Osteopontin is not required for the development of Th1 responses and viral immunity.

Osteopontin (OPN) has been defined as a key cytokine promoting the release of IL-12 and hence inducing the development of protective cell-mediated immunity to viruses and intracellular pathogens. To further characterize the role of OPN in antiviral immunity, OPN-deficient (OPN-/-) mice were analyzed...

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Päätekijät: Abel, B, Freigang, S, Bachmann, M, Boschert, U, Kopf, M
Aineistotyyppi: Journal article
Kieli:English
Julkaistu: 2005
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author Abel, B
Freigang, S
Bachmann, M
Boschert, U
Kopf, M
author_facet Abel, B
Freigang, S
Bachmann, M
Boschert, U
Kopf, M
author_sort Abel, B
collection OXFORD
description Osteopontin (OPN) has been defined as a key cytokine promoting the release of IL-12 and hence inducing the development of protective cell-mediated immunity to viruses and intracellular pathogens. To further characterize the role of OPN in antiviral immunity, OPN-deficient (OPN-/-) mice were analyzed after infection with influenza virus and vaccinia virus. Surprisingly, we found that viral clearance, lung inflammation, and recruitment of effector T cells to the lung were unaffected in OPN-/- mice after influenza infection. Furthermore, effector status of T cells was normal as demonstrated by normal IFN-gamma production and CTL lytic activity. Moreover, activation and Th1 differentiation of naive TCR transgenic CD4+ T cells by dendritic cells and cognate Ag was normal in the absence of OPN in vitro. Contrary to a previous report, we found that OPN-/- mice mounted a normal immune response to Listeria monocytogenes. In conclusion, OPN is dispensable for antiviral immune responses against influenza virus and vaccinia virus.
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spelling oxford-uuid:a3dae49e-2ed2-4448-a10a-01243d51e3f32022-03-27T02:29:58ZOsteopontin is not required for the development of Th1 responses and viral immunity.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a3dae49e-2ed2-4448-a10a-01243d51e3f3EnglishSymplectic Elements at Oxford2005Abel, BFreigang, SBachmann, MBoschert, UKopf, MOsteopontin (OPN) has been defined as a key cytokine promoting the release of IL-12 and hence inducing the development of protective cell-mediated immunity to viruses and intracellular pathogens. To further characterize the role of OPN in antiviral immunity, OPN-deficient (OPN-/-) mice were analyzed after infection with influenza virus and vaccinia virus. Surprisingly, we found that viral clearance, lung inflammation, and recruitment of effector T cells to the lung were unaffected in OPN-/- mice after influenza infection. Furthermore, effector status of T cells was normal as demonstrated by normal IFN-gamma production and CTL lytic activity. Moreover, activation and Th1 differentiation of naive TCR transgenic CD4+ T cells by dendritic cells and cognate Ag was normal in the absence of OPN in vitro. Contrary to a previous report, we found that OPN-/- mice mounted a normal immune response to Listeria monocytogenes. In conclusion, OPN is dispensable for antiviral immune responses against influenza virus and vaccinia virus.
spellingShingle Abel, B
Freigang, S
Bachmann, M
Boschert, U
Kopf, M
Osteopontin is not required for the development of Th1 responses and viral immunity.
title Osteopontin is not required for the development of Th1 responses and viral immunity.
title_full Osteopontin is not required for the development of Th1 responses and viral immunity.
title_fullStr Osteopontin is not required for the development of Th1 responses and viral immunity.
title_full_unstemmed Osteopontin is not required for the development of Th1 responses and viral immunity.
title_short Osteopontin is not required for the development of Th1 responses and viral immunity.
title_sort osteopontin is not required for the development of th1 responses and viral immunity
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AT freigangs osteopontinisnotrequiredforthedevelopmentofth1responsesandviralimmunity
AT bachmannm osteopontinisnotrequiredforthedevelopmentofth1responsesandviralimmunity
AT boschertu osteopontinisnotrequiredforthedevelopmentofth1responsesandviralimmunity
AT kopfm osteopontinisnotrequiredforthedevelopmentofth1responsesandviralimmunity