Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep

In small ruminant lentivirus infections, cellular immune responses are diminished in clinically affected animals. The underlying mechanisms for this are unknown. In this study, we tested the hypothesis that alterations in expression of the co-stimulatory molecules B7-1 and B7-2 are involved in infections with Visna/Maedi virus (VMV), the prototype lentivirus of sheep. We studied B7 expression levels ex vivo in peripheral blood mononuclear cells (PBMCs), determining B7 RNA levels by real time reverse transcriptase polymerase chain reaction in asymptomatic as well as clinically affected VMV-seropositive sheep. The levels of both B7 molecules were increased in VMV-seropositive asymptomatic sheep. However, in VMV clinically affected sheep, the level of CD80 (but not CD86) was low compared with the level in uninfected sheep (p < 0.05). CD80 and CD86 RNA levels were associated with the ability of PBMCs to respond to VMV gag antigens (p14, p17, and p25) by proliferation, with most seropositive asymptomatic sheep showing positive proliferative responses but clinically affected sheep showing no response. The response to p25 in clinically affected animals was increased by the addition of interleukin-2 to the cultures. Decreased recall responses to unrelated antigens (assessed by production of interferon-γ) were also found in clinically affected sheep. Thus, among seropositive sheep, decreased B7-1 (CD80) RNA levels and diminished antigen-specific cellular immune responses in PBMCs point to a VMV disease status, whereas increased CD80 and CD86 levels and augmented cellular responses are linked to asymptomatic infection. © 2007 Mary Ann Liebert, Inc.

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Main Authors: Reina, Ramsés, Glaria, Idoia, Benavides, Julio, Andrés, Ximena de, Crespo, Helena, Solano Goñi, Cristina, Pérez Pérez, Valentín, Luján, Lluís, Pérez, Marta M., Pérez de la Lastra, José María, Rosati, Sergio, Blacklaws, Barbara, Harkiss, Gordon D., Andrés, Damián F. de, Amorena Zabalza, Beatriz
Format: artículo biblioteca
Published: Mary Ann Liebert 2007-12-25
Online Access:http://hdl.handle.net/10261/100092
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spelling dig-igm-es-10261-1000922021-04-13T15:21:04Z Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep Reina, Ramsés Glaria, Idoia Benavides, Julio Andrés, Ximena de Crespo, Helena Solano Goñi, Cristina Pérez Pérez, Valentín Luján, Lluís Pérez, Marta M. Pérez de la Lastra, José María Rosati, Sergio Blacklaws, Barbara Harkiss, Gordon D. Andrés, Damián F. de Amorena Zabalza, Beatriz In small ruminant lentivirus infections, cellular immune responses are diminished in clinically affected animals. The underlying mechanisms for this are unknown. In this study, we tested the hypothesis that alterations in expression of the co-stimulatory molecules B7-1 and B7-2 are involved in infections with Visna/Maedi virus (VMV), the prototype lentivirus of sheep. We studied B7 expression levels ex vivo in peripheral blood mononuclear cells (PBMCs), determining B7 RNA levels by real time reverse transcriptase polymerase chain reaction in asymptomatic as well as clinically affected VMV-seropositive sheep. The levels of both B7 molecules were increased in VMV-seropositive asymptomatic sheep. However, in VMV clinically affected sheep, the level of CD80 (but not CD86) was low compared with the level in uninfected sheep (p < 0.05). CD80 and CD86 RNA levels were associated with the ability of PBMCs to respond to VMV gag antigens (p14, p17, and p25) by proliferation, with most seropositive asymptomatic sheep showing positive proliferative responses but clinically affected sheep showing no response. The response to p25 in clinically affected animals was increased by the addition of interleukin-2 to the cultures. Decreased recall responses to unrelated antigens (assessed by production of interferon-γ) were also found in clinically affected sheep. Thus, among seropositive sheep, decreased B7-1 (CD80) RNA levels and diminished antigen-specific cellular immune responses in PBMCs point to a VMV disease status, whereas increased CD80 and CD86 levels and augmented cellular responses are linked to asymptomatic infection. © 2007 Mary Ann Liebert, Inc. Peer Reviewed 2014-07-17T11:01:43Z 2014-07-17T11:01:43Z 2007-12-25 2014-07-17T11:01:43Z artículo http://purl.org/coar/resource_type/c_6501 Viral Immunology 20(4): 609-622 (2007) 0882-8245 http://hdl.handle.net/10261/100092 10.1089/vim.2007.0071 http://dx.doi.org/10.1089/vim.2007.0071 none Mary Ann Liebert
