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Myeloid Cell Arg1 Inhibits Control of Arthritogenic Alphavirus Infection by Suppressing Antiviral T Cells
by
McCarthy, Mary K.
, Ng, Lisa F. P.
, Tan, Jeslin J. L.
, Morrison, Thomas E.
, Her, Zhisheng
, Burrack, Kristina S.
, Berger, Jennifer N.
in
Adoptive Transfer
/ Alphavirus Infections - immunology
/ Animals
/ Antiviral agents
/ Arginase - immunology
/ Australia
/ Biological response modifiers
/ Biomedical research
/ Blotting, Western
/ Chikungunya Fever - immunology
/ Chikungunya virus
/ Chronic illnesses
/ Complications and side effects
/ Development and progression
/ Disease
/ Dosage and administration
/ Drug therapy
/ Epidemics
/ Experiments
/ Flow Cytometry
/ Gene expression
/ Health aspects
/ Humans
/ Infections
/ Inflammation
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Mosquitoes
/ Myeloid Cells - immunology
/ Pain
/ Patient outcomes
/ Polymerase Chain Reaction
/ Rodents
/ Ross River virus - immunology
/ Singapore
/ Spleen
/ T-Lymphocytes - immunology
/ Viral Load - immunology
/ Virology
/ Viruses
2015
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Myeloid Cell Arg1 Inhibits Control of Arthritogenic Alphavirus Infection by Suppressing Antiviral T Cells
by
McCarthy, Mary K.
, Ng, Lisa F. P.
, Tan, Jeslin J. L.
, Morrison, Thomas E.
, Her, Zhisheng
, Burrack, Kristina S.
, Berger, Jennifer N.
in
Adoptive Transfer
/ Alphavirus Infections - immunology
/ Animals
/ Antiviral agents
/ Arginase - immunology
/ Australia
/ Biological response modifiers
/ Biomedical research
/ Blotting, Western
/ Chikungunya Fever - immunology
/ Chikungunya virus
/ Chronic illnesses
/ Complications and side effects
/ Development and progression
/ Disease
/ Dosage and administration
/ Drug therapy
/ Epidemics
/ Experiments
/ Flow Cytometry
/ Gene expression
/ Health aspects
/ Humans
/ Infections
/ Inflammation
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Mosquitoes
/ Myeloid Cells - immunology
/ Pain
/ Patient outcomes
/ Polymerase Chain Reaction
/ Rodents
/ Ross River virus - immunology
/ Singapore
/ Spleen
/ T-Lymphocytes - immunology
/ Viral Load - immunology
/ Virology
/ Viruses
2015
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Myeloid Cell Arg1 Inhibits Control of Arthritogenic Alphavirus Infection by Suppressing Antiviral T Cells
by
McCarthy, Mary K.
, Ng, Lisa F. P.
, Tan, Jeslin J. L.
, Morrison, Thomas E.
, Her, Zhisheng
, Burrack, Kristina S.
, Berger, Jennifer N.
in
Adoptive Transfer
/ Alphavirus Infections - immunology
/ Animals
/ Antiviral agents
/ Arginase - immunology
/ Australia
/ Biological response modifiers
/ Biomedical research
/ Blotting, Western
/ Chikungunya Fever - immunology
/ Chikungunya virus
/ Chronic illnesses
/ Complications and side effects
/ Development and progression
/ Disease
/ Dosage and administration
/ Drug therapy
/ Epidemics
/ Experiments
/ Flow Cytometry
/ Gene expression
/ Health aspects
/ Humans
/ Infections
/ Inflammation
/ Lymphocyte Activation - immunology
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Mosquitoes
/ Myeloid Cells - immunology
/ Pain
/ Patient outcomes
/ Polymerase Chain Reaction
/ Rodents
/ Ross River virus - immunology
/ Singapore
/ Spleen
/ T-Lymphocytes - immunology
/ Viral Load - immunology
/ Virology
/ Viruses
2015
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Myeloid Cell Arg1 Inhibits Control of Arthritogenic Alphavirus Infection by Suppressing Antiviral T Cells
Journal Article
Myeloid Cell Arg1 Inhibits Control of Arthritogenic Alphavirus Infection by Suppressing Antiviral T Cells
2015
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Overview
Arthritogenic alphaviruses, including Ross River virus (RRV) and chikungunya virus (CHIKV), are responsible for explosive epidemics involving millions of cases. These mosquito-transmitted viruses cause inflammation and injury in skeletal muscle and joint tissues that results in debilitating pain. We previously showed that arginase 1 (Arg1) was highly expressed in myeloid cells in the infected and inflamed musculoskeletal tissues of RRV- and CHIKV-infected mice, and specific deletion of Arg1 from myeloid cells resulted in enhanced viral control. Here, we show that Arg1, along with other genes associated with suppressive myeloid cells, is induced in PBMCs isolated from CHIKV-infected patients during the acute phase as well as the chronic phase, and that high Arg1 expression levels were associated with high viral loads and disease severity. Depletion of both CD4 and CD8 T cells from RRV-infected Arg1-deficient mice restored viral loads to levels detected in T cell-depleted wild-type mice. Moreover, Arg1-expressing myeloid cells inhibited virus-specific T cells in the inflamed and infected musculoskeletal tissues, but not lymphoid tissues, following RRV infection in mice, including suppression of interferon-γ and CD69 expression. Collectively, these data enhance our understanding of the immune response following arthritogenic alphavirus infection and suggest that immunosuppressive myeloid cells may contribute to the duration or severity of these debilitating infections.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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