Interleukin-12
Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, pro...
Ausführliche Beschreibung
Autor*in: |
Trinchieri, Giorgio [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
1995 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: BioDrugs - Berlin [u.a.] : Springer, 1997, 3(1995), 4 vom: Apr., Seite 262-270 |
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Übergeordnetes Werk: |
volume:3 ; year:1995 ; number:4 ; month:04 ; pages:262-270 |
Links: |
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DOI / URN: |
10.1007/BF03259278 |
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Katalog-ID: |
SPR032977735 |
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520 | |a Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. | ||
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10.1007/BF03259278 doi (DE-627)SPR032977735 (SPR)BF03259278-e DE-627 ger DE-627 rakwb eng 610 ASE Trinchieri, Giorgio verfasserin aut Interleukin-12 1995 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. Adis International Limited (dpeaa)DE-He213 Cutaneous Leishmaniasis (dpeaa)DE-He213 Heterodimeric Cytokine (dpeaa)DE-He213 Shwartzman Reaction (dpeaa)DE-He213 Natural Killer Cell Stimulatory Factor (dpeaa)DE-He213 Enthalten in BioDrugs Berlin [u.a.] : Springer, 1997 3(1995), 4 vom: Apr., Seite 262-270 (DE-627)327644672 (DE-600)2043743-2 1179-190X nnns volume:3 year:1995 number:4 month:04 pages:262-270 https://dx.doi.org/10.1007/BF03259278 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE AR 3 1995 4 04 262-270 |
spelling |
10.1007/BF03259278 doi (DE-627)SPR032977735 (SPR)BF03259278-e DE-627 ger DE-627 rakwb eng 610 ASE Trinchieri, Giorgio verfasserin aut Interleukin-12 1995 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. Adis International Limited (dpeaa)DE-He213 Cutaneous Leishmaniasis (dpeaa)DE-He213 Heterodimeric Cytokine (dpeaa)DE-He213 Shwartzman Reaction (dpeaa)DE-He213 Natural Killer Cell Stimulatory Factor (dpeaa)DE-He213 Enthalten in BioDrugs Berlin [u.a.] : Springer, 1997 3(1995), 4 vom: Apr., Seite 262-270 (DE-627)327644672 (DE-600)2043743-2 1179-190X nnns volume:3 year:1995 number:4 month:04 pages:262-270 https://dx.doi.org/10.1007/BF03259278 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE AR 3 1995 4 04 262-270 |
allfields_unstemmed |
10.1007/BF03259278 doi (DE-627)SPR032977735 (SPR)BF03259278-e DE-627 ger DE-627 rakwb eng 610 ASE Trinchieri, Giorgio verfasserin aut Interleukin-12 1995 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. Adis International Limited (dpeaa)DE-He213 Cutaneous Leishmaniasis (dpeaa)DE-He213 Heterodimeric Cytokine (dpeaa)DE-He213 Shwartzman Reaction (dpeaa)DE-He213 Natural Killer Cell Stimulatory Factor (dpeaa)DE-He213 Enthalten in BioDrugs Berlin [u.a.] : Springer, 1997 3(1995), 4 vom: Apr., Seite 262-270 (DE-627)327644672 (DE-600)2043743-2 1179-190X nnns volume:3 year:1995 number:4 month:04 pages:262-270 https://dx.doi.org/10.1007/BF03259278 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE AR 3 1995 4 04 262-270 |
allfieldsGer |
10.1007/BF03259278 doi (DE-627)SPR032977735 (SPR)BF03259278-e DE-627 ger DE-627 rakwb eng 610 ASE Trinchieri, Giorgio verfasserin aut Interleukin-12 1995 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. Adis International Limited (dpeaa)DE-He213 Cutaneous Leishmaniasis (dpeaa)DE-He213 Heterodimeric Cytokine (dpeaa)DE-He213 Shwartzman Reaction (dpeaa)DE-He213 Natural Killer Cell Stimulatory Factor (dpeaa)DE-He213 Enthalten in BioDrugs Berlin [u.a.] : Springer, 1997 3(1995), 4 vom: Apr., Seite 262-270 (DE-627)327644672 (DE-600)2043743-2 1179-190X nnns volume:3 year:1995 number:4 month:04 pages:262-270 https://dx.doi.org/10.1007/BF03259278 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE AR 3 1995 4 04 262-270 |
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10.1007/BF03259278 doi (DE-627)SPR032977735 (SPR)BF03259278-e DE-627 ger DE-627 rakwb eng 610 ASE Trinchieri, Giorgio verfasserin aut Interleukin-12 1995 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. Adis International Limited (dpeaa)DE-He213 Cutaneous Leishmaniasis (dpeaa)DE-He213 Heterodimeric Cytokine (dpeaa)DE-He213 Shwartzman Reaction (dpeaa)DE-He213 Natural Killer Cell Stimulatory Factor (dpeaa)DE-He213 Enthalten in BioDrugs Berlin [u.a.] : Springer, 1997 3(1995), 4 vom: Apr., Seite 262-270 (DE-627)327644672 (DE-600)2043743-2 1179-190X nnns volume:3 year:1995 number:4 month:04 pages:262-270 https://dx.doi.org/10.1007/BF03259278 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE AR 3 1995 4 04 262-270 |
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Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. |
abstractGer |
Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. |
abstract_unstemmed |
Summary Interleukin (IL)-12 is a heterodimeric cytokine produced by phagocytic cells, T cells and other antigen-presenting cells, mostly in response to bacteria, bacterial products and intracellular parasites. IL-12 is active on T cells and natural killer cells, inducing production of cytokines, proliferation and enhancement of cytotoxic activity. Early during infections, IL-12 production induces interferon-γ (IFNγ), which in turn activates phagocytic cells and enhances their bacteriological activity. IL-12 and IFNγ also direct the development of T helper type 1 ($ T_{H} $1) cells, which produce interleukin-2 and IFNγ and activate cell-mediated resistance mechanisms against many pathogens. In several experimental models of infection, treatment with recombinant IL-12 has been shown to increase the immune resistance against infection. IL-12 is also an effective adjuvant in vaccines, favouring the development of protective $ T_{H} $1 memory responses. The ability of IL-12 to enhance the cellular immune response also makes it an effective agent for boosting the immune resistance against tumours. Thus, IL-12 has clinical potential as a therapeutic agent in infectious diseases and cancer. The immunopotentiating activity of IL-12, and the fact that cells from HIV-positive patients have a decreased ability to produce this cytokine, suggest the possible clinical use of IL-12 in AIDS therapy. |
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title_short |
Interleukin-12 |
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10.1007/BF03259278 |
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