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HIV-1 Is a Poor Inducer of Innate Immune Responses

Effective host immune responses against viral infection rely on the detection of the virus, activation of downstream signaling pathways, and the secretion of interferons (IFNs) and other cytokines. Many viruses can potently stimulate these responses, whereas the immune response against human immunod...

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Detalles Bibliográficos
Autores principales: Cingöz, Oya, Goff, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372803/
https://www.ncbi.nlm.nih.gov/pubmed/30755516
http://dx.doi.org/10.1128/mBio.02834-18
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author Cingöz, Oya
Goff, Stephen P.
author_facet Cingöz, Oya
Goff, Stephen P.
author_sort Cingöz, Oya
collection PubMed
description Effective host immune responses against viral infection rely on the detection of the virus, activation of downstream signaling pathways, and the secretion of interferons (IFNs) and other cytokines. Many viruses can potently stimulate these responses, whereas the immune response against human immunodeficiency virus type 1 (HIV-1) remains relatively less well characterized. Here we show that HIV-1 infection with reporter viruses does not activate sensing pathways in cell lines and primary cells that are otherwise responsive to foreign nucleic acids. After entry into cells, reverse transcription and reporter expression occur without the virus ever being detected by cellular sensors or stimulating an interferon response. Using multiple methods, including the use of reporter cell lines for type I IFN and NF-κB pathway activation, quantifying mRNA levels for IFN-stimulated genes (ISGs), and assaying for markers of innate immune activation, we show that single-round pseudotyped HIV-1-based reporter viruses fail to induce innate immune responses.
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spelling pubmed-63728032019-02-22 HIV-1 Is a Poor Inducer of Innate Immune Responses Cingöz, Oya Goff, Stephen P. mBio Observation Effective host immune responses against viral infection rely on the detection of the virus, activation of downstream signaling pathways, and the secretion of interferons (IFNs) and other cytokines. Many viruses can potently stimulate these responses, whereas the immune response against human immunodeficiency virus type 1 (HIV-1) remains relatively less well characterized. Here we show that HIV-1 infection with reporter viruses does not activate sensing pathways in cell lines and primary cells that are otherwise responsive to foreign nucleic acids. After entry into cells, reverse transcription and reporter expression occur without the virus ever being detected by cellular sensors or stimulating an interferon response. Using multiple methods, including the use of reporter cell lines for type I IFN and NF-κB pathway activation, quantifying mRNA levels for IFN-stimulated genes (ISGs), and assaying for markers of innate immune activation, we show that single-round pseudotyped HIV-1-based reporter viruses fail to induce innate immune responses. American Society for Microbiology 2019-02-12 /pmc/articles/PMC6372803/ /pubmed/30755516 http://dx.doi.org/10.1128/mBio.02834-18 Text en Copyright © 2019 Cingöz and Goff. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Observation
Cingöz, Oya
Goff, Stephen P.
HIV-1 Is a Poor Inducer of Innate Immune Responses
title HIV-1 Is a Poor Inducer of Innate Immune Responses
title_full HIV-1 Is a Poor Inducer of Innate Immune Responses
title_fullStr HIV-1 Is a Poor Inducer of Innate Immune Responses
title_full_unstemmed HIV-1 Is a Poor Inducer of Innate Immune Responses
title_short HIV-1 Is a Poor Inducer of Innate Immune Responses
title_sort hiv-1 is a poor inducer of innate immune responses
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372803/
https://www.ncbi.nlm.nih.gov/pubmed/30755516
http://dx.doi.org/10.1128/mBio.02834-18
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