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Human erythrocytes bind and inactivate type 5 adenovirus by presenting Coxsackie virus-adenovirus receptor and complement receptor 1

  1. 1.
    SYSNO ASEP0322079
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHuman erythrocytes bind and inactivate type 5 adenovirus by presenting Coxsackie virus-adenovirus receptor and complement receptor 1
    TitleLidské erytrocyty obsahující Coxsakie virus-adenovirus receptor a komplement receptor 1 váží a inaktivují adenovirus typu 5
    Author(s) Carlisle, R. C. (GB)
    Di, Y. (GB)
    Cerny, A. M. (US)
    Sonnen, A. F. P. (GB)
    Sim, R. B. (GB)
    Green, N. K. (GB)
    Šubr, Vladimír (UMCH-V) RID, ORCID
    Ulbrich, Karel (UMCH-V) RID
    Gilbert, R. J. C. (GB)
    Fisher, K. D. (GB)
    Finberg, R. W. (US)
    Seymour, L. W. (GB)
    Source TitleBlood. - : American Society of Hematology - ISSN 0006-4971
    Roč. 113, č. 9 (2009), s. 1909-1918
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordsadenovirus ; erythrocyte ; complement receptor 1
    Subject RIVCD - Macromolecular Chemistry
    CEZAV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000263723700008
    DOI10.1182/blood-2008-09-178459
    AnnotationHere we report the unexpected presence of high affinity Ad5 receptors on human erythrocytes, which may function as decoys to protect organism against systemic virus infection, perhaps representing an evolutionary response to the challenge of widespread adenovirus pathology. Here we define the mechanism of Ad5 binding to human erythrocytes and document presentation of Coxsackie virus-adenovirus receptor (CAR) and complement receptor 1 (CR1), which efficiently sequester Ad5 in the absence and presence of anti-Ad5 antibodies, respectively. We demonstrate that erythrocyte binding alters the blood circulation profile of intravenously administered Ad5 and dramatically reduces its extravasation and infectivity. "Stealthing" of Ad5 using hydrophilic polymers may enable circumvention of these natural virus traps.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2009
Number of the records: 1  

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