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Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses
Lentiviruses are infectious agents of a number of animal species, including sheep, goats, horses, monkeys, cows, and cats, in addition to humans. As in the human case, the host immune response fails to control the establishment of chronic persistent infection that finally leads to a specific disease...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116218/ https://www.ncbi.nlm.nih.gov/pubmed/30126090 http://dx.doi.org/10.3390/v10080435 |
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author | de Pablo-Maiso, Lorena Doménech, Ana Echeverría, Irache Gómez-Arrebola, Carmen de Andrés, Damián Rosati, Sergio Gómez-Lucia, Esperanza Reina, Ramsés |
author_facet | de Pablo-Maiso, Lorena Doménech, Ana Echeverría, Irache Gómez-Arrebola, Carmen de Andrés, Damián Rosati, Sergio Gómez-Lucia, Esperanza Reina, Ramsés |
author_sort | de Pablo-Maiso, Lorena |
collection | PubMed |
description | Lentiviruses are infectious agents of a number of animal species, including sheep, goats, horses, monkeys, cows, and cats, in addition to humans. As in the human case, the host immune response fails to control the establishment of chronic persistent infection that finally leads to a specific disease development. Despite intensive research on the development of lentivirus vaccines, it is still not clear which immune responses can protect against infection. Viral mutations resulting in escape from T-cell or antibody-mediated responses are the basis of the immune failure to control the infection. The innate immune response provides the first line of defense against viral infections in an antigen-independent manner. Antiviral innate responses are conducted by dendritic cells, macrophages, and natural killer cells, often targeted by lentiviruses, and intrinsic antiviral mechanisms exerted by all cells. Intrinsic responses depend on the recognition of the viral pathogen-associated molecular patterns (PAMPs) by pathogen recognition receptors (PRRs), and the signaling cascades leading to an antiviral state by inducing the expression of antiviral proteins, including restriction factors. This review describes the latest advances on innate immunity related to the infection by animal lentiviruses, centered on small ruminant lentiviruses (SRLV), equine infectious anemia virus (EIAV), and feline (FIV) and bovine immunodeficiency viruses (BIV), specifically focusing on the antiviral role of the major restriction factors described thus far. |
format | Online Article Text |
id | pubmed-6116218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61162182018-08-31 Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses de Pablo-Maiso, Lorena Doménech, Ana Echeverría, Irache Gómez-Arrebola, Carmen de Andrés, Damián Rosati, Sergio Gómez-Lucia, Esperanza Reina, Ramsés Viruses Review Lentiviruses are infectious agents of a number of animal species, including sheep, goats, horses, monkeys, cows, and cats, in addition to humans. As in the human case, the host immune response fails to control the establishment of chronic persistent infection that finally leads to a specific disease development. Despite intensive research on the development of lentivirus vaccines, it is still not clear which immune responses can protect against infection. Viral mutations resulting in escape from T-cell or antibody-mediated responses are the basis of the immune failure to control the infection. The innate immune response provides the first line of defense against viral infections in an antigen-independent manner. Antiviral innate responses are conducted by dendritic cells, macrophages, and natural killer cells, often targeted by lentiviruses, and intrinsic antiviral mechanisms exerted by all cells. Intrinsic responses depend on the recognition of the viral pathogen-associated molecular patterns (PAMPs) by pathogen recognition receptors (PRRs), and the signaling cascades leading to an antiviral state by inducing the expression of antiviral proteins, including restriction factors. This review describes the latest advances on innate immunity related to the infection by animal lentiviruses, centered on small ruminant lentiviruses (SRLV), equine infectious anemia virus (EIAV), and feline (FIV) and bovine immunodeficiency viruses (BIV), specifically focusing on the antiviral role of the major restriction factors described thus far. MDPI 2018-08-17 /pmc/articles/PMC6116218/ /pubmed/30126090 http://dx.doi.org/10.3390/v10080435 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review de Pablo-Maiso, Lorena Doménech, Ana Echeverría, Irache Gómez-Arrebola, Carmen de Andrés, Damián Rosati, Sergio Gómez-Lucia, Esperanza Reina, Ramsés Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title | Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title_full | Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title_fullStr | Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title_full_unstemmed | Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title_short | Prospects in Innate Immune Responses as Potential Control Strategies against Non-Primate Lentiviruses |
title_sort | prospects in innate immune responses as potential control strategies against non-primate lentiviruses |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116218/ https://www.ncbi.nlm.nih.gov/pubmed/30126090 http://dx.doi.org/10.3390/v10080435 |
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