OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.

OX40, a member of the TNF receptor superfamily, is expressed on activated T cells and implicated in stimulation of T cells and T-dependent humoral responses. We generated OX40-/- mice and found that the formation of extrafollicular plasma cells, germinal centers, and antibody responses was independe...

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Main Authors: Kopf, M, Ruedl, C, Schmitz, N, Gallimore, A, Lefrang, K, Ecabert, B, Odermatt, B, Bachmann, M
Format: Journal article
Language:English
Published: 1999
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author Kopf, M
Ruedl, C
Schmitz, N
Gallimore, A
Lefrang, K
Ecabert, B
Odermatt, B
Bachmann, M
author_facet Kopf, M
Ruedl, C
Schmitz, N
Gallimore, A
Lefrang, K
Ecabert, B
Odermatt, B
Bachmann, M
author_sort Kopf, M
collection OXFORD
description OX40, a member of the TNF receptor superfamily, is expressed on activated T cells and implicated in stimulation of T cells and T-dependent humoral responses. We generated OX40-/- mice and found that the formation of extrafollicular plasma cells, germinal centers, and antibody responses was independent of OX40. After infection with LCMV and influenza virus, OX40-/- mice retain primary and memory cytotoxic T cell responses with normal expansion and decline of specific CTL. In contrast, CD4+ T cell proliferation and the number of IFN-gamma-producing CD4+ T cells were reduced in OX40-/- mice. Moreover, the number of CD4+ T cells infiltrating the lungs of influenza virus-infected OX40-/- mice was reduced. These results define a unique role of OX40 in the generation of optimal CD4+ T cell responses in vivo.
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spelling oxford-uuid:c0dd1237-7e7d-4aa2-bbd8-8b9e3e6005c92022-03-27T05:57:24ZOX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c0dd1237-7e7d-4aa2-bbd8-8b9e3e6005c9EnglishSymplectic Elements at Oxford1999Kopf, MRuedl, CSchmitz, NGallimore, ALefrang, KEcabert, BOdermatt, BBachmann, MOX40, a member of the TNF receptor superfamily, is expressed on activated T cells and implicated in stimulation of T cells and T-dependent humoral responses. We generated OX40-/- mice and found that the formation of extrafollicular plasma cells, germinal centers, and antibody responses was independent of OX40. After infection with LCMV and influenza virus, OX40-/- mice retain primary and memory cytotoxic T cell responses with normal expansion and decline of specific CTL. In contrast, CD4+ T cell proliferation and the number of IFN-gamma-producing CD4+ T cells were reduced in OX40-/- mice. Moreover, the number of CD4+ T cells infiltrating the lungs of influenza virus-infected OX40-/- mice was reduced. These results define a unique role of OX40 in the generation of optimal CD4+ T cell responses in vivo.
spellingShingle Kopf, M
Ruedl, C
Schmitz, N
Gallimore, A
Lefrang, K
Ecabert, B
Odermatt, B
Bachmann, M
OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title_full OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title_fullStr OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title_full_unstemmed OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title_short OX40-deficient mice are defective in Th cell proliferation but are competent in generating B cell and CTL Responses after virus infection.
title_sort ox40 deficient mice are defective in th cell proliferation but are competent in generating b cell and ctl responses after virus infection
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