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  1. Article ; Online: CD28 and IL-4: two heavyweights controlling the balance between immunity and inflammation.

    Hünig, Thomas / Lühder, Fred / Elflein, Karin / Gogishvili, Tea / Fröhlich, Monika / Guler, Reto / Cutler, Antony / Brombacher, Frank

    Medical microbiology and immunology

    2010  Volume 199, Issue 3, Page(s) 239–246

    Abstract: ... immune modulation by CD28 and IL-4 is interconnected through the promotion of IL-4 producing T-helper 2 cells ... in controlling the size and quality of pathogen-specific immune responses. Thus, CD28-mediated costimulation is ... The costimulatory receptor CD28 and IL-4Ralpha containing cytokine receptors play key roles ...

    Abstract The costimulatory receptor CD28 and IL-4Ralpha containing cytokine receptors play key roles in controlling the size and quality of pathogen-specific immune responses. Thus, CD28-mediated costimulation is needed for effective primary T-cell expansion and for the generation and activation of regulatory T-cells (Treg cells), which protect from immunopathology. Similarly, IL-4Ralpha signals are required for alternative activation of macrophages, which counteract inflammation by type 1 responses. Furthermore,immune modulation by CD28 and IL-4 is interconnected through the promotion of IL-4 producing T-helper 2 cells by CD28 signals. Using conditionally IL-4Ralpha and CD28 deleting mice, as well as monoclonal antibodies, which block or stimulate CD28, or mAb that deplete Treg cells, we have studied the roles of CD28 and IL-4Ralpha in experimental mouse models of virus (influenza), intracellular bacteria (L. monocytogenes, M. tuberculosis), and parasite infections (T. congolense, L. major). We observed that in some, but not all settings, Treg cells and type 2 immune deviation, including activation of alternative macrophages can be manipulated to protect the host either from infection or from immunopathology with an overall beneficial outcome. Furthermore, we provide direct evidence that secondary CD8 T-cell responses to i.c. bacteria are dependent on CD28-mediated costimulation.
    MeSH term(s) Animals ; CD28 Antigens/immunology ; Disease Models, Animal ; Immunity ; Inflammation ; Interleukin-4/immunology ; Leishmaniasis, Cutaneous/immunology ; Leishmaniasis, Cutaneous/pathology ; Listeriosis/immunology ; Listeriosis/pathology ; Macrophages/immunology ; Mice ; Orthomyxoviridae Infections/immunology ; Orthomyxoviridae Infections/pathology ; T-Lymphocytes/immunology ; Trypanosomiasis, African/immunology ; Trypanosomiasis, African/pathology ; Tuberculosis/immunology ; Tuberculosis/pathology
    Chemical Substances CD28 Antigens ; Interleukin-4 (207137-56-2)
    Language English
    Publishing date 2010-04-14
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 120933-4
    ISSN 1432-1831 ; 0300-8584
    ISSN (online) 1432-1831
    ISSN 0300-8584
    DOI 10.1007/s00430-010-0156-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: CD28 and IL-4: two heavyweights controlling the balance between immunity and inflammation

    Hünig, Thomas / Lühder, Fred / Elflein, Karin / Gogishvili, Tea / Fröhlich, Monika / Guler, Reto / Cutler, Antony / Brombacher, Frank

    Medical microbiology and immunology. 2010 Aug., v. 199, no. 3

    2010  

    Abstract: ... activation of macrophages, which counteract inflammation by type 1 responses. Furthermore, immune modulation by CD28 and IL ... in controlling the size and quality of pathogen-specific immune responses. Thus, CD28-mediated costimulation is ... The costimulatory receptor CD28 and IL-4Rα-containing cytokine receptors play key roles ...

    Abstract The costimulatory receptor CD28 and IL-4Rα-containing cytokine receptors play key roles in controlling the size and quality of pathogen-specific immune responses. Thus, CD28-mediated costimulation is needed for effective primary T-cell expansion and for the generation and activation of regulatory T-cells (Treg cells), which protect from immunopathology. Similarly, IL-4Rα signals are required for alternative activation of macrophages, which counteract inflammation by type 1 responses. Furthermore, immune modulation by CD28 and IL-4 is interconnected through the promotion of IL-4 producing T-helper 2 cells by CD28 signals. Using conditionally IL-4Rα and CD28 deleting mice, as well as monoclonal antibodies, which block or stimulate CD28, or mAb that deplete Treg cells, we have studied the roles of CD28 and IL-4Rα in experimental mouse models of virus (influenza), intracellular bacteria (L. monocytogenes, M. tuberculosis), and parasite infections (T. congolense, L. major). We observed that in some, but not all settings, Treg cells and type 2 immune deviation, including activation of alternative macrophages can be manipulated to protect the host either from infection or from immunopathology with an overall beneficial outcome. Furthermore, we provide direct evidence that secondary CD8 T-cell responses to i.c. bacteria are dependent on CD28-mediated costimulation.
    Keywords monoclonal antibodies ; influenza
    Language English
    Dates of publication 2010-08
    Size p. 239-246.
    Publisher Springer-Verlag
    Publishing place Berlin/Heidelberg
    Document type Article
    ZDB-ID 120933-4
    ISSN 1432-1831 ; 0300-8584
    ISSN (online) 1432-1831
    ISSN 0300-8584
    DOI 10.1007/s00430-010-0156-z
    Database NAL-Catalogue (AGRICOLA)

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