen-specific CD8 T cell responses using vector-based vaccines, although in our study it was not sufficient to break immune tolerance.
Language	English
Publishing date	2023-01-21
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2703319-3
ISSN	2076-393X
ISSN	2076-393X
DOI	10.3390/vaccines11020245
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Article ; Online: IL-1β and IL-23 Promote Extrathymic Commitment of CD27

Muschaweckh, Andreas / Petermann, Franziska / Korn, Thomas

Journal of immunology (Baltimore, Md. : 1950)

2017 Volume 199, Issue 8, Page(s) 2668–2679

Abstract: γδT17 cells are a subset of γδ T cells committed to IL-17 production and are characterized by the expression of IL-23R and CCR6 and lack of CD27 expression. γδT17 cells are believed to arise within a narrow time window during prenatal thymic development. ...

Abstract	γδT17 cells are a subset of γδ T cells committed to IL-17 production and are characterized by the expression of IL-23R and CCR6 and lack of CD27 expression. γδT17 cells are believed to arise within a narrow time window during prenatal thymic development. In agreement with this concept, we show in this study that adult
MeSH term(s)	Aminoquinolines ; Animals ; Cell Differentiation ; Cells, Cultured ; Disease Models, Animal ; Humans ; Imiquimod ; Interleukin-17/metabolism ; Interleukin-1beta/metabolism ; Interleukin-2 Receptor beta Subunit/metabolism ; Interleukin-23/metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Psoriasis/immunology ; Receptors, Antigen, T-Cell, gamma-delta/metabolism ; Receptors, Interleukin/genetics ; T-Lymphocytes/physiology ; Tumor Necrosis Factor Receptor Superfamily, Member 7/metabolism
Chemical Substances	Aminoquinolines ; Interleukin-17 ; Interleukin-1beta ; Interleukin-2 Receptor beta Subunit ; Interleukin-23 ; Receptors, Antigen, T-Cell, gamma-delta ; Receptors, Interleukin ; Tumor Necrosis Factor Receptor Superfamily, Member 7 ; interleukin-23 receptor, mouse ; Imiquimod (P1QW714R7M)
Language	English
Publishing date	2017-08-30
Publishing country	United States
Document type	Journal Article
ZDB-ID	3056-9
ISSN	1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
ISSN (online)	1550-6606
ISSN	0022-1767 ; 1048-3233 ; 1047-7381
DOI	10.4049/jimmunol.1700287
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Article ; Online: IL-23 stabilizes an effector T

Wertheimer, Tobias / Zwicky, Pascale / Rindlisbacher, Lukas / Sparano, Colin / Vermeer, Marijne / de Melo, Bruno Marcel Silva / Haftmann, Claudia / Rückert, Tamina / Sethi, Aakriti / Schärli, Stefanie / Huber, Anna / Ingelfinger, Florian / Xu, Caroline / Kim, Daehong / Häne, Philipp / Fonseca da Silva, André / Muschaweckh, Andreas / Nunez, Nicolas / Krishnarajah, Sinduya /

Köhler, Natalie / Zeiser, Robert / Oukka, Mohamed / Korn, Thomas / Tugues, Sonia / Becher, Burkhard

Nature immunology

2024 Volume 25, Issue 3, Page(s) 512–524

Abstract: Interleukin-23 (IL-23) is a proinflammatory cytokine mainly produced by myeloid cells that promotes tumor growth in various preclinical cancer models and correlates with adverse outcomes. However, as to how IL-23 fuels tumor growth is unclear. Here, we ... ...

Abstract	Interleukin-23 (IL-23) is a proinflammatory cytokine mainly produced by myeloid cells that promotes tumor growth in various preclinical cancer models and correlates with adverse outcomes. However, as to how IL-23 fuels tumor growth is unclear. Here, we found tumor-associated macrophages to be the main source of IL-23 in mouse and human tumor microenvironments. Among IL-23-sensing cells, we identified a subset of tumor-infiltrating regulatory T (T
MeSH term(s)	Animals ; Humans ; Mice ; Cytokines ; Interleukin-23/genetics ; Neoplasms/genetics ; T-Lymphocytes ; Tumor Microenvironment
Chemical Substances	Cytokines ; Interleukin-23
Language	English
Publishing date	2024-02-14
Publishing country	United States
Document type	Journal Article
ZDB-ID	2016987-5
ISSN	1529-2916 ; 1529-2908
ISSN (online)	1529-2916
ISSN	1529-2908
DOI	10.1038/s41590-024-01755-7
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Article ; Online: Cognate microglia-T cell interactions shape the functional regulatory T cell pool in experimental autoimmune encephalomyelitis pathology.

