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      Rapid and Efficient Clearance of Blood-borne Virus by Liver Sinusoidal Endothelium

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          Abstract

          The liver removes quickly the great bulk of virus circulating in blood, leaving only a small fraction to infect the host, in a manner characteristic of each virus. The scavenger cells of the liver sinusoids are implicated, but the mechanism is entirely unknown. Here we show, borrowing a mouse model of adenovirus clearance, that nearly all infused adenovirus is cleared by the liver sinusoidal endothelial cell (LSEC). Using refined immunofluorescence microscopy techniques for distinguishing macrophages and endothelial cells in fixed liver, and identifying virus by two distinct physicochemical methods, we localized adenovirus 1 minute after infusion mainly to the LSEC (∼90%), finding ∼10% with Kupffer cells (KC) and none with hepatocytes. Electron microscopy confirmed our results. In contrast with much prior work claiming the main scavenger to be the KC, our results locate the clearance mechanism to the LSEC and identify this cell as a key site of antiviral activity.

          Author Summary

          The liver has long been known as the garbage dump of the body, capable of rapidly removing hazardous pathogens and useless particles from the blood stream, thereby protecting the host. The only cell doing the removal has been thought to be the liver's macrophages. This is likely true for larger particles such as bacteria. But for smaller particles the size of virus or small antibody-antigen complexes, macrophages are probably not the cell responsible for the bulk of removal. We suggest, rather, it is the endothelial cell of the liver's blood circulatory system that takes up and destroys the majority of virus, doing so quickly (minutes) and extensively (>90%), leaving only a small fraction of circulating virus to infect the body in ways peculiar to each virus. To test this possibility, we infused mice intravenously with a harmless common cold virus and tracked its destination by molecular and microscopy methods. Affirming our conjecture, we found that ∼90% of the infused virus homed to the endothelium of the liver and ∼10% went to its macrophages. These data support a unique role, generally underappreciated, for the liver endothelium in viral clearance.

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          Most cited references36

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          Enhanced infection of liver sinusoidal endothelial cells in a mouse model of antibody-induced severe dengue disease.

          Dengue virus (DENV) causes disease ranging from dengue fever (DF), a self-limited febrile illness, to the potentially lethal dengue hemorrhagic fever and dengue shock syndrome (DHF/DSS). DHF/DSS usually occurs in patients who have acquired DENV-reactive antibodies prior to infection, either from a previous infection with a heterologous DENV serotype or from an immune mother. Hence, it has been hypothesized that subneutralizing levels of antibodies exacerbate disease, a phenomenon termed antibody-dependent enhancement (ADE). However, given the lack of suitable animal models for DENV infection, the mechanism of ADE and its contribution to pathology remain elusive. Here we demonstrate in mice that DENV-specific antibodies can sufficiently increase severity of disease so that a mostly nonlethal illness becomes a fatal disease resembling human DHF/DSS. Antibodies promote massive infection of liver sinusoidal endothelial cells (LSECs), resulting in increased systemic levels of virus. Thus, a subprotective humoral response may, under some circumstances, have pathological consequences. 2010 Elsevier Inc. All rights reserved.
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            The mononuclear phagocyte system: a new classification of macrophages, monocytes, and their precursor cells.

            There have been many attempts in the past to classify phagocytic mononuclear cells and to define the cell system they are considered to form-among these being the "macrophage system" of Metchnikoff, the "reticulo-endothelial system" of Aschoff, and the "reticulo-histiocyte system" proposed by Volterra and reintroduced by Thomas. None of these is entirely adequate in the light of present knowledge. In 1969, therefore, a group of workers proposed a new classification of all highly phagocytic mononuclear cells and their precursors in what they termed the "mononuclear phagocyte system". This system includes the promonocytes and their precursors in the bone marrow, the monocytes in the peripheral blood, and the macrophages in the tissues. Subsequent consultation with numerous other specialists throughout the world led to a certain number of changes in this classification, which is now proposed in revised form.Inclusion of cells in the "mononuclear phagocyte system" is based on similarities in the morphology, function, origin, and kinetics of the phagocytes. By these criteria reticular cells, dendritic cells, endothelial cells, and fibroblasts (fibrocytes) are excluded. The proponents point out that as new knowledge is acquired modifications may have to be made, certain cells being added to or removed from the new classification.
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              Blood clearance rates of adenovirus type 5 in mice.

              Persistence of adenovirus type 5 in blood has implications for the pathogenicity of the virus infection and for the use of this virus in oncolysis and gene therapy. In this study, the kinetics of adenovirus clearance from blood in mice has been evaluated. After a single inoculation of concentrated virus into the vena cava, virus half-life was less than 2 min. Depletion of Kupffer cells (KC) resulted in increased viraemia. After tail-vein injection, virus and latex beads co-localized within KC. An important factor in clearance by KC is the negative charge of particles. Deletion of the hexon hypervariable region 1 acidic stretch decreased the negative charge of the virion but it did not increase blood persistence. Coating with PEG ('PEGylation') reduced the clearance rate but also reduced infectivity.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Pathog
                plos
                plospath
                PLoS Pathogens
                Public Library of Science (San Francisco, USA )
                1553-7366
                1553-7374
                September 2011
                September 2011
                29 September 2011
                : 7
                : 9
                : e1002281
                Affiliations
                [1 ]Department of Internal Medicine, The Ohio State University, Columbus, Ohio, United States of America
                [2 ]Harvard School of Public Health, Boston, Massachusetts, United States of America
                [3 ]Department of Pediatrics, The Ohio State University, Columbus, Ohio, United States of America
                [4 ]Center for Gene Therapy, Research Institute at Nationwide Children's Hospital, Columbus, Ohio, United States of America
                [5 ]Department of Physiology and Cell Biology, The Ohio State University, Columbus, Ohio, United States of America
                Harvard University, United States of America
                Author notes

                Conceived and designed the experiments: LPG SM JK KRC JMR CLA. Performed the experiments: LPG SM JMR. Analyzed the data: LPG JK KRC JMR CLA. Contributed reagents/materials/analysis tools: JMR KRC. Wrote the paper: LPG CLA.

                Article
                PPATHOGENS-D-11-01154
                10.1371/journal.ppat.1002281
                3182912
                21980295
                e5aecb39-57b9-4ac8-b175-004b1ebfed46
                Ganesan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 2 June 2011
                : 7 August 2011
                Page count
                Pages: 11
                Categories
                Research Article
                Biology
                Immunology
                Immunologic Techniques
                Immunoassays
                Immunofluorescence
                Immunohistochemical Analysis
                Immune Cells
                Immune Response
                Microbiology
                Virology
                Viral Transmission and Infection
                Viral Clearance
                Viral Vectors
                Animal Models of Infection
                Antivirals
                Immunodeficiency Viruses
                Mechanisms of Resistance and Susceptibility
                Viral Immune Evasion
                Molecular Cell Biology
                Cellular Types

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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