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      Non-specific Effect of Vaccines: Immediate Protection against Respiratory Syncytial Virus Infection by a Live Attenuated Influenza Vaccine

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          Abstract

          The non-specific effects (NSEs) of vaccines have been discussed for their potential long-term beneficial effects beyond direct protection against a specific pathogen. Cold-adapted, live attenuated influenza vaccine (CAIV) induces local innate immune responses that provide a broad range of antiviral immunity. Herein, we examined whether X-31ca, a donor virus for CAIVs, provides non-specific cross-protection against respiratory syncytial virus (RSV). The degree of RSV replication was significantly reduced when X-31ca was administered before RSV infection without any RSV-specific antibody responses. The vaccination induced an immediate release of cytokines and infiltration of leukocytes into the respiratory tract, moderating the immune perturbation caused by RSV infection. The potency of protection against RSV challenge was significantly reduced in TLR3 -/- TLR7 -/- mice, confirming that the TLR3/7 signaling pathways are necessary for the observed immediate and short-term protection. The results suggest that CAIVs provide short-term, non-specific protection against genetically unrelated respiratory pathogens. The additional benefits of CAIVs in mitigating acute respiratory infections for which vaccines are not yet available need to be assessed in future studies.

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          Innate antiviral responses by means of TLR7-mediated recognition of single-stranded RNA.

          Interferons (IFNs) are critical for protection from viral infection, but the pathways linking virus recognition to IFN induction remain poorly understood. Plasmacytoid dendritic cells produce vast amounts of IFN-alpha in response to the wild-type influenza virus. Here, we show that this requires endosomal recognition of influenza genomic RNA and signaling by means of Toll-like receptor 7 (TLR7) and MyD88. Single-stranded RNA (ssRNA) molecules of nonviral origin also induce TLR7-dependent production of inflammatory cytokines. These results identify ssRNA as a ligand for TLR7 and suggest that cells of the innate immune system sense endosomal ssRNA to detect infection by RNA viruses.
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            Innate immunity to influenza virus infection.

            Influenza viruses are a major pathogen of both humans and animals. Recent studies using gene-knockout mice have led to an in-depth understanding of the innate sensors that detect influenza virus infection in a variety of cell types. Signalling downstream of these sensors induces distinct sets of effector mechanisms that block virus replication and promote viral clearance by inducing innate and adaptive immune responses. In this Review, we discuss the various ways in which the innate immune system uses pattern recognition receptors to detect and respond to influenza virus infection. We consider whether the outcome of innate sensor stimulation promotes antiviral resistance or disease tolerance, and propose rational treatment strategies for the acute respiratory disease that is caused by influenza virus infection.
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              Plasmacytoid dendritic cells in immunity.

              Human and mouse plasmacytoid dendritic cells have been shown to correspond to a specialized cell population that produces large amounts of type I interferons in response to viruses, the so-called natural interferon-producing cells. As a result, intensive investigation is now focused on the potential functions of plasmacytoid dendritic cells in both innate and adaptive immunity. Here we review recent progress on the characterization of plasmacytoid dendritic cell origin, development, migration and function in immunity and tolerance, as well as their effect on human diseases.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                31 January 2018
                2018
                : 9
                : 83
                Affiliations
                [1] 1Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University , Seoul, South Korea
                [2] 2Graduate School of Pharmaceutical Sciences, Ewha Womans University , Seoul, South Korea
                [3] 3Department of Biomedical Sciences, Wide River Institute of Immunology, Seoul National University College of Medicine , Seoul, South Korea
                [4] 4Vaccine Translational Research Center, Yonsei University , Seoul, South Korea
                Author notes

                Edited by: Francois Villinger, University of Louisiana at Lafayette, United States

                Reviewed by: Jodi L. McGill, Kansas State University, United States; Hadi M. Yassine, Qatar University, Qatar

                *Correspondence: Baik L. Seong, blseong@ 123456yonsei.ac.kr

                These authors have contributed equally to this work.

                This article was submitted to Virology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2018.00083
                5797773
                29445364
                f132b7af-910b-40f2-ab27-34b1a9dd5dc1
                Copyright © 2018 Lee, Lee, Jang, Seo, Chang and Seong.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 September 2017
                : 12 January 2018
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 54, Pages: 11, Words: 0
                Funding
                Funded by: Ministry of Health and Welfare 10.13039/100008903
                Award ID: HI13C0826
                Funded by: Ministry of Agriculture, Food and Rural Affairs 10.13039/501100003624
                Award ID: MAFRA; 716002-7
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                non-specific effects,cold-adapted live attenuated influenza vaccine,rsv,innate immunity,cross-protection,toll-like receptor

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