Tick-borne flaviviruses: dissecting host immune responses and virus countermeasures
The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus , includes a number of important human pathogens that cause serious neurological illnesses and hemorrhagic fevers. These viruses pose a significant public health problem due to high rates of morbidity and mortality, their eme...
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Published in | Immunologic research Vol. 43; no. 1-3; pp. 172 - 186 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Humana Press Inc
2009
Springer Nature B.V |
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Abstract | The tick-borne encephalitis (TBE) serocomplex of viruses, genus
Flavivirus
, includes a number of important human pathogens that cause serious neurological illnesses and hemorrhagic fevers. These viruses pose a significant public health problem due to high rates of morbidity and mortality, their emergence to new geographic areas, and the recent rise in the incidence of human infections. The most notable member of the TBE serocomplex is tick-borne encephalitis virus (TBEV), a neurotropic flavivirus that causes debilitating and sometimes fatal encephalitis. Although effective prophylactic anti-TBEV vaccines have been developed, there is currently no specific treatment for infection. To identify new targets for therapeutical intervention, it is imperative to understand interactions between TBEV and the host immune response to infection. Interferon (IFN) has a critical role in controlling flavivirus replication. Dendritic cells (DCs) represent an early target of TBEV infection and are major producers of IFN. Thus, interactions between DCs, IFN responses, and the virus are likely to substantially influence the outcome of infection. Early IFN and DC responses are modulated not only by the virus, but also by the tick vector and immunomodulatory compounds of tick saliva inoculated with virus into the skin. Our laboratory is examining interactions between the triad of virus, tick vector, and mammalian host that contribute to the pathogenesis of tick-borne flaviviruses. This work will provide a more detailed understanding of early events in virus infection and their impact on flavivirus pathogenesis. |
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AbstractList | The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus, includes a number of important human pathogens that cause serious neurological illnesses and hemorrhagic fevers. These viruses pose a significant public health problem due to high rates of morbidity and mortality, their emergence to new geographic areas, and the recent rise in the incidence of human infections. The most notable member of the TBE serocomplex is tick-borne encephalitis virus (TBEV), a neurotropic flavivirus that causes debilitating and sometimes fatal encephalitis. Although effective prophylactic anti-TBEV vaccines have been developed, there is currently no specific treatment for infection. To identify new targets for therapeutical intervention, it is imperative to understand interactions between TBEV and the host immune response to infection. Interferon (IFN) has a critical role in controlling flavivirus replication. Dendritic cells (DCs) represent an early target of TBEV infection and are major producers of IFN. Thus, interactions between DCs, IFN responses, and the virus are likely to substantially influence the outcome of infection. Early IFN and DC responses are modulated not only by the virus, but also by the tick vector and immunomodulatory compounds of tick saliva inoculated with virus into the skin. Our laboratory is examining interactions between the triad of virus, tick vector, and mammalian host that contribute to the pathogenesis of tick-borne flaviviruses. This work will provide a more detailed understanding of early events in virus infection and their impact on flavivirus pathogenesis. Issue Title: National Institutes of Health/NIAID special issue The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus, includes a number of important human pathogens that cause serious neurological illnesses and hemorrhagic fevers. These viruses pose a significant public health problem due to high rates of morbidity and mortality, their emergence to new geographic areas, and the recent rise in the incidence of human infections. The most notable member of the TBE serocomplex is tick-borne encephalitis virus (TBEV), a neurotropic flavivirus that causes debilitating and sometimes fatal encephalitis. Although effective prophylactic anti-TBEV vaccines have been developed, there is currently no specific treatment for infection. To identify new targets for therapeutical intervention, it is imperative to understand interactions between TBEV and the host immune response to infection. Interferon (IFN) has a critical role in controlling flavivirus replication. Dendritic cells (DCs) represent an early target of TBEV infection and are major producers of IFN. Thus, interactions between