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  1. Artikel: RelB+ Steady-State Migratory Dendritic Cells Control the Peripheral Pool of the Natural Foxp3+ Regulatory T Cells

    Reizis, Boris / Lutz, Manfred B.

    Frontiers in immunology, 8:726

    2017  

    Abstract: Thymus-derived natural Foxp3+ CD4+ regulatory T cells (nTregs) play a key role in maintaining immune tolerance and preventing autoimmune disease. Several studies indicate that dendritic cells (DCs) are critically involved in the maintenance and ... ...

    Körperschaft Leibniz-Institut für Alternsforschung
    Abstract Thymus-derived natural Foxp3+ CD4+ regulatory T cells (nTregs) play a key role in maintaining immune tolerance and preventing autoimmune disease. Several studies indicate that dendritic cells (DCs) are critically involved in the maintenance and proliferation of nTregs. However, the mechanisms how DCs manage to keep the peripheral pool at constant levels remain poorly understood. Here, we describe that the NF-κB/Rel family transcription factor RelB controls the frequencies of steady-state migratory DCs (ssmDCs) in peripheral lymph nodes and their numbers control peripheral nTreg homeostasis. DC-specific RelB depletion was investigated in CD11c-Cre × RelBfl/fl mice (RelBDCko), which showed normal frequencies of resident DCs in lymph nodes and spleen while the subsets of CD103− Langerin− dermal DCs (dDCs) and Langerhans cells but not CD103+ Langerin+ dDC of the ssmDCs in skin-draining lymph nodes were increased. Enhanced frequencies and proliferation rates were also observed for nTregs and a small population of CD4+ CD44high CD25low memory-like T cells (Tml). Interestingly, only the Tml but not DCs showed an increase in IL-2-producing capacity in lymph nodes of RelBDCko mice. Blocking of IL-2 in vivo reduced the frequency of nTregs but increased the Tml frequencies, followed by a recovery of nTregs. Taken together, by employing RelBDCko mice with increased frequencies of ssmDCs our data indicate a critical role for specific ssmDC subsets for the peripheral nTreg and IL-2+ Tml frequencies during homeostasis.
    Schlagwörter IL-2 ; RelB ; dendritic cells ; lymph nodes ; regulatory T cells
    Sprache Englisch
    Dokumenttyp Artikel
    Datenquelle Fachrepositorium Lebenswissenschaften

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  2. Artikel ; Online: Comments on the ambiguity of selected surface markers, signaling pathways and omics profiles hampering the identification of myeloid-derived suppressor cells.

    Lutz, Manfred B / Eckert, Ina N

    Cellular immunology

    2021  Band 364, Seite(n) 104347

    Abstract: Myeloid-derived suppressor cells (MDSC) are important immune-regulatory cells but their identification remains difficult. Here, we provide a critical view on selected surface markers, transcriptional and translational pathways commonly used to identify ... ...

    Abstract Myeloid-derived suppressor cells (MDSC) are important immune-regulatory cells but their identification remains difficult. Here, we provide a critical view on selected surface markers, transcriptional and translational pathways commonly used to identify MDSC by specific, their developmental origin and new possibilities by transcriptional or proteomic profiling. Discrimination of MDSC from their non-suppressive counterparts is a prerequisite for the development of successful therapies. Understanding the switch mechanisms that direct granulocytic and monocytic development into a pro-inflammatory or anti-inflammatory direction will be crucial for therapeutic strategies. Manipulation of these myeloid checkpoints are exploited by tumors and pathogens, such as M. tuberculosis (Mtb), HIV or SARS-CoV-2, that induce MDSC for immune evasion. Thus, specific markers for MDSC identification may reveal also novel molecular candidates for therapeutic intervention at the level of MDSC.
    Mesh-Begriff(e) Animals ; B7-H1 Antigen/genetics ; B7-H1 Antigen/immunology ; B7-H1 Antigen/metabolism ; Biomarkers/metabolism ; COVID-19/immunology ; COVID-19/prevention & control ; COVID-19/virology ; Cells, Cultured ; Gene Expression Profiling/methods ; Humans ; Mice ; Myeloid-Derived Suppressor Cells/immunology ; Myeloid-Derived Suppressor Cells/metabolism ; Neoplasms/genetics ; Neoplasms/immunology ; Neoplasms/metabolism ; Programmed Cell Death 1 Receptor/genetics ; Programmed Cell Death 1 Receptor/immunology ; Programmed Cell Death 1 Receptor/metabolism ; Proteomics/methods ; SARS-CoV-2/immunology ; SARS-CoV-2/isolation & purification ; SARS-CoV-2/physiology ; Signal Transduction/genetics ; Signal Transduction/immunology ; T-Lymphocytes, Regulatory/immunology ; T-Lymphocytes, Regulatory/metabolism
    Chemische Substanzen B7-H1 Antigen ; Biomarkers ; Programmed Cell Death 1 Receptor
    Sprache Englisch
    Erscheinungsdatum 2021-03-29
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80094-6
    ISSN 1090-2163 ; 0008-8749
    ISSN (online) 1090-2163
    ISSN 0008-8749
    DOI 10.1016/j.cellimm.2021.104347
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Buch ; Überordnung: Handbook of dendritic cells

