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Immune exhaustion during chronic infections in cattle

Recently, dysfunction of antigen-specific T cells is well documented as T-cell exhaustion and has been defined by the loss of effector functions during chronic infections and cancer in human. The exhausted T cells are characterized phenotypically by the surface expression of immunoinhibitory recepto...

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Autores principales: KONNAI, Satoru, MURATA, Shiro, OHASHI, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289228/
https://www.ncbi.nlm.nih.gov/pubmed/27725355
http://dx.doi.org/10.1292/jvms.16-0354
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author KONNAI, Satoru
MURATA, Shiro
OHASHI, Kazuhiko
author_facet KONNAI, Satoru
MURATA, Shiro
OHASHI, Kazuhiko
author_sort KONNAI, Satoru
collection PubMed
description Recently, dysfunction of antigen-specific T cells is well documented as T-cell exhaustion and has been defined by the loss of effector functions during chronic infections and cancer in human. The exhausted T cells are characterized phenotypically by the surface expression of immunoinhibitory receptors, such as programmed death 1 (PD-1), lymphocyte activation gene 3 (LAG-3), T-cell immunoglobulin and mucin domain-containing protein 3 (Tim-3) and cytotoxic T-lymphocyte antigen 4 (CTLA-4). However, there is still a fundamental lack of knowledge about the immunoinhibitory receptors in the fields of veterinary medicine. In particular, very little is known about mechanism of T cell dysfunction in chronic infection in cattle. Recent our studies have revealed that immunoinhibitory molecules including PD-1/ programmed death-ligand 1 (PD-L1) play critical roles in immune exhaustion and disease progression in case of bovine leukemia virus (BLV) infection, Johne’s disease and bovine anaplasmosis. This review includes some recent data from us.
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spelling pubmed-52892282017-02-08 Immune exhaustion during chronic infections in cattle KONNAI, Satoru MURATA, Shiro OHASHI, Kazuhiko J Vet Med Sci Immunology Recently, dysfunction of antigen-specific T cells is well documented as T-cell exhaustion and has been defined by the loss of effector functions during chronic infections and cancer in human. The exhausted T cells are characterized phenotypically by the surface expression of immunoinhibitory receptors, such as programmed death 1 (PD-1), lymphocyte activation gene 3 (LAG-3), T-cell immunoglobulin and mucin domain-containing protein 3 (Tim-3) and cytotoxic T-lymphocyte antigen 4 (CTLA-4). However, there is still a fundamental lack of knowledge about the immunoinhibitory receptors in the fields of veterinary medicine. In particular, very little is known about mechanism of T cell dysfunction in chronic infection in cattle. Recent our studies have revealed that immunoinhibitory molecules including PD-1/ programmed death-ligand 1 (PD-L1) play critical roles in immune exhaustion and disease progression in case of bovine leukemia virus (BLV) infection, Johne’s disease and bovine anaplasmosis. This review includes some recent data from us. The Japanese Society of Veterinary Science 2016-10-08 2017-01 /pmc/articles/PMC5289228/ /pubmed/27725355 http://dx.doi.org/10.1292/jvms.16-0354 Text en ©2017 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Immunology
KONNAI, Satoru
MURATA, Shiro
OHASHI, Kazuhiko
Immune exhaustion during chronic infections in cattle
title Immune exhaustion during chronic infections in cattle
title_full Immune exhaustion during chronic infections in cattle
title_fullStr Immune exhaustion during chronic infections in cattle
title_full_unstemmed Immune exhaustion during chronic infections in cattle
title_short Immune exhaustion during chronic infections in cattle
title_sort immune exhaustion during chronic infections in cattle
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289228/
https://www.ncbi.nlm.nih.gov/pubmed/27725355
http://dx.doi.org/10.1292/jvms.16-0354
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