DCs, IFN responses, and the virus are likely to substantially influence the outcome of infection. Early IFN and DC responses are modulated not only by the virus, but also by the tick vector and immunomodulatory compounds of tick saliva inoculated with virus into the skin. Our laboratory is examining interactions between the triad of virus, tick vector, and mammalian host that contribute to the pathogenesis of tick-borne flaviviruses. This work will provide a more detailed understanding of early events in virus infection and their impact on flavivirus pathogenesis. [PUBLICATION ABSTRACT] The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus , includes a number of important human pathogens that cause serious neurological illnesses and hemorrhagic fevers. These viruses pose a significant public health problem due to high rates of morbidity and mortality, their emergence to new geographic areas, and the recent rise in the incidence of human infections. The most notable member of the TBE serocomplex is tick-borne encephalitis virus (TBEV), a neurotropic flavivirus that causes debilitating and sometimes fatal encephalitis. Although effective prophylactic anti-TBEV vaccines have been developed, there is currently no specific treatment for infection. To identify new targets for therapeutical intervention, it is imperative to understand interactions between TBEV and the host immune response to infection. Interferon (IFN) has a critical role in controlling flavivirus replication. Dendritic cells (DCs) represent an early target of TBEV infection and are major producers of IFN. Thus, interactions between DCs, IFN responses, and the virus are likely to substantially influence the outcome of infection. Early IFN and DC responses are modulated not only by the virus, but also by the tick vector and immunomodulatory compounds of tick saliva inoculated with virus into the skin. Our laboratory is examining interactions between the triad of virus, tick vector, and mammalian host that contribute to the pathogenesis of tick-borne flaviviruses. This work will provide a more detailed understanding of early events in virus infection and their impact on flavivirus pathogenesis. |
Author | Robertson, Shelly J. Bloom, Marshall E. Mitzel, Dana N. Taylor, R. Travis Best, Sonja M. |
Author_xml | – sequence: 1 givenname: Shelly J. surname: Robertson fullname: Robertson, Shelly J. organization: Laboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health – sequence: 2 givenname: Dana N. surname: Mitzel fullname: Mitzel, Dana N. organization: Laboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health – sequence: 3 givenname: R. Travis surname: Taylor fullname: Taylor, R. Travis organization: Laboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health – sequence: 4 givenname: Sonja M. surname: Best fullname: Best, Sonja M. organization: Laboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health – sequence: 5 givenname: Marshall E. surname: Bloom fullname: Bloom, Marshall E. email: mbloom@niaid.nih.gov organization: Laboratory of Virology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18841330$$D View this record in MEDLINE/PubMed |
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Keywords | tick vector Interferon antagonism Tick-borne flavivirus Dendritic cells |
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Snippet | The tick-borne encephalitis (TBE) serocomplex of viruses, genus
Flavivirus
, includes a number of important human pathogens that cause serious neurological... The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus, includes a number of important human pathogens that cause serious neurological... Issue Title: National Institutes of Health/NIAID special issue The tick-borne encephalitis (TBE) serocomplex of viruses, genus Flavivirus, includes a number of... |
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SubjectTerms | Allergology Animals Biomedical and Life Sciences Biomedicine Dendritic Cells - immunology Dendritic Cells - metabolism Dendritic Cells - virology Disease Vectors Encephalitis Viruses, Tick-Borne - immunology Encephalitis Viruses, Tick-Borne - pathogenicity Encephalitis, Tick-Borne - immunology Encephalitis, Tick-Borne - transmission Encephalitis, Tick-Borne - virology Flavivirus Humans Immunity, Innate Immunology Interferon Interferons - immunology Interferons - metabolism Internal Medicine Ixodidae Janus Kinases - immunology Janus Kinases - metabolism Medicine/Public Health Neurological disorders Parasites Pathogens Receptors, Pattern Recognition - immunology Receptors, Pattern Recognition - metabolism Signal Transduction - immunology STAT Transcription Factors - immunology STAT Transcription Factors - metabolism Tick-borne encephalitis virus Ticks - virology Viral Envelope Proteins - immunology Viral Envelope Proteins - metabolism Viral Nonstructural Proteins - immunology Viral Nonstructural Proteins - metabolism Viral Vaccines - immunology Viruses |
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