    Lutz, Manfred B.

    biology, diseases and therapies

    2006  

    Verfasserangabe ed. by Manfred B.Lutz
    Sprache Englisch
    Erscheinungsverlauf 2006-9999
    Verlag Wiley-VCH
    Erscheinungsort Weinheim
    Erscheinungsland Deutschland
    Dokumenttyp Buch ; Überordnung (Einzelbände anzeigen)
    HBZ-ID HT014563806
    ISBN 978-3-527-31109-5 ; 3-527-31109-2
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  4. Buch: Handbook of dendritic cells / 2

    Lutz, Manfred B.

    biology, diseases and therapies

    2006  

    Verfasserangabe ed. by Manfred B.Lutz
    Überordnung Handbook of dendritic cells
    Sprache Englisch
    Umfang LXXII, S. 385 - 771 : Ill.
    Verlag Wiley-VCH
    Erscheinungsort Weinheim
    Erscheinungsland Deutschland
    Dokumenttyp Buch
    HBZ-ID HT014651216
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  5. Buch: Handbook of dendritic cells / 3

    Lutz, Manfred B.

    biology, diseases and therapies

    2006  

    Verfasserangabe ed. by Manfred B.Lutz
    Überordnung Handbook of dendritic cells
    Sprache Englisch
    Umfang LXVI, S. 773 - 1226 : Ill., graph. Darst.
    Verlag Wiley-VCH
    Erscheinungsort Weinheim
    Erscheinungsland Deutschland
    Dokumenttyp Buch
    HBZ-ID HT014651218
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  6. Buch: Handbook of dendritic cells / 1

    Lutz, Manfred B.

    biology, diseases and therapies

    2006  

    Verfasserangabe ed. by Manfred B.Lutz
    Überordnung Handbook of dendritic cells
    Sprache Englisch
    Umfang LXXIII, 383 S. : Ill., graph. Darst.
    Verlag Wiley-VCH
    Erscheinungsort Weinheim
    Erscheinungsland Deutschland
    Dokumenttyp Buch
    HBZ-ID HT014651212
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  7. Artikel ; Online: M-MDSC

    Aintablian, Arpa / Strozniak, Sandra / Heuer, Marion / Lutz, Manfred B

    Frontiers in immunology

    2023  Band 14, Seite(n) 1130600

    Abstract: Myeloid-derived suppressor cells (MDSC) represent major regulators of immune responses, which can control T ... ...

    Abstract Myeloid-derived suppressor cells (MDSC) represent major regulators of immune responses, which can control T cells
    Mesh-Begriff(e) Mice ; Animals ; Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology ; Myeloid-Derived Suppressor Cells ; Interleukin-3/pharmacology ; Arginase/metabolism ; Bone Marrow/metabolism ; Integrin alpha1
    Chemische Substanzen Granulocyte-Macrophage Colony-Stimulating Factor (83869-56-1) ; Interleukin-3 ; Arginase (EC 3.5.3.1) ; Integrin alpha1
    Sprache Englisch
    Erscheinungsdatum 2023-05-19
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1130600
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Fully functional monocytic MDSC generation from the murine HoxB8 cell line.

    Alattar, Haisam / Xu, Huaming / Zenke, Martin / Lutz, Manfred B

    European journal of immunology

    2023  Band 53, Heft 9, Seite(n) e2350466

    Abstract: Myeloid-derived suppressor cells (MDSC) play a crucial role in controlling T-cell responses, but their development and suppressor mechanisms are not fully understood. To study the molecular functions of MDSC, a large number of standardized cells are ... ...

