author_facet Hoyer, Katrina K.
Kuswanto, Wilson F.
Gallo, Eugenio
Abbas, Abul K.
Hoyer, Katrina K.
Kuswanto, Wilson F.
Gallo, Eugenio
Abbas, Abul K.
author Hoyer, Katrina K.
Kuswanto, Wilson F.
Gallo, Eugenio
Abbas, Abul K.
spellingShingle Hoyer, Katrina K.
Kuswanto, Wilson F.
Gallo, Eugenio
Abbas, Abul K.
Blood
Distinct roles of helper T-cell subsets in a systemic autoimmune disease
Cell Biology
Hematology
Immunology
Biochemistry
author_sort hoyer, katrina k.
spelling Hoyer, Katrina K. Kuswanto, Wilson F. Gallo, Eugenio Abbas, Abul K. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2008-04-153346 <jats:title>Abstract</jats:title><jats:p>Imbalance of T-helper cell (Th) differentiation and subsequent cytokine dysregulation is implicated in inflammatory and autoimmune diseases. In particular, 2 cytokines produced by different Th cell populations, interferon-γ (IFN-γ) and interleukin-17 (IL-17), have been shown to play a critical role in autoimmunity. We have examined the roles of these cytokines in a mouse model of systemic autoimmunity resulting from the deletion of IL-2 in which autoimmune hemolytic anemia (AIHA) is a prominent feature. We demonstrate that, in IL-2–knockout (KO) BALB/c mice, elimination of the Th1 cytokine, IFN-γ, delays the development of AIHA. Further, CD4+ T cells from IL-2/IFN-γ–KO mice produce elevated levels of IL-17 compared with wild-type (WT) and IL-2–KO, and these mice eventually develop intestinal inflammation. In contrast, elimination of the Th17 cytokine, IL-17, from IL-2–KO mice fails to suppress early acute AIHA development. These results suggest that in a systemic autoimmune disease with multiple manifestations, Th1 cells drive the early autoantibody response and IL-17–producing cells may be responsible for the more chronic tissue inflammation.</jats:p> Distinct roles of helper T-cell subsets in a systemic autoimmune disease Blood
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source_id 49
title Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_unstemmed Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_full Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_fullStr Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_full_unstemmed Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_short Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_sort distinct roles of helper t-cell subsets in a systemic autoimmune disease
topic Cell Biology
Hematology
Immunology
Biochemistry
url http://dx.doi.org/10.1182/blood-2008-04-153346
publishDate 2009
physical 389-395
description <jats:title>Abstract</jats:title><jats:p>Imbalance of T-helper cell (Th) differentiation and subsequent cytokine dysregulation is implicated in inflammatory and autoimmune diseases. In particular, 2 cytokines produced by different Th cell populations, interferon-γ (IFN-γ) and interleukin-17 (IL-17), have been shown to play a critical role in autoimmunity. We have examined the roles of these cytokines in a mouse model of systemic autoimmunity resulting from the deletion of IL-2 in which autoimmune hemolytic anemia (AIHA) is a prominent feature. We demonstrate that, in IL-2–knockout (KO) BALB/c mice, elimination of the Th1 cytokine, IFN-γ, delays the development of AIHA. Further, CD4+ T cells from IL-2/IFN-γ–KO mice produce elevated levels of IL-17 compared with wild-type (WT) and IL-2–KO, and these mice eventually develop intestinal inflammation. In contrast, elimination of the Th17 cytokine, IL-17, from IL-2–KO mice fails to suppress early acute AIHA development. These results suggest that in a systemic autoimmune disease with multiple manifestations, Th1 cells drive the early autoantibody response and IL-17–producing cells may be responsible for the more chronic tissue inflammation.</jats:p>
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author Hoyer, Katrina K., Kuswanto, Wilson F., Gallo, Eugenio, Abbas, Abul K.
author_facet Hoyer, Katrina K., Kuswanto, Wilson F., Gallo, Eugenio, Abbas, Abul K., Hoyer, Katrina K., Kuswanto, Wilson F., Gallo, Eugenio, Abbas, Abul K.
author_sort hoyer, katrina k.
container_issue 2
container_start_page 389
container_title Blood
container_volume 113
description <jats:title>Abstract</jats:title><jats:p>Imbalance of T-helper cell (Th) differentiation and subsequent cytokine dysregulation is implicated in inflammatory and autoimmune diseases. In particular, 2 cytokines produced by different Th cell populations, interferon-γ (IFN-γ) and interleukin-17 (IL-17), have been shown to play a critical role in autoimmunity. We have examined the roles of these cytokines in a mouse model of systemic autoimmunity resulting from the deletion of IL-2 in which autoimmune hemolytic anemia (AIHA) is a prominent feature. We demonstrate that, in IL-2–knockout (KO) BALB/c mice, elimination of the Th1 cytokine, IFN-γ, delays the development of AIHA. Further, CD4+ T cells from IL-2/IFN-γ–KO mice produce elevated levels of IL-17 compared with wild-type (WT) and IL-2–KO, and these mice eventually develop intestinal inflammation. In contrast, elimination of the Th17 cytokine, IL-17, from IL-2–KO mice fails to suppress early acute AIHA development. These results suggest that in a systemic autoimmune disease with multiple manifestations, Th1 cells drive the early autoantibody response and IL-17–producing cells may be responsible for the more chronic tissue inflammation.</jats:p>
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spelling Hoyer, Katrina K. Kuswanto, Wilson F. Gallo, Eugenio Abbas, Abul K. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2008-04-153346 <jats:title>Abstract</jats:title><jats:p>Imbalance of T-helper cell (Th) differentiation and subsequent cytokine dysregulation is implicated in inflammatory and autoimmune diseases. In particular, 2 cytokines produced by different Th cell populations, interferon-γ (IFN-γ) and interleukin-17 (IL-17), have been shown to play a critical role in autoimmunity. We have examined the roles of these cytokines in a mouse model of systemic autoimmunity resulting from the deletion of IL-2 in which autoimmune hemolytic anemia (AIHA) is a prominent feature. We demonstrate that, in IL-2–knockout (KO) BALB/c mice, elimination of the Th1 cytokine, IFN-γ, delays the development of AIHA. Further, CD4+ T cells from IL-2/IFN-γ–KO mice produce elevated levels of IL-17 compared with wild-type (WT) and IL-2–KO, and these mice eventually develop intestinal inflammation. In contrast, elimination of the Th17 cytokine, IL-17, from IL-2–KO mice fails to suppress early acute AIHA development. These results suggest that in a systemic autoimmune disease with multiple manifestations, Th1 cells drive the early autoantibody response and IL-17–producing cells may be responsible for the more chronic tissue inflammation.</jats:p> Distinct roles of helper T-cell subsets in a systemic autoimmune disease Blood
spellingShingle Hoyer, Katrina K., Kuswanto, Wilson F., Gallo, Eugenio, Abbas, Abul K., Blood, Distinct roles of helper T-cell subsets in a systemic autoimmune disease, Cell Biology, Hematology, Immunology, Biochemistry
title Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_full Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_fullStr Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_full_unstemmed Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_short Distinct roles of helper T-cell subsets in a systemic autoimmune disease
title_sort distinct roles of helper t-cell subsets in a systemic autoimmune disease
title_unstemmed Distinct roles of helper T-cell subsets in a systemic autoimmune disease
topic Cell Biology, Hematology, Immunology, Biochemistry
url http://dx.doi.org/10.1182/blood-2008-04-153346