Haimon, Zhana / Frumer, Gal Ronit / Kim, Jung-Seok / Trzebanski, Sébastien / Haffner-Krausz, Rebecca / Ben-Dor, Shifra / Porat, Ziv / Muschaweckh, Andreas / Chappell-Maor, Louise / Boura-Halfon, Sigalit / Korn, Thomas / Jung, Steffen

Nature immunology

2022

Abstract: Microglia, the parenchymal brain macrophages of the central nervous system, have emerged as critical players in brain development and homeostasis. The immune functions of these cells, however, remain less well defined. We investigated contributions of ... ...

Abstract	Microglia, the parenchymal brain macrophages of the central nervous system, have emerged as critical players in brain development and homeostasis. The immune functions of these cells, however, remain less well defined. We investigated contributions of microglia in a relapsing-remitting multiple sclerosis paradigm, experimental autoimmune encephalitis in C57BL/6 x SJL F
Language	English
Publishing date	2022-12-01
Publishing country	United States
Document type	Journal Article
ZDB-ID	2016987-5
ISSN	1529-2916 ; 1529-2908
ISSN (online)	1529-2916
ISSN	1529-2908
DOI	10.1038/s41590-022-01360-6
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Article ; Online: IL-24 intrinsically regulates Th17 cell pathogenicity in mice.

Sie, Christopher / Kant, Ravi / Peter, Christian / Muschaweckh, Andreas / Pfaller, Monika / Nirschl, Lucy / Moreno, Helena Domínguez / Chadimová, Tereza / Lepennetier, Gildas / Kuhlmann, Tanja / Öllinger, Rupert / Engleitner, Thomas / Rad, Roland / Korn, Thomas

The Journal of experimental medicine

2022 Volume 219, Issue 8

Abstract: In certain instances, Th17 responses are associated with severe immunopathology. T cell-intrinsic mechanisms that restrict pathogenic effector functions have been described for type 1 and 2 responses but are less well studied for Th17 cells. Here, we ... ...

Abstract	In certain instances, Th17 responses are associated with severe immunopathology. T cell-intrinsic mechanisms that restrict pathogenic effector functions have been described for type 1 and 2 responses but are less well studied for Th17 cells. Here, we report a cell-intrinsic feedback mechanism that controls the pathogenicity of Th17 cells. Th17 cells produce IL-24, which prompts them to secrete IL-10. The IL-10-inducing function of IL-24 is independent of the cell surface receptor of IL-24 on Th17 cells. Rather, IL-24 is recruited to the inner mitochondrial membrane, where it interacts with the NADH dehydrogenase (ubiquinone) 1 α subcomplex subunit 13 (also known as Grim19), a constituent of complex I of the respiratory chain. Together, Grim19 and IL-24 promote the accumulation of STAT3 in the mitochondrial compartment. We propose that IL-24-guided mitochondrial STAT3 constitutes a rheostat to blunt extensive STAT3 deflections in the nucleus, which might then contribute to a robust IL-10 response in Th17 cells and a restriction of immunopathology in experimental autoimmune encephalomyelitis.
MeSH term(s)	Animals ; Cell Differentiation ; Cytokines/immunology ; Interleukin-10/metabolism ; Mice ; NADH, NADPH Oxidoreductases/metabolism ; Signal Transduction ; Th17 Cells ; Virulence
Chemical Substances	Cytokines ; Il24 protein, mouse ; Interleukin-10 (130068-27-8) ; NADH, NADPH Oxidoreductases (EC 1.6.-) ; Grim19 protein, mouse (EC 1.6.5.-)
Language	English
Publishing date	2022-07-12
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	218343-2
ISSN	1540-9538 ; 0022-1007
ISSN (online)	1540-9538
ISSN	0022-1007
DOI	10.1084/jem.20212443
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Article ; Online: Unrestrained cleavage of Roquin-1 by MALT1 induces spontaneous T cell activation and the development of autoimmunity.

Proceedings of the National Academy of Sciences of the United States of America

2023 Volume 120, Issue 48, Page(s) e2309205120

Abstract: Constitutive activation of the MALT1 paracaspase in conventional T cells ... ...