institution IGM ES
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country España
countrycode ES
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databasecode dig-igm-es
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libraryname Biblioteca del IGM España
description In small ruminant lentivirus infections, cellular immune responses are diminished in clinically affected animals. The underlying mechanisms for this are unknown. In this study, we tested the hypothesis that alterations in expression of the co-stimulatory molecules B7-1 and B7-2 are involved in infections with Visna/Maedi virus (VMV), the prototype lentivirus of sheep. We studied B7 expression levels ex vivo in peripheral blood mononuclear cells (PBMCs), determining B7 RNA levels by real time reverse transcriptase polymerase chain reaction in asymptomatic as well as clinically affected VMV-seropositive sheep. The levels of both B7 molecules were increased in VMV-seropositive asymptomatic sheep. However, in VMV clinically affected sheep, the level of CD80 (but not CD86) was low compared with the level in uninfected sheep (p < 0.05). CD80 and CD86 RNA levels were associated with the ability of PBMCs to respond to VMV gag antigens (p14, p17, and p25) by proliferation, with most seropositive asymptomatic sheep showing positive proliferative responses but clinically affected sheep showing no response. The response to p25 in clinically affected animals was increased by the addition of interleukin-2 to the cultures. Decreased recall responses to unrelated antigens (assessed by production of interferon-γ) were also found in clinically affected sheep. Thus, among seropositive sheep, decreased B7-1 (CD80) RNA levels and diminished antigen-specific cellular immune responses in PBMCs point to a VMV disease status, whereas increased CD80 and CD86 levels and augmented cellular responses are linked to asymptomatic infection. © 2007 Mary Ann Liebert, Inc.
format artículo
author Reina, Ramsés
Glaria, Idoia
Benavides, Julio
Andrés, Ximena de
Crespo, Helena
Solano Goñi, Cristina
Pérez Pérez, Valentín
Luján, Lluís
Pérez, Marta M.
Pérez de la Lastra, José María
Rosati, Sergio
Blacklaws, Barbara
Harkiss, Gordon D.
Andrés, Damián F. de
Amorena Zabalza, Beatriz
spellingShingle Reina, Ramsés
Glaria, Idoia
Benavides, Julio
Andrés, Ximena de
Crespo, Helena
Solano Goñi, Cristina
Pérez Pérez, Valentín
Luján, Lluís
Pérez, Marta M.
Pérez de la Lastra, José María
Rosati, Sergio
Blacklaws, Barbara
Harkiss, Gordon D.
Andrés, Damián F. de
Amorena Zabalza, Beatriz
Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
author_facet Reina, Ramsés
Glaria, Idoia
Benavides, Julio
Andrés, Ximena de
Crespo, Helena
Solano Goñi, Cristina
Pérez Pérez, Valentín
Luján, Lluís
Pérez, Marta M.
Pérez de la Lastra, José María
Rosati, Sergio
Blacklaws, Barbara
Harkiss, Gordon D.
Andrés, Damián F. de
Amorena Zabalza, Beatriz
author_sort Reina, Ramsés
title Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
title_short Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
title_full Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
title_fullStr Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
title_full_unstemmed Association of CD80 and CD86 expression levels with disease status of Visna/Maedi virus infected sheep
title_sort association of cd80 and cd86 expression levels with disease status of visna/maedi virus infected sheep
publisher Mary Ann Liebert
publishDate 2007-12-25
url http://hdl.handle.net/10261/100092
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