    Abstract Myeloid-derived suppressor cells (MDSC) play a crucial role in controlling T-cell responses, but their development and suppressor mechanisms are not fully understood. To study the molecular functions of MDSC, a large number of standardized cells are required. Traditionally, bone marrow (BM) has been used to generate myeloid cell types, including MDSC. In this study, we demonstrate that a previously described protocol for generating monocytic MDSC (M-MDSC) from murine BM with GM-CSF can be fully transferred to BM cells that are conditionally transformed with HoxB8 gene (HoxB8 cells). HoxB8 cells have an extended lifespan and efficiently differentiate into MDSC that are quantitatively and qualitatively comparable to M-MDSC from BM cells. Flow cytometric analyses of LPS/IFN-γ activated cultures revealed the same iNOS
    Mesh-Begriff(e) Animals ; Mice ; Myeloid-Derived Suppressor Cells ; Granulocyte-Macrophage Colony-Stimulating Factor/metabolism ; Cell Line ; Myeloid Cells/metabolism ; CD8-Positive T-Lymphocytes
    Chemische Substanzen Granulocyte-Macrophage Colony-Stimulating Factor (83869-56-1)
    Sprache Englisch
    Erscheinungsdatum 2023-06-27
    Erscheinungsland Germany
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120108-6
    ISSN 1521-4141 ; 0014-2980
    ISSN (online) 1521-4141
    ISSN 0014-2980
    DOI 10.1002/eji.202350466
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Induction of CD4(+) Regulatory and Polarized Effector/helper T Cells by Dendritic Cells.

    Lutz, Manfred B

    Immune network

    2016  Band 16, Heft 1, Seite(n) 13–25

    Abstract: Dendritic cells (DCs) are considered to play major roles during the induction of T cell immune responses as well as the maintenance of T cell tolerance. Naive CD4(+) T cells have been shown to respond with high plasticity to signals inducing their ... ...

    Abstract Dendritic cells (DCs) are considered to play major roles during the induction of T cell immune responses as well as the maintenance of T cell tolerance. Naive CD4(+) T cells have been shown to respond with high plasticity to signals inducing their polarization into effector/helper or regulatory T cells. Data obtained from in vitro generated bone-marrow (BM)-derived DCs as well as genetic mouse models revealed an important but not exclusive role of DCs in shaping CD4(+) T cell responses. Besides the specialization of some conventional DC subsets for the induction of polarized immunity, also the maturation stage, activation of specialized transcription factors and the cytokine production of DCs have major impact on CD4(+) T cells. Since in vitro generated BM-DCs show a high diversity to shape CD4(+) T cells and their high similarity to monocyte-derived DCs in vivo, this review reports data mainly on BM-DCs in this process and only touches the roles of transcription factors or of DC subsets, which have been discussed elsewhere. Here, recent findings on 1) the conversion of naive into anergic and further into Foxp3(-) regulatory T cells (Treg) by immature DCs, 2) the role of RelB in steady state migratory DCs (ssmDCs) for conversion of naive T cells into Foxp3(+) Treg, 3) the DC maturation signature for polarized Th2 cell induction and 4) the DC source of IL-12 for Th1 induction are discussed.
    Sprache Englisch
    Erscheinungsdatum 2016-02-25
    Erscheinungsland Korea (South)
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2536191-0
    ISSN 2092-6685 ; 1598-2629
    ISSN (online) 2092-6685
    ISSN 1598-2629
    DOI 10.4110/in.2016.16.1.13
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Revisiting Current Concepts on the Tolerogenicity of Steady-State Dendritic Cell Subsets and Their Maturation Stages.

    Lutz, Manfred B / Backer, Ronald A / Clausen, Björn E

    Journal of immunology (Baltimore, Md. : 1950)

    2021  Band 206, Heft 8, Seite(n) 1681–1689

    Abstract: The original concept stated that immature dendritic cells (DC) act tolerogenically whereas mature DC behave strictly immunogenically. Meanwhile, it is also accepted that phenotypically mature stages of all conventional DC subsets can promote tolerance as ...

    Abstract The original concept stated that immature dendritic cells (DC) act tolerogenically whereas mature DC behave strictly immunogenically. Meanwhile, it is also accepted that phenotypically mature stages of all conventional DC subsets can promote tolerance as steady-state migratory DC by transporting self-antigens to lymph nodes to exert unique functions on regulatory T cells. We propose that in vivo 1) there is little evidence for a tolerogenic function of immature DC during steady state such as CD4 T cell anergy induction, 2) all tolerance as steady-state migratory DC undergo common as well as subset-specific molecular changes, and 3) these changes differ by quantitative and qualitative markers from immunogenic DC, which allows one to clearly distinguish tolerogenic from immunogenic migratory DC.
    Mesh-Begriff(e) Animals ; Autoimmunity ; Cell Differentiation ; Cell Movement ; Dendritic Cells/immunology ; Humans ; Immune Tolerance/immunology ; Immunity, Cellular ; Models, Immunological ; T-Lymphocytes, Regulatory/immunology
    Sprache Englisch
    Erscheinungsdatum 2021-06-16
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Review
    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.2001315
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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