Abstract	Constitutive activation of the MALT1 paracaspase in conventional T cells of
MeSH term(s)	Mice ; Animals ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/genetics ; Autoimmunity ; Inflammation/metabolism ; Cell Differentiation ; Encephalomyelitis, Autoimmune, Experimental/genetics ; Receptors, Antigen, T-Cell/genetics ; Ubiquitin-Protein Ligases
Chemical Substances	Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein (EC 3.4.22.-) ; Receptors, Antigen, T-Cell ; Rc3h1 protein, mouse (EC 2.3.2.27) ; Ubiquitin-Protein Ligases (EC 2.3.2.27)
Language	English
Publishing date	2023-11-21
Publishing country	United States
Document type	Journal Article
ZDB-ID	209104-5
ISSN	1091-6490 ; 0027-8424
ISSN (online)	1091-6490
ISSN	0027-8424
DOI	10.1073/pnas.2309205120
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Article ; Online: B cells orchestrate tolerance to the neuromyelitis optica autoantigen AQP4.

Afzali, Ali Maisam / Nirschl, Lucy / Sie, Christopher / Pfaller, Monika / Ulianov, Oleksii / Hassler, Tobias / Federle, Christine / Petrozziello, Elisabetta / Kalluri, Sudhakar Reddy / Chen, Hsin Hsiang / Tyystjärvi, Sofia / Muschaweckh, Andreas / Lammens, Katja / Delbridge, Claire / Büttner, Andreas / Steiger, Katja / Seyhan, Gönül / Ottersen, Ole Petter / Öllinger, Rupert /

Rad, Roland / Jarosch, Sebastian / Straub, Adrian / Mühlbauer, Anton / Grassmann, Simon / Hemmer, Bernhard / Böttcher, Jan P / Wagner, Ingrid / Kreutzfeldt, Mario / Merkler, Doron / Pardàs, Irene Bonafonte / Schmidt Supprian, Marc / Buchholz, Veit R / Heink, Sylvia / Busch, Dirk H / Klein, Ludger / Korn, Thomas

Nature

2024 Volume 627, Issue 8003, Page(s) 407–415

Abstract: Neuromyelitis optica is a paradigmatic autoimmune disease of the central nervous system, in which the water-channel protein AQP4 is the target ... ...

Abstract	Neuromyelitis optica is a paradigmatic autoimmune disease of the central nervous system, in which the water-channel protein AQP4 is the target antigen
MeSH term(s)	Animals ; Humans ; Mice ; AIRE Protein ; Aquaporin 4/deficiency ; Aquaporin 4/genetics ; Aquaporin 4/immunology ; Aquaporin 4/metabolism ; Autoantibodies/immunology ; Autoantigens/immunology ; B-Lymphocytes/immunology ; B-Lymphocytes/metabolism ; CD40 Antigens/immunology ; Germinal Center/cytology ; Germinal Center/immunology ; Immune Tolerance ; Neuromyelitis Optica/immunology ; Neuromyelitis Optica/metabolism ; Receptors, Antigen, T-Cell/immunology ; T-Lymphocytes/immunology ; Thymus Gland/cytology ; Thymus Gland/immunology ; Thyroid Epithelial Cells/immunology ; Thyroid Epithelial Cells/metabolism ; Transcriptome
Chemical Substances	AIRE Protein ; AQP4 protein, human ; Aqp4 protein, mouse ; Aquaporin 4 ; Autoantibodies ; Autoantigens ; CD40 Antigens ; interleukin-21 (MKM3CA6LT1) ; Receptors, Antigen, T-Cell
Language	English
Publishing date	2024-02-21
Publishing country	England
Document type	Journal Article
ZDB-ID	120714-3
ISSN	1476-4687 ; 0028-0836
ISSN (online)	1476-4687
ISSN	0028-0836
DOI	10.1038/s41586-024-07079-8
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Article ; Online: Fetomaternal immune cross talk modifies T-cell priming through sustained changes to DC function.

Lacorcia, Matthew / Bhattacharjee, Sonakshi / Laubhahn, Kristina / Alhamdan, Fahd / Ram, Marija / Muschaweckh, Andreas / Potaczek, Daniel P / Kosinska, Anna / Garn, Holger / Protzer, Ulrike / Renz, Harald / Prazeres da Costa, Clarissa

The Journal of allergy and clinical immunology

2021 Volume 148, Issue 3, Page(s) 843–857.e6

Abstract: Background: Prenatal exposure to infections can modify immune development. These environmental disturbances during early life potentially alter the incidence of inflammatory disorders as well as priming of immune responses. Infection with the helminth ... ...

