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      Recombinant porcine interferon-gamma activates in vitro porcine adherent mononuclear cells to produce interleukin 1

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      Veterinary Immunology and Immunopathology
      Published by Elsevier B.V.

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          Abstract

          The effect of recombinant porcine interferon-gamma (rPoIFNγ) on in vitro production of interleukin 1 (IL-1) by porcine blood monocytes was studied. Three-day-old cultures of porcine adherent blood mononuclear cells were treated by doses of rPoIFNγ for 3 or 6 days before lipopolysaccharide (LPS)-induction. While rPoIFNγ alone had no effect, a combined treatment by rPoIFNγ and LPS enhanced the IL-1 secretory potential of adherent mononuclear cells and, to a lesser extent, the level of cell-associated IL-1. The IL-1 activity was neutralized by anti porcine IL-1 α and β antisera. These results demonstrate that rPoIFNγ has immunomodulatory effects in vitro on porcine monokine production.

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          Most cited references16

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          Immune interferon: a pleiotropic lymphokine with multiple effects.

          Immune (gamma) interferon (IFN-γ) is produced during an immune response by antigen-specific T cells and probably also by natural killer (NK) cells recruited by the T cell-product interleukin 2 (IL-2). IFN-γ was discovered and originally measured on the basis of its anti-viral activity, but its complex anti-cellular activities probably reflect its biological role more clearly. In this review, Giorgio Trinchieri and Bice Perussia discuss some aspects of the biology of IFN-γ, its pleiomorphic anti-cellular effects and its ability to modulate cellular responses to other regulatory factors.
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            Effect of interferon-alpha, interferon-gamma and tumour necrosis factor on African swine fever virus replication in porcine monocytes and macrophages.

            Bovine interferon-alpha I1 (IFN-alpha I1) and porcine interferon-gamma (IFN-gamma) inhibited African swine fever virus replication in both porcine monocytes and alveolar macrophages. The most potent antiviral activity was observed with IFN-gamma-treated alveolar macrophages. The production of both a virulent (CC83) and a non-virulent (BA71) isolate of the virus was inhibited. Bovine tumour necrosis factor alpha did not show antiviral activity in either monocytes or alveolar macrophages. Rather, an increase of African swine fever virus production in tumour necrosis factor alpha-treated monocytes was found. An analysis of viral protein synthesis in IFN-alpha I1- and IFN-gamma-treated alveolar macrophages showed an inhibition of synthesis of some viral proteins. The inhibition of late proteins was very pronounced in IFN-gamma-treated cells, and it was probably a consequence of the inhibition of African swine fever virus DNA polymerase activity.
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              A newly defined property of somatotropin: priming of macrophages for production of superoxide anion

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                Author and article information

                Journal
                Vet Immunol Immunopathol
                Vet. Immunol. Immunopathol
                Veterinary Immunology and Immunopathology
                Published by Elsevier B.V.
                0165-2427
                1873-2534
                12 November 2002
                June 1990
                12 November 2002
                : 25
                : 2
                : 117-124
                Affiliations
                INRA, Station de Virologie et d'Immunologie Moléculaires, 78350 Jouy-en-Josas France
                Article
                0165-2427(90)90029-R
                10.1016/0165-2427(90)90029-R
                7119577
                2116051
                b91dabf9-4a01-4564-92a4-1c40b1de7f26
                Copyright © 1990 Published by Elsevier B.V.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 23 November 1989
                Categories
                Article

                Veterinary medicine
                Veterinary medicine

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