Abstract	Background: Prenatal exposure to infections can modify immune development. These environmental disturbances during early life potentially alter the incidence of inflammatory disorders as well as priming of immune responses. Infection with the helminth Schistosoma mansoni is widely studied for its ability to alter immune responsiveness and is associated with variations in coinfection, allergy, and vaccine efficacy in endemic populations. Objective: Exposure to maternal schistosomiasis during early life, even without transmission of infection, can result in priming effects on offspring immune responses to bystander antigenic challenges as related to allergic responsiveness and vaccination, with this article seeking to further clarify the effects and underlying immunologic imprinting. Methods: Here, we have combined a model of chronic maternal schistosomiasis infection with a thorough analysis of subsequent offspring immune responses to allergy and vaccination models, including viral challenge and steady-state changes to immune cell compartments. Results: We have demonstrated that maternal schistosomiasis alters CD4 Conclusion: In addition to steady-state modifications to CD4
MeSH term(s)	Allergens/immunology ; Animals ; B-Lymphocytes/immunology ; Cells, Cultured ; Dendritic Cells/immunology ; Female ; Fetus/immunology ; Gene Expression Profiling ; Immunization ; Lung/immunology ; Lymph Nodes/immunology ; Male ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Ovalbumin/immunology ; Pregnancy ; Prenatal Exposure Delayed Effects/immunology ; Respiratory Hypersensitivity/genetics ; Respiratory Hypersensitivity/immunology ; Schistosoma mansoni ; Schistosomiasis/immunology ; Spleen/immunology ; T-Lymphocytes/immunology ; Mice
Chemical Substances	Allergens ; Ovalbumin (9006-59-1)
Language	English
Publishing date	2021-03-05
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	121011-7
ISSN	1097-6825 ; 1085-8725 ; 0091-6749
ISSN (online)	1097-6825 ; 1085-8725
ISSN	0091-6749
DOI	10.1016/j.jaci.2021.02.031
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Article ; Online: Keratinocyte-intrinsic BCL10/MALT1 activity initiates and amplifies psoriasiform skin inflammation.

Kurgyis, Zsuzsanna / Vornholz, Larsen / Pechloff, Konstanze / Kemény, Lajos V / Wartewig, Tim / Muschaweckh, Andreas / Joshi, Abhinav / Kranen, Katja / Hartjes, Lara / Möckel, Sigrid / Steiger, Katja / Hameister, Erik / Volz, Thomas / Mellett, Mark / French, Lars E / Biedermann, Tilo / Korn, Thomas / Ruland, Jürgen

Science immunology

2021 Volume 6, Issue 65, Page(s) eabi4425

Abstract: Psoriasis is a chronic inflammatory skin disease arising from poorly defined pathological cross-talk between keratinocytes and the immune system. BCL10 (B cell lymphoma/leukemia 10) and MALT1 (mucosa-associated lymphoid tissue lymphoma translocation ... ...

Abstract	Psoriasis is a chronic inflammatory skin disease arising from poorly defined pathological cross-talk between keratinocytes and the immune system. BCL10 (B cell lymphoma/leukemia 10) and MALT1 (mucosa-associated lymphoid tissue lymphoma translocation protein 1) are ubiquitously expressed inflammatory signaling proteins that can interact with the psoriasis susceptibility factor CARD14, but their functions in psoriasis are insufficiently understood. We report that although keratinocyte-intrinsic BCL10/MALT1 deletions completely rescue inflammatory skin pathology triggered by germline
MeSH term(s)	Animals ; B-Cell CLL-Lymphoma 10 Protein/deficiency ; B-Cell CLL-Lymphoma 10 Protein/genetics ; B-Cell CLL-Lymphoma 10 Protein/immunology ; Female ; Inflammation/immunology ; Keratinocytes/immunology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/deficiency ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/genetics ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein/immunology ; Psoriasis/immunology ; Skin/immunology
Chemical Substances	B-Cell CLL-Lymphoma 10 Protein ; Bcl10 protein, mouse ; Malt1 protein, mouse (EC 3.4.22.-) ; Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein (EC 3.4.22.-)
Language	English
Publishing date	2021-11-26
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ISSN	2470-9468
ISSN (online)	2470-9468
DOI	10.1126/sciimmunol.abi4425
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